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  • 1
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 41 (1995), S. 1602-1604 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Additional Material: 5 Ill.
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Macromolecular Rapid Communications 18 (1997), S. 921-925 
    ISSN: 1022-1336
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A series of 2,3-O-carboxymethylcelluloses (CMC's), which are regioselectively substituted at the C-2 and C-3 position, were prepared and their water solubility was examined. It was found that the lower limit for the degree of substitution (DS) value of water-soluble 2,3-O-CMC is about 0.3. This value was almost the same as that of CMC prepared in a slurry of isopropyl alcohol/water with isopropyl chloroacetate and sodium hydroxide, showing that the uniform alkylation is rather important to convert cellulose into water-soluble derivatives.
    Additional Material: 1 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    Chichester [u.a.] : Wiley-Blackwell
    Developmental Genetics 14 (1993), S. 339-346 
    ISSN: 0192-253X
    Keywords: ras ; CDC25 ; guanine nucleotide release factor ; signal transduction ; embryonic stem cell ; Life and Medical Sciences ; Genetics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
    Notes: A partial cDNA encoding a novel putative p2, ras guanine nucleotide release-inducing factor (GRF), GRF2, was amplified from murine embryonic stem cells. The presumptive catalytic region of GRF2 is related to the yeast Ras GRF encoded by CDC25. GRF2 is 80% identical to murine CDC25Mm/ras-GRF, but is more similar to yeast CDC25 than to other ras GRFs related to the Drosophila son of sevenless gene product. A 9-kb GRF2 messenger RNA was highly expressed in brain, but GRF2-specific antibodies recognized apparent GRF2 proteins in various mouse tissues in addition to brain. Thus GRF2 represents a novel widely-expressed protein that is highly related to CDC25Mm/ras-GRF, at least in its catalytic domain. Both GRF2 and CDC25Mm/ras-GRF are expressed in murine embryonic stem cells, suggesting that different Ras activators may regulate ras-dependent proliferation and differentiation in early mouse development. © 1993Wiley-Liss, Inc.
    Additional Material: 4 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Molecular Reproduction and Development 40 (1995), S. 338-344 
    ISSN: 1040-452X
    Keywords: Zygotes ; Cumulus-oocyte complexes ; Zona pellucida ; Gap junctions ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
    Notes: Several contemporary micromanipulation techniques, such as sperm microinjection, nuclear transfer, and gene transfer by pronuclear injection, require removal of cumulus cells from oocytes or zygotes at various stages. In humans, the cumulus cells are often removed after 15-18 hr of sperm-oocyte coincubation to assist the identification of the fertilization status. This study was designed to evaluate the function of cumulus cells during oocyte maturation, fertilization, and in vitro development in cattle. Cumulus cells were removed before and after maturation and after fertilization for 0,7,20, and 48 hr. The cumulus-free oocytes or embryos were cultured either alone or on cumulus cell monolayers prepared on the day of maturation culture. Percentages of oocyte maturation, fertilization, and development to cleavage, morula, and blastocyst stages and to expanding or hatched blastocysts were recorded for statistical analysis by categorical data modeling (CATMOD) procedures.Cumulus cells removed before maturation significantly reduced the rate of oocyte maturation (4-26% vs. 93-96%), fertilization (0-9% vs. 91-92%), and in vitro development at all stages evaluated. Cumulus cells removed immediately prior to in vitro fertilization (IVF) or 7 hr after IVF reduced the rates of fertilization (58-60% and 71%, respectively, vs. 91-92% for controls), cleavage development (40-47% and 53-54% vs. 74-78% for controls), and morula plus blastocyst development (15% and 24% vs. 45%, P 〈 0.05). Cumulus cell co-culture started at various stages had no effect on fertilization and cleavage development but significantly improved rates of embryo development to morula or blastocyst stages (P 〈 0.05). Cumulus cell removal at 20 hr after IVF resulted in similar development to controls (P 〉 0.05) at all stages tested in this study. The intact state of surrounding cumulus cells of oocytes or embryos appears to be beneficial before or shortly after insemination (at or before 7 hr of IVF) but not essential at 20 hr after IVF. © 1995 Wiley-Liss, Inc.
    Additional Material: 5 Tab.
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  • 5
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Electroanalysis 2 (1990), S. 133-137 
    ISSN: 1040-0397
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Flow-injection analysis (FIA) with voltammetric detection can be used in either the direct voltammetric or the stripping mode. In this study, a locally designed and constructed instrument with features not available in commercial instruments was used for the precise analysis of silver in aluminum. The carrier solution was 0.1 M Al(NO3)3 with 2 × 10-3 M HNO3. Silver solution was introduced by timed, partial-loop injection. After cathodic deposition, a square-wave or staircase voltammetric stripping sweep was applied. The data were recorded and analyzed by computer. Silver solutions of 8 × 10-8 to 4 × 10-5 M were tested. The standard deviations of repeat determinations of artificial samples varied from 0.12 to 0.78%. This precision was limited by the stability of the pump flow.
    Additional Material: 4 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Electroanalysis 2 (1990), S. 289-292 
    ISSN: 1040-0397
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Human immunoglobulin G and A (IgG and IgA) were studied with square-wave voltammetry. For IgG, three reduction peaks (HIGG1, HIGG2, and HIGG3) were observed under different conditions. HIGG1 and HIGG3 are strongly related to the pH of the buffer solution. In pH 7.5 phosphate buffer, the peak potential of HIGG2 is -0.58 V (vs. Ag/AgCl). A linear response holds for human IgG below 3.3 × 10-8 M (5 ppm). As little as 1.1 × 10-10 M (16 ppb) of human IgG is detectable after only 20 seconds of adsorptive accumulation in static solution.IgA has two flat adsorptive-stripping responses (HIGA1 and HIGA2). The sensitivity of IgA is much poorer compared to IgG. HIGA2 at -0.44 V can be observed throughout the tested pH range with the maximum response between pH 6.0-6.2. In a static solution, a linear calibration graph can be obtained for 0.8-16.8 ppm IgA.IgG and IgA can be separated from each other by using HPLC with an AB × column. The response of 32 ppb IgG can be observed clearly. This research indicates the possibility of direct separation and detection of immunoglobulins from a real sample (e.g., human serum) by simply applying HPLC-adsorptive-stripping analysis.
    Additional Material: 4 Ill.
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