Literature DB >> 3468811

Enzyme activity dot blots: a rapid and convenient assay for acetyltransferase or protein kinase activity immobilized on nitrocellulose.

C D Allis, L G Chicoine, C V Glover, E M White, M A Gorovsky.   

Abstract

Methods are described for assaying (Tetrahymena) histone acetyltransferase activity and (Drosophila) casein kinase II activity by spotting extracts on nitrocellulose filters. The methods are quantitative over a wide range of enzyme concentrations and are almost as sensitive as liquid assays. Examples are presented for illustrating the use of these methods for enzyme purification, concentration, and desalting, as well as for electrophoretic blotting from agarose gels. A simple method for autoradiographic enhancement of nitrocellulose filters is also described.

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Year:  1986        PMID: 3468811     DOI: 10.1016/0003-2697(86)90307-6

Source DB:  PubMed          Journal:  Anal Biochem        ISSN: 0003-2697            Impact factor:   3.365


  2 in total

1.  A single histone acetyltransferase from Tetrahymena macronuclei catalyzes deposition-related acetylation of free histones and transcription-related acetylation of nucleosomal histones.

Authors:  L G Chicoine; R Richman; R G Cook; M A Gorovsky; C D Allis
Journal:  J Cell Biol       Date:  1987-07       Impact factor: 10.539

2.  Micronuclei and the cytoplasm of growing Tetrahymena contain a histone acetylase activity which is highly specific for free histone H4.

Authors:  R Richman; L G Chicoine; M P Collini; R G Cook; C D Allis
Journal:  J Cell Biol       Date:  1988-04       Impact factor: 10.539

  2 in total

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