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Quantitative Proteinbestimmung in Einzelzellen mit Amidschwarz

Authors :
Schauenstein, E.
Desoye, G.
Nöhammer, G.
Source :
Histochemistry and Cell Biology; January 1980, Vol. 68 Issue: 1 p75-90, 16p
Publication Year :
1980

Abstract

In aqueous solution Amido Black B (ASB) forms stable and well-defined complexes with bovine serum albumin (RSA) at pH 5.5. The complexes can be separated by column chromatography. The formation of the complexes consists in a fast reaction during which, after 3 to 5 h approximately, 3 molecules of ASB have been bound per molecule RSA, and of a much slower reaction which, even after a laps of 24 h, is still far from approaching its final stage. With solid films of RSA, after denaturation with ethanol, fast reaction is found to approach its final stage after 10 min reaction time. With these model protein preparations, the molar extinction coefficient of the ASB-protein complexes can be determined: the soluble ASB-RSA complexes can be brought to complete dissociation at pH 12.3. After the additivity of the specific absorptions of both RSA and ASB had been proven, it was possible to determine the content of the solution of ASB and RSA, and therefrom the molar extinction coefficient of the ASB-RSA-complex at pH 5.5: e<subscript>620</subscript>=110,000. ASB-stained ethanolfixed RSA films show an e<subscript>620</subscript> of approximately 96,000, if their thickness and specific weight are known.

Details

Language :
English
ISSN :
09486143 and 1432119X
Volume :
68
Issue :
1
Database :
Supplemental Index
Journal :
Histochemistry and Cell Biology
Publication Type :
Periodical
Accession number :
ejs16171814
Full Text :
https://doi.org/10.1007/BF00498503