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  • 1
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Bioluminescence and Chemiluminescence 1 (1986), S. 11-14 
    ISSN: 0884-3996
    Keywords: Bioluminescent assay ; D-3-hydroxybutyrate ; bacterial luciferase ; Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: An enzymatic assay of D-3-hydroxybutyrate in which the hydroxybutyrate dehydrogenase reaction is coupled to the bacterial oxidoreductase - uciferase system is described. The bioluminescent assay is based on either, end-point, or on initial velocity measurements. This simple and rapid assay requires a single serum sample of 10 μl. Its linear range covers two orders of magnitude from 10-6 mol/I upwards. This assay is suitable for the routine determination of D-3-hydroxybutyrate in human blood with good accuracy.
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  • 2
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    New York : Wiley-Blackwell
    Journal of Bioluminescence and Chemiluminescence 1 (1986), S. 45-45 
    ISSN: 0884-3996
    Keywords: Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
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  • 3
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    New York : Wiley-Blackwell
    Journal of Bioluminescence and Chemiluminescence 1 (1986), S. 46-46 
    ISSN: 0884-3996
    Keywords: Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
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  • 4
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    New York : Wiley-Blackwell
    Journal of Bioluminescence and Chemiluminescence 1 (1986), S. 1-1 
    ISSN: 0884-3996
    Keywords: Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
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  • 5
    Electronic Resource
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    New York : Wiley-Blackwell
    Journal of Bioluminescence and Chemiluminescence 1 (1986), S. 3-10 
    ISSN: 0884-3996
    Keywords: ATP ; foods ; microbiology ; analysis ; Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: The bioluminescent assay of ATP is rapid and simple and may be used as an estimate of microbial numbers. It therefore shows great potential as a technique to provied information on the microbiological quality of a food within a few minutes, in comparison with conventional techniques, which provide results retrospectively. Howver, despite the advantages of speed and senstitivity, no food microbiologists are using the technique for routine quality control and hygiene monitoring. This review seeks to highlight the reasons for this, and to offer some ideas for future research to increase the acceptance of ATP assays within the food industry.
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  • 6
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    New York : Wiley-Blackwell
    Journal of Bioluminescence and Chemiluminescence 1 (1986), S. 29-34 
    ISSN: 0884-3996
    Keywords: Enhanced chemiluminescence ; enzyme immunoassay ; carcinoembryonic antigen ; Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: A conventional colorimetric peroxidase end-point (ortho-phenylenediamine substrate), used in an enzyme immunoassay for carcinoembryonic antigen, employing plastic beads as solid support, has been replaced by a much faster (30 seconds versus 30 minutes) enhanced chemiluminescent assay for the peroxidase label. Para-iodophenol was used to enhance the light emission from the peroxidase catalysed chemiluminescent reaction between luminol and hydrogen peroxide. Values for precision and carcinoembryonic antigen concentration obtained with the chemiluminescent and colorimetric versions of the immunoassay on 62 serum specimens were in good agreement.
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  • 7
    Electronic Resource
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    New York : Wiley-Blackwell
    Journal of Bioluminescence and Chemiluminescence 1 (1986), S. 35-44 
    ISSN: 0884-3996
    Keywords: Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
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  • 8
    Electronic Resource
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    New York : Wiley-Blackwell
    Journal of Bioluminescence and Chemiluminescence 1 (1986), S. 15-27 
    ISSN: 0884-3996
    Keywords: Luminol-dependent chemiluminescence ; polymorphonuclear leucoytes ; unopsonized bacteria ; chemotactic peptide ; myeloperoxidase ; calcium ; Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Optimum conditions were established for the generation and measurement of luminoldependent chemiluminescence (CL) in human polymorphonuclear leucocytes (PMNL) stimulated with a variety of particulate and soluble agents. Several factors had a particular influence on the kinetics of CL stimulated by the chemotactic peptide N-formyl-L-methionyl-L-leucyl-L-phenylalanine (fMLP). Two peaks, both azide-sensitive, were observed at 21°C and 25°C. but these increased in magnitude and merged t o give a single, early peak when the temperature was increased t o 37°C. Pre-exposure of PMNL to a buffer containing calcium was essential for the expression of both phases of fMLP-stimulated CL, while the second peak decreased dramatically if the cells were stored at 4°C for 4 hours before assay. In contrast, storage of PMNL at 4°C for up t o 8 hours in a buffer without divalent cations did not alter the kinetics or magnitude of CL induced by other stimuli, and had the benefit of minimizing the rate of cell aggregation. This study confirms that measurement of luminol-dependent CL in stimulated PMNL is a useful analytical tool, but shows that careful attention t o experimental design is required t o ensure that the observed CL provides a true measure of the parameter under investigation.
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  • 9
    ISSN: 0884-3996
    Keywords: Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
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  • 10
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    New York : Wiley-Blackwell
    Journal of Bioluminescence and Chemiluminescence 1 (1986), S. 59-76 
    ISSN: 0884-3996
    Keywords: Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
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  • 11
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    New York : Wiley-Blackwell
    Journal of Bioluminescence and Chemiluminescence 1 (1986), S. 77-85 
    ISSN: 0884-3996
    Keywords: Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
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  • 12
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    New York : Wiley-Blackwell
    Journal of Bioluminescence and Chemiluminescence 1 (1986), S. 87-145 
    ISSN: 0884-3996
    Keywords: Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
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  • 13
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    New York : Wiley-Blackwell
    Journal of Bioluminescence and Chemiluminescence 1 (1986) 
    ISSN: 0884-3996
    Keywords: Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
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  • 14
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    New York : Wiley-Blackwell
    Journal of Bioluminescence and Chemiluminescence 1 (1986) 
    ISSN: 0884-3996
    Keywords: Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
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  • 15
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    Journal of Bioluminescence and Chemiluminescence 1 (1986), S. 53-58 
    ISSN: 0884-3996
    Keywords: enhanced chemiluminescence ; immunoassay ; allergen ; IgE ; Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: An enhanced chemiluminescent immunoassay is described for the measurement of allergen-specific IgE antibodies. The assay is demonstrated for pollen from four grass species. A comparison was made between results obtained by this method and those obtained by the radioallergosorbent (RAST) procedure; a high degree of correlation (r = 0.95) was found for D. glomerata specific IgE. The assay is rapid and can be carried out in under 1 hour. The advantages of the luminescent assay as compared with the RAST procedure are discussed.
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  • 16
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    New York : Wiley-Blackwell
    Journal of Bioluminescence and Chemiluminescence 1 (1986), S. 47-51 
    ISSN: 0884-3996
    Keywords: ATP ; luciferin-luciferase ; bioluminescent assay ; HLA-typing ; Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: The amount of adenosine triphosphate (ATP) in human lymphocytes was determined using a technique based on light emission from a bioluminescent reaction with luciferin-luciferase. The amount of ATP changed when cells were incubated in the presence of specific HLA antisera and complement. For determination of intracellular ATP a modified method was applied, which was based on reduction of extracellular ATP by the addition of ATPase. The results of titration of an anti-human lymphocyte serum using the bioluminescence assay were in agreement with the results of fluorescence vitality staining. Bioluminescent HLA-determination in 57 cell samples each tested with 5 different antisera also gave good agreement (95.8%) with the conventional method. From these experimental data the calculated ATP content per lymphocyte was 0.135 ± 0.058 pg ATP.
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  • 17
    ISSN: 0173-0835
    Keywords: Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: The relation between the electrophoretic migration velocity and the concentration of the non-ionic detergent Triton X-100 in the buffer was studied by crossed immunoelectrophoresis of hydrophilic and amphiphilic proteins. The migration velocity of hydrophilic human plasma proteins was not affected by the presence of Triton X-100 in the agarose gels in the concentration range of 1-0 % v/v. In contrast, amphiphilic proteins, like the human erythrocyte proteins glycophorin, band 3 protein and acetylcholinesterase, and the plasma high density lipoprotein (HDL) apolipoprotein, showed increasing migration velocity with decreasing detergent concentration in the gels. An increase of 20-80 % was observed for different amphiphilic proteins when the Triton X-100 concentration was lowered from 1 % to 0.03 % v/v. This probably reflects the influence of the size of the bound detergent micelle on the charge density of the protein. Thus, by performing corssed immunoelectrophoresis with different concentrations of Triton X-100 in the first-dimensional gel it is possible to identify amphiphilic proteins. Presence of 1 % v/v Triton X-100 in the second-dimensional gel ensures reliable identification of the precipitates.
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  • 18
    ISSN: 0173-0835
    Keywords: Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: A method for separating fetal hemoglobin Sardinia (AγT, a variant containing threonine in position 75 instead of isoleucine) from normal fetal hemoglobin is described, based on the use of shallow immobilized pH gradients (pH 7.30-7.55). The novelty of the fractionation technique is the direct analysis of intact, native hemoglobin tetramers, while present methods utilize only reverse-phase, high performance liquid chromatography of denatured, heme-free globin chains.
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  • 19
    ISSN: 0173-0835
    Keywords: Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Recently, we described hybrid isoelectric focusing in rehydrated polyacrylamide gels as an analytical procedure which is based on separation in immobilized pH gradients supplemented with low concentrations of carrier ampholytes (Altland and Rossmann, Electrophoresis 1985, 6, 314-325). When using this procedure at various pH ranges, in the presence of reducing agents and carrier ampholytes at different concentrations and from different suppliers, over prolonged time intervals for separation and at various acrylamide concentrations in the gel, liquid exudation has been observed on the gel surface which may result in a confluent liquid layer adversely affecting the final separation pattern. The effect is demonstrated and procedures are described to overcome the phenomenon by adding polyols like glycerol, sorbitol, sucrose or dextrans to the rehydration solution. Comparable effects are achieved when these components are added at the same concentration by weight rather than by moles. The addition of 10 g % Dextran 8 or 20 g % sucrose or sorbitol to the rehydration solution prevents liquid exudation for several hours. These additives are compatible with high concentrations of urea, with reducing agents and with neutral detergent (Triton X-100).
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  • 20
    ISSN: 0173-0835
    Keywords: Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Immobilized pH gradient (IPG) slab gels are conventionally formed by use of two-chamber gradient mixers on pH-neutralized Immobiline mixtures, co-polymerization of the gradient of Immobilines with acrylamide at 50 °C, washing and drying of the gel to its original weight followed by pre-electrophoresis before applying the sample. This tedious procedure was replaced by one using gradient formation by pump, eliminating pH neutralization of the monomer mixture, substituting polymerization at 50 °C for one at the temperature of electrophoresis (10 °C in this study) and omitting washing and drying of the gel prior to use. Carrier ampholyte (CA) containing IPG gels were formed in the same way except that CAs were added to the polymerization mixture. Pre-electrophoresis of IPG gels, formed by either the conventional or the simplified procedure, was found to be detrimental to the IPG patterns of proteins. The simplified procedure also allowed one to conduct IPG electrophoresis in gel tubes, eliminating lateral zone diffusion.
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  • 21
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    Weinheim : Wiley-Blackwell
    Electrophoresis 7 (1986), S. 401-406 
    ISSN: 0173-0835
    Keywords: Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Brief alkali treatment of nitocellulose-bound protein markedly enhanced subsequent staining of protein with India ink or colloidal gold but not Amido Black. Following alkali treatment, India ink staining approaches colloidal gold staining in sensitivity and exceeds the latter method in clarity and economy. Furthermore, apparent protein-to-protein variation is reduced, allowing the method to be used for sensitive staining of protein transfers. Simple, high sensitivity staining of nitrocellulose-bound protein using India ink can be achieved after alkali treatment in less than 2 hours.
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  • 22
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    Electrophoresis 7 (1986), S. 407-413 
    ISSN: 0173-0835
    Keywords: Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Highly acidic proteins are difficult to study using conventional electrofocusing and electrophoretic techniques. For example, the lysosomal enzymes from the cellular slime mold Dictyostelium discoideum have isoelectric points (pI) around 3-4 due to extensive phosphorylation and sulfation. To assess differences in anionic modifications among these lysosomal enzymes, we required methods that resolved acidic proteins on the basis of their net charge. The separation procedures needed to be rapid and convenient, allowing parallel analysis of a large number of samples. Using these criteria, we developed two methods, isoelectric focusing in horizontal agarose gels and native electrophoresis in vertical polyacrylamide gels, which are more useful than other available techniques. Since the mechanism by which each system separates proteins is different, both methods give important information about acidic proteins.
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  • 23
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    Electrophoresis 7 (1986), S. 413-416 
    ISSN: 0173-0835
    Keywords: Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Purified human blood clotting factor IX, although homogeneous by sodium dodecyl sulfate-polyacrylamide gel electrophoresis, showed two peaks when analyzed by crossed immunoelectrophoresis in the presence of calcium. Differential affinity of lectin from wheat germ (WGA) for the two forms of factor IX, detected by crossed affino-immunoelectrophoresis, demonstrated that carbohydrate moieties are involved in factor IX heterogeneities. The slow migrating peak has a higher affinity for WGA (Kd= 5.26 × 10-7 M) than the fast migrating peak (Kd= 1.29 × 10-5 M). This study emphasizes the usefulness of lectins as tools to assess homogeneity and integrity of glycoproteins.
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  • 24
    ISSN: 0173-0835
    Keywords: Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Isoelectric focusing in mixed carrier ampholyte-immobilized pH gradients (CA-IPG) is an effective way to separate proteins by charge. A method to prepare CA-IPG in capillary tubes and the description of the equipment used are outlined. Two-dimensional gel electrophoresis patterns of human serum and liver biopsies, with isoelectric focusing and CA-IPG as the first dimension, are presented. The comparison with two-dimensional gel electrophoresis patterns obtained by conventional carrier ampholyte pH gradient separation shows the excellent resolution and potential of this technique.
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  • 25
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    Electrophoresis 7 (1986), S. 492-495 
    ISSN: 0173-0835
    Keywords: Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: A new method for the apolipoprotein E (apo E) phenotyping directly from human serum has been developed. The method is based on isoelectric focusing of delipidated serum in vertical slab gel systems followed by blotting and immunostaining using polyclonal anti-apo E antibodies as the first antibody. Apo E phenotyping with this method in 150 serum samples gave exactly the same results as obtained with the conventional method based on isoelectric focusing of delipidated very low density lipoproteins isolated by ultracentrifugation and detected by protein staining. Compared with the conventional method, the present method is less expensive, suitable for large-scale screening purposes e. g. diagnosis of type III hyperlipidemia and needs only a few microliters of serum. By application for screening of hyperlipidemic sera, we were able to detect two patients with an apo E-1 variant and two others with “new” E-3 and E-4 mutants by the described methods. In addition apparent molecular weight variants of apo E could be detected by sodium dodecyl sulfate-gel electrophoresis of sera followed by blotting and immunostaining.
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  • 26
    ISSN: 0173-0835
    Keywords: Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Ultrathin-layer sodium dodecyl sulfate-polyacrylamide gradient gel electrophoresis in combination with silver staining is a highly sensitive and rapid method for molecular size analysis of urinary proteins. First results are achieved after 4 h (electrophoretic run, 100 min, followed by Coomassie Brilliant Blue staining, 2 h). After additional silver staining, including a recycling step, the results are ready for evaluation within 7 h. Urine samples do not need to be concentrated. Within a single gel, 25-27 samples can be run side by side under identical conditions and thus compared without ambiguity. By coelectrophoresis of pure proteins and immunological analysis 13 urinary proteins could be identified and for 7 of them the detection limits were determined. Glomerular protein patterns in samples of urine with a protein concentration in the normal range are compared with the concentration of albumin and transferrin measured by a sensitive enzyme immunoassay. Typical renal and extrarenal protein patterns are shown.
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  • 27
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    Electrophoresis 7 (1986), S. 524-526 
    ISSN: 0173-0835
    Keywords: Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Hair proteins have been successfully analysed by high resolution two-dimensional electrophoresis by avoiding S-carboxymethylation which has previously dictated the use of alternative two-dimensional procedures. The high and low-sulfur proteins are simultaneously resolved within the pI range 3-9 and their electrophoretically determined Mr values are consistent with molecular weights obtained by physical methods.
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  • 28
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    Electrophoresis 7 (1986), S. 518-523 
    ISSN: 0173-0835
    Keywords: Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Water soluble allergens of grass pollen (Dactylis glomerata) were purified by two successive steps of preparative isoelectric focusing in a flat bed of granulated gel and controlled by analytical isoelectric focusing in agarose gels. In order to separate components cofocusing in the same pH zone but having different electrophoretic mobilities, preparative zone electrophoresis in granulated gels was performed. The homogeneity of the fractions recovered was tested by isoelectric focusing and zone electrophoresis, followed by radioimmunodetection of the allergenic molecules on nitrocellulose prints. The major allergen of Dactylis glomerata pollen was purified with a yield of 7.5 mg from 10 g of pollen grains.
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  • 29
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    Electrophoresis 7 (1986), S. 527-529 
    ISSN: 0173-0835
    Keywords: Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: The degradation kinetics of Immobiline pK 9.3 (0.2 m in H2O) have been studied over a period of 2-years in the frozen state. The apparent hydrolysis rate (derived from the shift of myosin spots in a two-dimensional map) is 20% per year (or 10% if incorporation of acrylic acid, an hydrolysis product, is accounted for). Such reactions in frozen solutions are not uncommon (cf. the spontaneous mutarotation of glucose, Kiovsky, T. E. and Pincock, R. E., J. Amer. Chem. Soc. 1966, 88, 4704-4710).
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  • 30
    ISSN: 0173-0835
    Keywords: Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Progesterone therapy of androgenized rats results in the elimination of histological abnormalities of the uterus associated with constant unopposed oestrogenic stimulation. Subcellular fractions prepared from uteri of normal, androgenized and progesterone treated animals have been analysed by two-dimensional gel electrophoresis. In all fractions, protein changes were observed as a result of androgenization and subsequent progesterone therapy. The identity of some of these proteins has been assigned following peptide mapping. Following progesterone therapy, the relative proportion of cytosolic tubulins, tropomyosins and D-glucose-6-phosphate dehydrogenase were increased. In the abnormal uterus, a protein with similarity to the B subunit of creatine kinase was present in the mitochondrial fraction but could not be detected in the cytosol. Subsequent to progesterone therapy, this protein was no longer detectable in the mitochondrial fraction whilst two molecular forms of the B subunit of creatine kinase appeared in the cytosol. These hormonally-sensitive changes in both structural and enzymatic proteins, which are ubiquitous to most cell types, are discussed in relation to morphological differentiation of the uterus and the molecular mechanisms underlying cell growth.
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  • 31
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    Electrophoresis 7 (1986), S. 536-536 
    ISSN: 0173-0835
    Keywords: Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
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  • 32
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    Electrophoresis 7 (1986) 
    ISSN: 0173-0835
    Keywords: Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology
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  • 33
    ISSN: 0173-0835
    Keywords: Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: The human plasma transthyretin (TTR, prealbumin) variant TTR(Met30) has been separated from normal TTR(Val30) by double one-dimensional electrophoresis using polyacrylamide gel electrophoresis followed by hybrid isoelectric focusing. The procedure appears to be appropriate for identification by the screening of patients with familial amyloidotic polyneuropathy of Portuguese type I. This is the second example to support the recently expressed hypothesis (Altland et al., Electrophoresis 1986, 7, 251-259) that substitutions of electrically neutral amino acids (e. g. methionine for valine at position 30) in a polypeptide chain (e. g. the TTR monomer) may be detected by isoelectric focusing under denaturing conditions (e. g. hybrid isoelectric focusing in the presence of 8 M urea, 50 mM dithiothreitol) when the exchange is close to a charged amino acid (e. g. histidine at position 31, pI (TTR) = 5.7, pKa (His) = 6.0).
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  • 34
    ISSN: 0173-0835
    Keywords: Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: A demountable polyacrylamide gel system is described that uses commercial components and can be adapted to any slab system. The use of GeldBond PAG film produces polyacrylamide gels that can be easily handled and allows separation of the conditions needed for polymerization from those for electrophoresis. Polymerization is performed with one common protocol, and the gel is disassembled. Gels can then be soaked or stored in any desired solutions, followed by reassembly of the equilibrated gel and electrophoresis. This procedure allows for a wide range of electrophoretic conditions starting with a single type of polymerized gel as well as permitting use of systems that have technical difficulties under normal cirumstances such as horizontal gels or those containing the cationic detergent, cetyltrimethylammonium bromide.
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  • 35
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    Keywords: Chemistry ; Biochemistry and Biotechnology
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    Notes: Two-dimensional electrophoresis with isoelectric focusing in immobilized pH gradients in the first dimension was applied to the fractionation of hydrophobic proteins from the plasma membrane of a Streptococcus strain. The detergents incorporated into the first-dimensional gel slab, especially the zwitterionic ones of the sulfobetaine series, interfere with protein transfer from the first to second dimension by formation of mixed micelles with sodium dodecyl sulfate molecules. In order to reduce their concentration an elution protocol was devised including: (i) fixation for 1 h in 50 % methanol - 12 % acetic acid; (ii) washing with distilled water for 30 min; (iii) equilibration in concentrated Tris buffer; (iv) denaturation in 5 % sodium dodecyl sulfate - 2 % 2-mercaptoethanol. When counting the number of resolved spots in the protein patterns after two-dimensional electrophoresis, the relative solubilizing efficiency of different detergents scored as follows: Nonidet P-40 (NP-40) 〉 (3-[3-cholamidopropyl)dimethylammonio]-1-propananesulfonate (CHAPS) 〉 N-dodecyl-N, N-dimethylammonio-3-propanesulfonate (sulfobetaine SB 12).
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  • 36
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    Electrophoresis 7 (1986), S. 544-551 
    ISSN: 0173-0835
    Keywords: Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Proteins separated by isoelectric focusing of 20 samples and polyacrylamide gel electrophoresis of 10 samples in the same batch were stained with silver and were scanned with a computerized laser beam densitometer to obtain integrations values. A linear relationship was found between densitometric integration values (staining intensities) of proteins and their loads up to 600 ng (actin, carbonic anhydrase) or 1000 ng (albumin, creatine kinase), respectively. The same amount (250 ng) of applied albumin, actin, carbonic anhydrase and creatine kinase resulted in differences in staining intensities of these proteins; staining intensities of albumin and creatine kinase were similar, however: both were 1.8 X higher than the staining intensity of carbonic anhydrase and 2.3 X higher than of actin. Six human aortic intima proteins (ML-1, ML-2, P27, -14, P27,-18, P27,-19.5, P110) were selected for quantitative studies of the relationship between loads of intimal extract and the integration values of these proteins. Linear responses were found for these proteins in loads from 5 μL to 20 μL of intimal extract, corresponding approximately from 15 μg to 60 μg of total proteins applied to the focusing gel. When carbonic anhydrase was included with each sample, as an internal absorbance calibrator, we could express integration values of other proteins in relative amount in ng of carbonic anhydrase and thus compensate for variation in fixation, developing and staining conditions from batch to batch.
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  • 37
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    Electrophoresis 7 (1986), S. 552-557 
    ISSN: 0173-0835
    Keywords: Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: A computer-controlled version of recycling isoelectric focusing has been applied to the purification of recombinant human leukocyte interferons (IFNs) from E. coli. The system is based on continuous recycling between a 12-channel heat-exchange reservoir and a 12-channel focusing cell. It contains ten pH meters with probes in each of the flowing channels and two ultraviolet spectrophotometers with five flow cells per instrument. A minicomputer system acquires real-time data of pH and optical density measurements, controls and continuously monitors voltage and power outputs across the focusing cell, and generates on-line multi-color graphics on an x-y plotter. Recycling isoelectric focusing in the presence of 4 M urea resulted in removal of contaminating bacterial pyrogens from recombinant IFN alpha-2 with complete retention of specific antiviral activity. It also produced a 25-fold purification of crude recombinant IFN alpha-5 in a single step and resolved two biologically active species. These data suggest that recycling isoelectric focusing may be incorporated into the design of simple schemes for the purification of a variety of recombinant proteins.
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  • 38
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    Topics: Biology , Chemistry and Pharmacology
    Notes: Ampholine pH 4-6 and Pharmalyte pH 4.2-4.9, 4.5-5.4 or 5-6 have been used to improve the resolution of the simplified technique of high resolution two-dimensional electrophoresis. All give excellent resolution but Pharmalyte interferes with protein detection methods to an extent which increases with the pH range of the mixture. The effect is characterised by a progressive increase in the intensity and area of background stain associated with the anode and cathode regions of the two-dimensional gels. It is minimal following Serva Blue R (Coomassie Blue) staining but severe following silver staining.
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  • 39
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    Electrophoresis 7 (1986), S. 575-576 
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    Keywords: Chemistry ; Biochemistry and Biotechnology
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  • 40
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    Electrophoresis 7 (1986), S. 570-572 
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    Keywords: Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Direct gene analysis of the haptogobin (Hp) polymorphism was carried out by Southern blotting using an Hp cDNA probe. Two types of polymorphism were observed: the first, after EcoRI, HindIII and PstI digestion, is due to an intragenic duplication and corresponds to the Hp-α protein polymorphism; the second type, due to point mutation, was represented by two additional restriction sites for EcoRI and PstI. The univocal correspondence between the first type fragment length variants and protein polymorphism of the duplication type permits the establishment of the genotype at the DNA level, and mutational variants of the second type add new markers; the method described here also permits detection of the real genotype of Hp0 alleles.
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  • 41
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    Electrophoresis 7 (1986), S. 577-577 
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    Keywords: Chemistry ; Biochemistry and Biotechnology
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  • 42
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    Electrophoresis 7 (1986), S. 1-18 
    ISSN: 0173-0835
    Keywords: Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology
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  • 43
    ISSN: 0173-0835
    Keywords: Chemistry ; Biochemistry and Biotechnology
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    Topics: Biology , Chemistry and Pharmacology
    Notes: A new approach to isoelectric focusing in polyacrylamide gels is described, based on the use of rehydratable gels which in dry form could be stored for extended periods and which prior to use were rehydrated with solutions of any composition. Ultrathin 60-240 μm polyacrylamide gels, with different composition (5 % T, 3 % C; 3 % T, 4 % C; 3 % T, 20 % C), were polymerized under well-standardized conditions and, after polymerization, washed exhaustively with distilled water to remove any unreacted monomers, catalysts or soluble polymers. The washed gels were impregnated with suitable additives, before drying, to preserve gel functionality on storage. Polyol compounds, such as glycerol, sorbitol and dextran, as well as synthetic polymers like polyethylene glycol and polyvinylpyrrolidone, were the most efficient additives when incorporated into the gel in a concentration of 1-10 %, either as single substances or in different combinations. Prior to isoelectric focusing the dry gels were rehydrated to the original gel volume with a solution of carrier ampholytes, in some experiments with added separators or urea. Kinetic studies have shown rehydration, depending on gel thickness, to be complete within a few minutes. Isoelectric focusing in rehydratable gels was consistently more reproducible than in wet gels by such criteria as regularity of patterns and coalescence of marker proteins, including ferritin, applied at different positions. Rehydratable gels tolerated higher field strengths at the final stage of isoelectric focusing, with typical values of 500-900 V/cm and thus, at a given volt X hour product, equilibrium focusing could be attained in a shorter time, with improved resolution and sharper zones. Ultrathin-layer isoelectric focusing in rehydratable gels proved insensitive to high salt concentrations (up to 0.5 M) of the samples. Rehydratable gels represent a new generation of gels, excelling over the traditional wet gels by better standardized properties, convenient handling and unsurpassed flexibility.
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  • 44
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    Topics: Biology , Chemistry and Pharmacology
    Notes: This report describes a method of in vitro labelling of proteins designed for subsequent analysis of the sample by two-dimensional electrophoresis. As much as 106 cpm can be incorporated in 5 μg of proteins. As the reagent reacts with the amino groups, virtually all the proteins are labelled. Thus, this method is far more sensitive than silver staining and may prove useful when extremely low amounts of sample are to be analysed.
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  • 45
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    Electrophoresis 7 (1986), S. 58-58 
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  • 46
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    Electrophoresis 7 (1986), S. 72-75 
    ISSN: 0173-0835
    Keywords: Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: We have prepared a standard of human myoglobin by flat bed isoelectric focusing, to be used in immunological and chemical methods of measurement in clinical biology. Myoglobin was extracted from human psoas or myocardium and then purified by preparative isoelectric focusing in a granulated gel. The purified myoglobin was examined by analytical isoelectric focusing, high performance liquid chromatography (HPLC), immunoelectrophoresis, and two-dimensional gel electrophoresis. Myoglobin was quantified by three methods: (i) Drabkin's method, and by the determination of iron using (ii) the bathophenanthroline method, and (iii) the atomic emission method. There was good correlation between all three methods. Purified myoglobin was stabilized by conversion to the cyanmetmyglobin form, and stored until use at 4 °C (± 2 °C). or at - 20 °C in the liquid state after addition of ethylene glycol.
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  • 47
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    Notes: The reproducibility of protein migration was studied in three electrophoretic systems: sodium dodecyl-sulfate electrophoresis on polyacrylamide gradient, isoelectric focusing on immobilized pH gradients and two-dimensional charge-size separations. The gradient gels were poured either with a two-vessel apparatus or with a set of computer-driven burettes, as described by Altland and Altland (Electrophoresis 1984, 5, 143-147). Standard deviation on band position was cut by 20-50% with the latter approach in comparison with the former. Typical results were: sodium dodecyl sulfate-polyacrylamide gel electrophoresis, 0.6 mm (over a total length of 135 mm); immobilized pH gradients, 0.6 mm (for 179 mm length); two-dimensional separations, 0.8 mm (χ-axis), 0.6 mm (y-axis).
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  • 48
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    Notes: Two-dimensional electrophoresis and sodium dodecyl sulfate-polyacrylamide gel electrophoresis, followed by silver staining or specific immunoblotting analysis, was applied to the characterization of gamma-glutamyltransferase (GGT, EC 2.3.2.2.) in rat tissues. We confirmed that purified kidney GGT is a dimer composed of two non-identical subunits with molecular masses of about 50 and 30 kDa. Both the light and the heavy subunits were separated into 6 and 2 protein bands, respectively. Antibody fractions against the 30 and 50 kDa subunits, purified by immunoaffinity from a whole antiserum directed to the rat kidney enzyme, recognized their corresponding subunits and did not cross-react with each other. Studies of the reactivity of these antibodies towards GGTs from kidney and liver homogenates revealed an intraspecies dissimilarity in the molecular architecture of the kidney and liver GGTs, especially concerning the 30 kDa subunit. Following phenobarbital treatment of animals we observed an increase in immunoreactive GGT, accompanied by the appearance of additional polypeptides with more basic isoelectric points and higher molecular mass.
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  • 49
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    Electrophoresis 7 (1986), S. 99-99 
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    Keywords: Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: A common problem, when using Silane A 174 to bind polyacrylamide gels to supporting glass plates, is that the gel also binds to the cover glass in the gel casting frame. This can be avoided by using a low concentration of Silane A 174 and by rinsing the supporting glass plate with acetone after the Silane A 174 treatment.
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    Electrophoresis 7 (1986), S. 56-57 
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    Keywords: Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Lateral streaking or bending in vertical one-dimensional slab gel electrophoresis can be completely avoided if a comb-gel made up in electrophoresis buffer is placed on top of the stacking gel or sample gel.
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  • 51
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    Electrophoresis 7 (1986), S. 106-106 
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    Keywords: Chemistry ; Biochemistry and Biotechnology
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  • 52
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    Electrophoresis 7 (1986) 
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  • 53
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    Electrophoresis 7 (1986), S. 100-103 
    ISSN: 0173-0835
    Keywords: Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: A method is described for direct analysis of the reaction mixtures of the production of the herbicide glyphosate and the growth regulator glyphosine by capillary isotachophoresis providing simultaneous determination of the products N-phosphonomethyl-glycine and N.N-bis(phosphonomethyl)glycine as well as of all important reaction components - sulfuric, formic, phosphorous, phosphoric, hydroxyacetic, nitrilotriacetic, iminodiacetic and N-phosphonomethyliminodiacetic acids and glycine. The method is suitable for the analyses both of the final products and of mother liquors, where the maximum ratio of the concentrations ranges within 1:100. The time of analysis is dependent on the sample composition and ranges within 5-20 min. relative standard deviation of a single determination being less than 4 rel. %.
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    Electrophoresis 7 (1986), S. 121-128 
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    Keywords: Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: A mathematical approach to the behavior of isotachophoretic and counter ion components in the steady state of isotachophoresis of weak acids was developed. In steady state, the partial time derivative can be replaced by the -ν times χ derivative, where ν is the velocity of isotachophoresis. Application of this relation to mass balance equations of the components gave the expression of concentration gradients as functions of concentrations of the components, conductance and the H+ ion concentration gradient. The results were inserted into the χ derivative of the electric neutrality equation and the electric current equation, including both electrophoretic and diffusional currents. These equations were solved for conductance and H+ ion concentration gradients and the latter quantities could be expressed as functions of concentrations of the components. Thus, concentration gradients of the components were calculable from the concentrations. Given proper initial or boundary conditions for the concentrations of the components, numerical integration gave pH, conductance and concentration profiles of the components. The results were in agreement with those of capillary isotachophoresis experiments.
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  • 55
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    Electrophoresis 7 (1986), S. 128-133 
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    Keywords: Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: The 21 free amino acids commonly encountered in proteins have been transformed into “carrier ampholyte” species by reacting their primary amino groups with dansyl chloride. These derivatives can thus be focused in an immobilized pH gradient covering the pH 3.1 to 4.1 interval, except for arginine, which still retains a pI of 8.8. Due to their inherent fluorescence, the dansyl derivatives are revealed in UV light, with a sensitivity of the order of 2-4 ng/mm2. All nearest neighbors are separated except for the following couples: Asn-Gln, Gly-Thr, Val-Ile and Cys-Cys2, with a resolving power, in a ΔpI scale, of the order of 0.0018 pH units. Except for a few cases (notably the aromatic amino acids) the order of pI values is well correlated with the pK values of carboxyl groups, suggesting that the latter are not altered by dansylation. From the set of pKCOOH -pI values of the different amino acids, the pK of the tertiary amino group in the dansyl label has been calculated to be 5.11 ± 0.06. Knowing the pK of the amino-dansyl and the pI of the excess, free dansyl label (pI = 3.34) we have derived, for its sulfonic acid group, a pK of 1.57.
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  • 56
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    Notes: Comparison between highly repeated DNA fragments of eucaryotic DNA digested by restriction endonucleases and the corresponding pattern of a completely digested DNA can be used as a criterium of complete digestion before the Southern blotting procedure. Results are presented for highly repeated fragments of human DNA, partially and completely restricted by six different endonucleases. Direct visualization of these fragments was obtained by ethidium bromide staining after agarose gel electrophoresis. Fragments corresponding to a complete DNA digestion were retained and can be used as reference.
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    Electrophoresis 7 (1986) 
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    Electrophoresis 7 (1986), S. 150-151 
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    Topics: Biology , Chemistry and Pharmacology
    Notes: The pK values of the chemical processes which take place in Tris-borate buffers are determined with higher accuracy using more precise Tris ion and boric acid pK values, and the buffer capacities at different pH values are calculated. The results confirm that Tris-borate buffers contain a complex compound with betainic structure previously described as “Tris-boric” acid.
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    Electrophoresis 7 (1986), S. 152-152 
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    Electrophoresis 7 (1986), S. 166-171 
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    Keywords: Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: A novel highly sensitive method for the detection and quantification of proteinase activity is presented. The proteinases were forced electrophoretically into the substrate (sodium caseinate) containing agarose gel. The formation of enzyme-substrate complexes retarded the migration of the proteinases in the electric field and decreased the overall mobility of the enzymes. The proteinases were released as a result of the degradation of the substrate, and consequently the height of the obtained rocket shaped zones of hydrolysis were proportional to the concentration of proteinases in the samples. The electrophoretic method accelerated penetration of the substrate-containing gel by the proteinases and subsequently resulted in a 100-fold increase in sensitivity as compared to the radial diffusion method, depending entirely on diffusion.
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  • 61
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    Notes: Previous studies by chromatography and electrophoresis have demonstrated that myosin is composed of two classes of polypeptide chains: high relative molecular mass (Mr) components (200 000) and a class of lower Mr species, called the “light chains” (LC). It has been shown before by others that the slow-twitching fibers contain 2 types of isoforms: LC1s and LC2s, while the fast-twitching fibers contain 3 types: LC1f, LC3f and LC2f, the latter also existing as phosphorylated forms. In the present investigation, utilizing two-dimensional (2-D) maps generated with narrow immobilized pH gradients in the first dimension, a higher resolution of the myosin LC has been achieved. The LC1s chains are further fractionated into at least four isoforms; LC2s into three; LC2f into four and LC3f into three sub-species in rabbit muscles. Skeletal muscle tropomyosin, which is separated into three forms (αs, αf and β), is here resolved into six components, while actin from skeletal muscle, previously described mainly as a single chain (α), is here sub-fracionated into four isoforms of identical Mr and different charge. The series of isoforms here reported could represent a fine probe for investigating such complex phenomena as the cellular differentiation of human satellite cells from normal and pathological subjects in greater detail than before.
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  • 62
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    Notes: A novel ionophoretic technique for the study of complexes especially mixed ones has been described in the communications from this laboratory. Here with the help of this technique the stability constants of the complexes M-nitrilotriacetate-threoninates have been found to be 5.24, 5.01, 3.54 and 3.21, respectively.
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    Electrophoresis 7 (1986), S. 239-239 
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    Electrophoresis 7 (1986), S. 239-239 
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  • 65
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    Notes: A program in BASIC Microsoft for a microcomputer is described for the analysis of electrophoretic patterns obtained by polyacrylamide gel electrophoresis. The program enables a rapid calculation of relative molecular masses and designs three types of graphs: the protein pattern, the linear representation of molecular masses and the linear regression curve calculated from several standard proteins. The application of this program for the study of serotypes A and B of the yeast Candida albicans is shown.
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  • 66
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    Notes: Development of techniques for silver staining of proteins separated by polyacrylamide gel electrophoresis has increased experimental detection limits. However, the precise basis for the reaction between silver and polypeptides is still unclear and, depending upon the choice of silver reagent, may even differ. We compared protein stain intensity with silver diamine (ammoniacal silver) and silver nitrate reagents based on amino acid composition by determining the protein amount required to generate an arbitrary staining intensity and then calculating moles of each amino acid present in some representative proteins. We compared these values for each amino acid, taken singly, as well as for combinations of two and more. In no case could staining be attributed entirely to specific or classes of amino acids, thus supporting the argument that an inherent difference exists between primary reactive centers for the two staining reagents.
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  • 67
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    Notes: Human parotid saliva proteins fractionated by preparative isoelectric focusing into 3 main fractions have been characterised electrophoretically and immunochemically. The anodic proteins constitute a polymorphic family of collagenase and trypsin sensitive, immunochemically related, phosphoproteins. Many of these contain a common polypeptide of Mr 23 000 either alone or in combination with other lower (Mr 21 000) or higher (Mr 25 000) molecular weight polypeptides. Parotid amylase was substantially purified by this technique and an antiserum against these fractions reacted monospecifically with amylase in a number of systems. The cathodic proteins are all collagenase sensitive proteins with Mr values of 12 500 to 77 000.
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    Electrophoresis 7 (1986), S. 339-341 
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    Keywords: Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Pea protoplast dielectrophoretic coefficients were measured in AC fields of different frequencies applied between concentric cylindrical metal electrodes, outer and inner radii, 0.24 mm and 1 mm, respectively. The values for 0.5 M mannitol solutions are: (6.0, 1.0, 5.6, 16.0 and 17.8) X 10-24Fm2 at frequencies 0.05, 0.1, 0.6, 1 and 8 MHz, respectively. The specific polarizabilities (dielectrophoretic coefficients per unit volume of the protoplasts) are: (5.0, 0.7, 4.0, 12.0 and 13.0) X 10-10Fm-1, respectively. Below 10 kHz dielectrophoretic effects were not observed. Cell rotation was observed in the frequency range from 1 kHz to 10 kHz. These results may be of use in cell separation and electrofusion in scientific research and technology.
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  • 69
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    Electrophoresis 7 (1986), S. 345-345 
    ISSN: 0173-0835
    Keywords: Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology
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  • 70
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    Electrophoresis 7 (1986), S. 342-344 
    ISSN: 0173-0835
    Keywords: Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Proteins with molecular weight between 66 000 and 950 000 were subjected to electrophoresis in 3 to 30 % linear gradients of polyacrylamide with volt-hour products between 2000 and 20 000. From the experimental data it was concluded that displacement of proteins decreased proportionally to the logarithm of time of electrophoresis. With these coordinates the fitness of the curves was found to be excellent (correlation coefficients were better than 0.993 for the analyzed proteins). These results support the hypothesis that there is no limit to be reached by a protein during its migration in a linear gradient of polyacrylamide. In addition we observed that the rate of decrease in mobility was proportional to the size of the protein.
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  • 71
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    Electrophoresis 7 (1986), S. 89-95 
    ISSN: 0173-0835
    Keywords: Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: With the aid of two-dimensional electrophoresis, the immunoglobulins (Ig) in cerebrospinal fluid (CSF) were separated into heavy and light chains and visualized with silver staining. CSF from 36 patients with no abnormal immunologic activity in the central nervous system show a constant pattern of light chain subfractions, however varying strongly in their respective quantities. In 40 patients with inflammatory diseases such as confirmed multiple sclerosis (MS) (n = 10), neurosyphilis (n = 6), lymphocytic meningoradiculitis (n = 3), novel immunoglobulins appear and form a so-called oligoclonal zone in the light chain region. By comparing various oligoclonal zones, differences were found between the arrangement of the novel Ig light chains and the polyclonal light chain background. In the region of the polyclonal light chain background certain protein fractions appear which are non-immunoglobulin and which are not found in serum. The protein fraction at the isoelectric point of 7.8 appears in 9 out of 10 confirmed MS cases, but in none of the 6 neurosyphilis and 3 lymphocytic miningoradicultis cases. In one case of neurosyphilis with an extremely high gamma-globulin content in CSF we found an oligoclonal zone in the heavy chain region.
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  • 72
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    Topics: Biology , Chemistry and Pharmacology
    Notes: Micro-polyacrylamide gel electrophoresis (micro-PAGE) has been shown to be useful for molecular size separation of urinary proteins. In addition to the sodium dodecyl sulfate micro-gradient gel electrophoresis in 10 μL capillaries, which is used routinely for examination of proteinuria in our laboratory, we tried micro-gradient slab gel electrophoresis (micro-slab-PAGE) for molecular weight determination of urinary proteins. It was also employed for monitoring patients with proteinuric diseases. For detailed studied of urinary proteins, micro-two-dimensional-electrophoresis is recommended.
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  • 73
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    Electrophoresis 7 (1986), S. 148-149 
    ISSN: 0173-0835
    Keywords: Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: A technique of isoelectric focusing of proteins from single pollen grains has been developed using ultrathin polyacrylamide gels. On a single gel, one hundred grains may be compared for total proteins or enzyme patterns. With this technique it was possible to reveal heterogeneity of pollen grains in a population at a genetic level and in relation to pollen viability.
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  • 74
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    Electrophoresis 7 (1986) 
    ISSN: 0173-0835
    Keywords: Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
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  • 75
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    Topics: Biology , Chemistry and Pharmacology
    Notes: Electrofocusing on diagonal immobilized pH gradients was designed to combine high field strength with a flat pH gradient over a wide pH range, circumventing the need for extremely high voltage in long, conventionally oriented focusing gels. The technique was found to be applicable at 500 V cm-1 to gels of 35 cm length of a flat pH gradient with a predicted pH range of 3.8 to 9.8, allowing for a focusing time of 2 h. Note that the equivalent flat pH gradient gel of 25 cm length at the same field strength would require application of 12 500 V. However, preliminary results indicate that the theoretically expected improvement in resolution due to high field strength does not materialize. This may be due to a distorted electric field caused by non-uniform conductance features inherent in the method and by the passage of the current through the isoelectric protein zones.
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  • 76
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    Topics: Biology , Chemistry and Pharmacology
    Notes: Affinity electrophoresis was applied to determine the dissociation constants and the thermodynamic parameters for the interactions between the mouse myeloma, MOPC 315, and trinitrophenyl (Tnp) and dinitrophenyl (Dnp) haptens. The myeloma protein consists of monomeric, dimeric, and trimeric forms of IgA. The dimer had a higher affinity to the haptens than the monomer, but its Fab' fragment had lower affinity than the monomer. All of these myeloma proteins had higher affinities to Tnp-hapten than to Dnp-hapten. The affinity of MOPC 315 proteins increased when the temperature increased. The van't Hoff plots for all of these interactions gave straight lines within the temperature range from 7 °C to 40 °C. The ΔH° were calculated by using the linear van't Hoff plots. The ΔS° were calculated from the D̊H° and D̊G°. The D̊H° and D̊S° were both positive. Hence, the interactions were endothermic and hydrophobic.
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  • 77
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    Topics: Biology , Chemistry and Pharmacology
    Notes: A method is described which allows the preparation of retinae, laminae, opticallobes, protocerebrum and proboscis of single heads of Drosophila. The protein content of these tissues was examined with sodium dodecyl sulfate-polyacrylamide gel electrophoresis followed by Coomassie Brilliant Blue R-250 and glycoprotein staining. A catalog of 39 major proteins or protein subunits was obtained. Their relative proportions were determined quantitatively for the different tissues from Drosophila wildtype strains AS and C-S as well as the mutant sevLY3.
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  • 78
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    Keywords: Chemistry ; Biochemistry and Biotechnology
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    Topics: Biology , Chemistry and Pharmacology
    Notes: Uncrosslinked polyacrylamide, a viscous liquid, provides a molecular sieving effect in electrophoresis qualitatively the same as that of crosslinked gels. This finding confirms previous results by others using uncrosslinked polyacrylamide mixed with various gel matrices. It provides a sieving medium constituted by an entirely and necessarily random association of inert fibers, as stipulated for interpretation of migration by the Ogston theory. Ferguson plots of several proteins in uncrosslinked polyacrylamide exhibit Yo values smaller and less divergent from one another than in 5 % crosslinked gels, suggesting a curvature of the Ferguson plots of crosslinked polyacrylamide gels at low %T. If linearity of these plots at low %T, 0 %C could be demonstrated, a means would be found to determine accurate values of free mobility by their linear extrapolation to 0 gel concentration. Potentially, uncrosslinked polyacrylamide at low concentrations may provide a tool for the analytical sieving of subcellular particles. However, electrophoresis in uncrosslinked polyacrylamide at concentrations of less than 10 % is perturbed by convection, and thus these potential applications will depend on combining it with a suitable anticonvective device.
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  • 79
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    Electrophoresis 7 (1986), S. 230-232 
    ISSN: 0173-0835
    Keywords: Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Recently we described a procedure for pouring immobilized pH gradients at ambient temperature in the presence of a neutral buffer (0.1 M Tris-phosphate pH 6.8) (Altland and Rossmann, Electrophoresis 1985, 6, 314-325). After washing in plain water and in 1 % glycerolin water, the gels were dried, sealed in polyethylene bags and stored at -20°C until use. The reproducibility of a batch of 20 gels with a linear pH 6-10 gradient, poured under computer control, was studied by rehydrating the dried gels in a solution containing 8 M urea, 50 mM dithiothreitol and 0.5 % carrier ampholytes (pH 6-10) and by running human red cell lysates as samples. A comparison of the globin patterns obtained at various time intervals within a range of 7 months revealed that there was no detectable shift in the pH gradient within this period and that gels stored for 7 months can be used to clearly identify all human globins from newborns and adults. Since the tested pH gradient was prepared from Immobilines claimed as being the most sensitive to degradation by hydrolysis (e. g. Immobiline pKa 8.5 and 9.3), it is concluded that storage of dry gels, rehydrated prior to use, is a realistic alternative to the preparation of fresh gels from stored stock solutions for achieving reproducible results in long-term comparative studies.
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  • 80
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    Notes: A research method is described for producing ultramicrogradient acrylamide gels in 0.5 μL constant volume capillary tubes (inner diameter 130 μm and 32 mm length) suitable for the determination of protein in kidney tubule fluid. Previous methods have been limited to gels contained in 1 and 5 μL capillary tubes. The acrylamide gel concentration varies from 4 to 27% in a functional gel of approximately 40 nL and a length of 2.0 to 2.9 mm. Relative migration distances in these gels of known proteins of varying molecular weight (6000 to 669 000) are comparable to those measured in gels contained in 5.0 μL capillary tubes. After electrophoresis, the gels are extruded from the capillary tubes, stained with Fast Green, destained and scanned in a Joyce-Loebl microdensitometer with integrator unit. Such gels are capable of retaining and quantitating low molecular weight proteins contained in nanoliter volumes of biological fluids. The reproducibility of this technique for 0.5 μL capillary gels is comparable to that achieved with the routine analysis of proteins in unconcentrated urine using 5.0 μL gels. Examples are given of protein analyses in kidney tubule fluids and urine obtained from normal rats and those with glomerulonephritis.
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  • 81
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    Electrophoresis 7 (1986), S. 221-226 
    ISSN: 0173-0835
    Keywords: Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: A compact device, capable of being clipped onto the end of a 3 mm thick analytical polyacrylamide slab gel, has been developed for the collection of resolved protein zones as they elute from the end of the gel. Its unique feature is that eluted proteins were collected between two polyacrylamide-embedded paper membranes and removed either by continuous or intermittent buffer elution. Because of this direct coupling to large gels identical to those used for analytical electrophoresis, protein zones were obtained with high resolution. The method was applicable to non-denaturing cathodic and anodic electrophoresis, as well as sodium dodecyl sulfate electrophoresis. Medium-scale quantities (up to 10 mg/cm2 cross-sectional area) of protein were fractionated in as little as 4 h with high recoveries.
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  • 82
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    Electrophoresis 7 (1986), S. 226-229 
    ISSN: 0173-0835
    Keywords: Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: When screening natural populations for genetic variation in mitochondrial (mt) DNA it is necessary to screen as many individuals as possible for as large a number of base pairs as possible. This report describes a combination of laboratory techniques - isolation of mtDNA by either density ultracentrifugation or a phenol extraction procedure and DNA fragment visualization by a sensitive silver staining technique. These routines remove the major restriction of tissue sample size and number of individuals that can be screened and allows the investigation of at least 1000 base pairs from 1 g of tissue or 3-400 base pairs from 100 mg of frozen tissue.
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  • 83
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    Electrophoresis 7 (1986), S. 232-235 
    ISSN: 0173-0835
    Keywords: Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Renouncing protein fixation with aldehydes, the polyacrylamide gels are incubated in alcoholic solutions of silver nitrate containing acetic acid at 60-70 °C. for a short time and developed with NaOH, also at 60-70 °C. Using various methods of protein fixation, the detection limits of human albumin were determined for 0.75 and 1.5 mm thick polyacrylamide gels with appropriate thickness correction. An overlay technique with silver nitrate containing polyacrylamide gels is described. Dispersing Coomassie Brilliant Blue G-250 in a solution containing HNO3 and NH4NO3 allows rapid silver staining of prestained gels.
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  • 84
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    Notes: Phenol extracted, alkali-treated lipopolysaccharide (aLPS) from vaccine strain (S19) Brucella abortus was demonstrated by two-dimensional gel electrophoresis to consist of at least ten silver staining, polydisperse analogues having different pIs. When tested on nitrocellulose immunoblots, all ten were antigenically reactive with bovine anti-B. abortus polyclonal sera, but only six reacted with anti-B. abortus O-antigen murine monoclonal antibody. Analogues focusing at different pIs were concluded to arise from differences in either core or O-antigen side chain structure or because of covalently bound protein. While not qualitatively different, aLPS from pathogenic B. abortus strain 2308 had lesser amounts of analogues 1, 2, 5, 6, and 8 than did aLPS from strain 19 (vaccine). The 2-D gel electrophoresis method was demonstrated to be of value in the analysis of aLPS from B. abortus and may be useful in the study of lipopolysaccharides from other sources.
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  • 85
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    Topics: Biology , Chemistry and Pharmacology
    Notes: Human genomic DNA probes labeled by nick translation with biotin 11-UTP were successfully used to identify single copy restriction fragment length polymorphisms following electrophoresis and Southern blotting onto nylon membranes. Two human probes found on chromosome 21 were used, each of which demonstrated polymorphisms using two separate restriction endonucleases. Compared to isotopic labeling of probes the biotin labels are safer, faster and more economical. The detection method of streptavidin-biotin-alkaline phosphatase permitted phenotyping in a matter of hours after hybridization of the probe to the human DNA fragments.
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  • 86
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    Electrophoresis 7 (1986) 
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    Keywords: Chemistry ; Biochemistry and Biotechnology
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  • 87
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    Electrophoresis 7 (1986), S. 293-293 
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    Keywords: Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
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  • 88
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    Electrophoresis 7 (1986), S. 291-292 
    ISSN: 0173-0835
    Keywords: Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: The electrophoretic behavior of esterase D (E.C. 3.1.1.1.) allozymes 1, 2 and 5 was studied in various buffers and pH ranges, and compared with results obtained on isoelectric focusing. It is shown that the relative mobility of ESD 2 and 5 allozymes is reversed according to the pH of the buffer system. In acidic pH ranges the mobility is: cathode 1〈2〈5 anode; using the same buffer system in basic pH ranges the following order is observed: 1〈5〈2. Technical improvements in agarose gel electrophoresis leading to a considerable economical advantage over the previously described methods are presented.
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    Electrophoresis 7 (1986), S. 295-296 
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    Electrophoresis 7 (1986), S. 297-303 
    ISSN: 0173-0835
    Keywords: Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Mathematical simulation of an isotachophoretic boundary between protein and weak acid was made on the assumption of steady state. In order to deal with a protein molecule, a Gaussian model for charge distribution of protein molecule was constructed, based on the assumption that acidic and basic residues on a protein molecule dissociate independently of each other. The results were roughly in agreement with protein stacking experiments with regard to boundary thickness and concentration of the stacked zone.
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  • 91
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    Notes: The changes in the migration of adenovirus type 2 structural proteins in sodium dodecyl sulfate polyacrylamide gels following various denaturation conditions or periods have been studied. Several factors such as proteolytic cleavages, disulfide bridges, carbamylation or residual charge effects which could lead to altered migration were screened. Resistant high order structures sensitive to the action of urea might cause these variations. A likely relationship between the difference of apparent molecular weight, frictional coefficient and hydrophobicity has been established.
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  • 92
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    Electrophoresis 7 (1986), S. 323-326 
    ISSN: 0173-0835
    Keywords: Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Superposed miniature agarose slab gels and relatively small plasmids were used to evaluate the DNA topoisomerase I activity associated with the chromatin of normal human fibroblasts at three different in vitro population doubling levels. Results obtained in a short period of time with a single miniature electrophoresis unit confirm an increase in DNA-relaxing enzyme activity with cell age.
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  • 93
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    Electrophoresis 7 (1986) 
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    Keywords: Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
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  • 94
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    Electrophoresis 7 (1986), S. 367-371 
    ISSN: 0173-0835
    Keywords: Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Mononuclear leukocytes of the human peripheral blood were separated by counter-current centrifugal elutriation. In this way a group of lymphocytes was isolated, which contained B-lymphocytes with an electrophoretic mobility (EM) of 0.9 × 10-4 (cm2 V-1 s-1) and T-lymphocytes with an EM of 1.1 × 10-4 (cm2 V-1 s-1). This group of lymphocytes was incubated for 7 days in the presence of monocytes and pokeweed mitogen. Then the culture supernatants were screened. Non-specific human antibodies were found in all culture supernatants. In 20% of the supernatants human antibodies against sheep red blood cells could be detected. The viable cells of the cultures were separated into 5 fractions by free flow electrophoresis. Then the cells of the different fractions were tested for their capability to produce antibodies. The tests revealed that antibody-secreting cells had an EM around 0.9 × 10-4 (cm2 V-1 s-1) and that the greater part of the cells, isolated from pokeweed mitogen cultures, had a significant higher EM. Thus free flow electrophoresis could be applied to enrich antibody-secreting cells ninefold.
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  • 95
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    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: In this series of papers, we describe the computer system we have developed for two-dimensional (2-D) gel analysis. Here the acquisition part of the system is described and a set of criteria able to measure the overall performance of the system is presented. These criteria are essentially based on frequency domain considerations using Fourier transforms. We show that the transfer function characteristics of the input system must be carefully checked to avoid any image distortion; we propose an easily computed criterion to obtain setting conditions giving a correct system response. These features are discussed considering the specificity of the 2-D gel images that can be well modeled by a multi-Gaussian surface. Then the visualization device and its main abilities to treat and modify the aspect of the images are presented. Statistical functions using second-order image histograms are introduced. They can be used to look at the general aspect of the images, as a global and accurate criterion for quality checking. For this purpose, covariance, entropy and inertia have been found to be most suitable. Second-order histograms give additional information on image anisotropy and can direct the user towards the convenient values of the parameters for the subsequent treatments. Coding is considered from both the point of view of image compression and image sending throughout a computer network. An efficient code protecting all the image informations is suggested and discussed.
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  • 96
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    Electrophoresis 7 (1986), S. 357-367 
    ISSN: 0173-0835
    Keywords: Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: This work describes the techniques used to detect the presence of a spot at a given place in a two-dimensional gel and to compute its volume. This is done using filtering techniques to extract significant information from rough images. Four types of treatments were applied to images in order to improve the detection of spots belonging to different categories. Mathematical techniques of morphology were used to lower the effect of spot overlapping, while histogram modifications using power functions were used to improve the detection of major and minor spots, respectively, thereby generating four processed images. On each generated image, spot detection is computed by looking at the local maxima. Then the four spots lists are gathered and the volume is computed according to a spot model. To improve the accuracy of volume detection, a spot model constituted by two half-Gaussian curves in each space direction is used. The pitch of each spot according to the horizontal direction is also computed. A total of 8 parameters, including spot position, shape parameters, surface intensity and volume, is gathered into a spot list which constitutes the reduced information which will be handled subsequently. The choice of a model allows us to get a round the improper volume calculations caused by spot overlapping. The mutual penetration of one spot into another is thus automatically taken into account. A set of statistical considerations is computed from these data in order to validate our spot model, to check for parameter independence, to obtain quality criteria which may be used to judge gel quality, to propose different diagnoses for the observed defaults and to lead to a self-adaption process of treatment parameters. These statistical considerations can be used to study the effect of each type of treatment and to compare the effects of each filter on the final result.
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  • 97
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    Keywords: Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Free flow electrophoresis was used for the purification of human tissue plasminogen activator (t-PA) produced by recombinant yeast cells. This method was employed for three principal reasons: (a) yeast t-PA purified by immunoaffinity chromatography was not pure enough to carry out protein chemical characterization, (b) the amount of yeast t-PA available for purification was extremely limited, (c) t-PA has a strong tendency to adsorb to support material; a support-free separation method therefore seemed to be a reasonable way to further purify the enzyme. Free flow electrophoresis was first performed using solutions containing the soluble proteins of yeast cell extract, and secondly, using t-PA fractions prepared by immunoaffinity chromatography, Yeast t-PA purified by immunoaffinity chromatography and then by free flow electrophoresis is more than 80% pure and suitable for characterization experiments such as glycosylation studies or N-terminal sequence determination.
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  • 98
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    Electrophoresis 7 (1986), S. 395-400 
    ISSN: 0173-0835
    Keywords: Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: A digital simulation of the behavior of amphoteric sample components in moving steady state boundaries is presented. Complete computer simulation data, including profiles of concentration, conductivity and pH as functions of time, are given for both cationic and anionic electrolyte configurations which incorporate one amphoteric sample constituent. The condensation of ampholytes in steady state moving boundaries is shown to proceed via an isotachophoretic mechanism and not by isoelectric focusing. Mobility (velocity) relationships necessary for sample components to form steady state zones are discussed.
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    Electrophoresis 7 (1986), S. 426-428 
    ISSN: 0173-0835
    Keywords: Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Murine Cu, Zn-superoxide dismutase (SOD) from erythrocytes has three isozymes, SOD-1A (pI 6.4), B (pI 5.7) and C (pI 5.0). It has been suggested that SOD-1A is formed epigenetically by asymmetric modification of SOD-1B where as SOD-1C is produced by treatment of superoxide dismutase with hydrogen peroxide. On two-dimensional gel electrophoretic analysis, each isozyme shows two forms, easily permuted into each other, and hence supposed to be in equilibrium. The zymogram patterns of murine liver, kidney, heart and brain are the same as those in erythrocytes although SOD activity levels are different in these tissues.
    Additional Material: 5 Ill.
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  • 100
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Electrophoresis 7 (1986), S. 429-430 
    ISSN: 0173-0835
    Keywords: Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: A simple and inexpensive system of a power supply for protein blotting is described. The blots are run using a 12 V car battery charger which is modified for laboratory use. Under these conditions even high molecular weight proteins of 300 000 can be completely transferred to the nitrocellulose paper in less than 5 h and efficiently immunostained.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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