Literature DB >> 1126852

Evaluation of two protein end-group reactions as potential fluorescent cytochemical methods.

F W Harrison, S K Curtis, R R Cowden.   

Abstract

Histochemical preparations stained by a variant of the Morel-Sisley reaction for protein tyrosine were found to produce a red fluorescence when excited by broadband blue light which is topologically identical to the distribution of chromophore when viewed by absorption (equal transmission) microscopy. The fluorescence mode of viewing preparations stained by this method gave greater sensitivity and contrast than the absorption mode. The p-dimethylaminobenzaldehyde (DMAB)-nitrate method for protein tryptophan did not result in a useful fluorescent end-group method. Preparations stained by this method displayed a pattern of generalized fluorescence of all structures except those which react in the final step of the p-DMAB-nitrite reaction. The specificity of the intermediate reaction product has yet to be established.

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Year:  1975        PMID: 1126852     DOI: 10.1007/bf01004836

Source DB:  PubMed          Journal:  Histochem J        ISSN: 0018-2214


  4 in total

1.  A p-dimethylaminobenzaldehyde-nitrite method for the histochemical demonstration of tryptophane and related compounds.

Authors:  C W ADAMS
Journal:  J Clin Pathol       Date:  1957-02       Impact factor: 3.411

2.  Demonstration of protein-bound sulfhydryl and disulfide groups with fluorescent mercurials.

Authors:  R R Cowden; S K Curtis
Journal:  Histochemie       Date:  1970

3.  Effects of anhydrous benzoylation on staining with a variety of protein end-group methods.

Authors:  S K Curtis; R R Cowden
Journal:  Histochemie       Date:  1970

4.  Fluorescence of 2-hydroxy-3-naphthoic acid hydrazide derivatives of side-chain carboxyl groups of proteins.

Authors:  S K Curtis; R R Cowden
Journal:  Histochemie       Date:  1971
  4 in total

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