Relative Quantitative Assay of the Biological Activity of Interferon Messenger Ribonucleic Acid
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چکیده
منابع مشابه
comparison of catalytic activity of heteropoly compounds in the synthesis of bis(indolyl)alkanes.
heteropoly acids (hpa) and their salts have advantages as catalysts which make them both economically and environmentally attractive, strong br?nsted acidity, exhibiting fast reversible multi-electron redox transformations under rather mild conditions, very high solubility in polar solvents, fairly high thermal stability in the solid states, and efficient oxidizing ability, so that they are imp...
15 صفحه اولThe lack of messenger activity of ribonucleic acid complementary to the viral ribonucleic acid of bacteriophage R17.
RNA complementary to bacteriophage R17 RNA, isolated from bacteria infected with the virus, failed to stimulate protein synthesis in cell-free extracts of Escherichia coli. Under conditions optimal for protein synthesis under the direction of R17 viral RNA, the incorporation of amino acids into peptide linkage in the presence of complementary strand RNA was the same as the incorporation in the ...
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Moses, V. (University of California, Berkeley), and M. Calvin. Lifetime of bacterial messenger ribonucleic acid. J. Bacteriol. 90:1205-1217. 1965.-When cells from a stationary culture of Escherichia coli were placed in fresh medium containing inducer for beta-galactosidase, growth, as represented by increase in turbidity and by total protein synthesis, started within 30 sec. By contrast, beta-g...
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Reovirus single-stranded RNA isolated from mouse L cells pulse-labeled with radioactive RNA precursors for various intervals at different times after infection does not contain detectable poly(A) sequences. All three size classes of viral mRNA, like reovirus double-stranded genome RNA, have cytosine at their 3’ termini. The results indicate that the presence of poly(A) sequences in reovirus sin...
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ژورنال
عنوان ژورنال: Journal of General Virology
سال: 1975
ISSN: 0022-1317,1465-2099
DOI: 10.1099/0022-1317-27-2-225