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  • Cell & Developmental Biology  (4)
  • Wiley-Blackwell  (4)
  • American Association for the Advancement of Science
  • American Geophysical Union
  • 2015-2019
  • 1980-1984  (3)
  • 1965-1969  (1)
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  • Wiley-Blackwell  (4)
  • American Association for the Advancement of Science
  • American Geophysical Union
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  • 1
    Electronic Resource
    Electronic Resource
    New York, N.Y. : Wiley-Blackwell
    Journal of Cellular Biochemistry 18 (1982), S. 363-375 
    ISSN: 0730-2312
    Keywords: T4 bacteriophage ; short-tail fibers ; fiber formation ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: The characteristics of pure preparations of short-tail fibers of bacteriophage T4 have been studied in the optical and electron microscope. Three main structures were observed: 1) spheres of 8.1 nm diameter; 2) fibers 43 nm long and 3.8 nm thick; and 3) fibers 54 nm long and 3.2 nm thick. Both types of fibers exhibited a regular beaded appearance. The 43-nm fibers were the most abundant structure. During the process of purification of the short-tail fibers, the formation of aggregates was observed each time the material containing the short-tail fibers was dialyzed against saline solutions. These aggregates became increasingly fibrous (as observed in the optical microscope) as the material used was increasingly enriched in short-tail fibers. Finally, most of the aggregates were of the fibrous type when they were formed from a purified preparation of short-tail fibers. In the electron microscope, it was found that the filamentous aggregates were organized in well-defined bundles. The amino acid composition of the highly purified short-tail fibers was also determined. Among the known fibrous proteins, the ones that most resemble the amino acid composition of the short-tail fibers are actin and fibrinogen. These observations are discussed in relation to the T4 short-tail fiber structure and their localization on the hexagonal baseplate of the T4 tail structure.
    Additional Material: 10 Ill.
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  • 2
    Electronic Resource
    Electronic Resource
    New York, N.Y. : Wiley-Blackwell
    Journal of Cellular Biochemistry 25 (1984), S. 109-121 
    ISSN: 0730-2312
    Keywords: adhesion ; cell surface glycoprotein ; monoclonal antibodies ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Two monoclonal antibodies that cause changes in the morphology of cultured chick myogenic cells have been described previously [8]. In this paper, these antibodies are shown to interact with the same 140Kd protein. The 140Kd protein has been further characterized as a cell-surface glycoprotein by lactoperoxidase-catalyzed iodinations and lectin affinity chromatography. The protein is resistant to digestion by trypsin and collagenase and has been shown to be unrelated to fibronectin by immunoprecipitation studies and by peptide mapping. A second protein, of approximately 170Kd MW; is also immunoprecipitated by the monoclonal antibodies. This protein is probably unrelated to the 140Kd protein since the peptide maps are quite distinct.
    Additional Material: 7 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Cellular Physiology 121 (1984), S. 7-12 
    ISSN: 0021-9541
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: We have compared transmembrane potentials (Em) of maternal liver with Em of fetal liver, and as an initial step to account for differences in Em, we have measured intracellular potassium ion activities (aik) in both tissues. Paired segments of maternal and fetal (day 17) mouse liver were suffused (15 ml/min) with Krebs' physiologic salt solution equilibrated with 95% 02 -5% CO2 (pH 7.3-7.4) at 37°C. To measure Em, cells were impaled with open-tip microelectrodes filled with 0.5 M KCI. Intracellular voltage recordings that were stable ± 2 mV for at least 10 s were considered valid impalements. Maternal liver mean Em = - 41 ± 1 (SEM) mV, n = 10 animals. In contrast, fetal liver mean Em = - 23 ± 1 (SEM) mV, n = 10 animals. In the same segments we measured aik with potassium-selective liquid ion-exchanger microelectrodes. Maternal liver mean aik = 95 ± 7 (SEM) mM and fetal liver mean aik = 62 ± 4 (SEM) mM. In addition, Em and aik of fetal liver increased to values comparable to those of maternal liver during the first 8 days of neonatal life. The differences of Em and aik between fetal and maternal liver, and the changes in these values that occur in the neonate, may result from activity of a membrane Na-K exchange pump that increases with tissue development.
    Additional Material: 4 Ill.
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  • 4
    ISSN: 0095-9898
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: The location of sodium and potassium activated Mg-ATPase (Na-K ATPase) was studied in columnar epithelial cells of the small intestine of rats. Cell components were segregated in centrifuge fractions by a mild procedure (sucrose medium), which preserved mitochondria and vesicular inclusions, and by a drastic procedure, designed to preserve the striated borders selectively. The contents of fractions were characterized by phase contrast and electron microscopy and by the assay of alkaline phosphatase (E.C.3.1.3.1), cytochome oxidase (E.C.1.9.3.1), invertase (E.C.3.2.1.26) and Mg-ATPase (E.C.3.6.1.4).Na-K ATPase was found to be most concentrated in fractions containing mitochondria on one hand, and striated borders on the other. Its distribution differed from the distributions of the other four enzymes. The physiological implications of finding the “sodium pump” enzyme in the membrane at the apical pole of the epithelial cell were discussed.
    Additional Material: 4 Ill.
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