Literature DB >> 4040719

Adaptation of the dye-binding protein assay to microtiter plates.

M G Redinbaugh, W H Campbell.   

Abstract

The dye-binding protein assay has been adapted for use with microtiter plates and a plate reader. The total volume of the assay was reduced to 0.2 ml, with equal volumes of sample and diluted dye reagent being used. Because of the small volume, the assay is conservative of both protein sample and reagent. The use of microtiter plates allows the absorbance of samples to be read using a plate reader, markedly reducing the time needed for evaluating sample absorbances. This assay is quite sensitive, with a limit of less than 0.5 micrograms bovine serum albumin. In addition, the assay has been calibrated with homogeneous nitrate reductase. The response of nitrate reductase in the assay is about 70% of that of the standard protein, bovine serum albumin. The response of several other proteins was evaluated and the differences in response are discussed.

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Year:  1985        PMID: 4040719     DOI: 10.1016/0003-2697(85)90020-x

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


  16 in total

1.  Purification and some properties of proliferation suppressing factor from human lung adenocarcinoma PC-8.

Authors:  H Shinmoto; S Dosako; K Yamada; S Shirahata; H Murakami
Journal:  Cytotechnology       Date:  1990-09       Impact factor: 2.058

2.  Production and characterization of monoclonal antibodies against the lethal factor component of Bacillus anthracis lethal toxin.

Authors:  S F Little; S H Leppla; A M Friedlander
Journal:  Infect Immun       Date:  1990-06       Impact factor: 3.441

3.  A low-temperature method for the isolation of small-intestinal epithelium along the crypt-villus axis.

Authors:  N Flint; F L Cove; G S Evans
Journal:  Biochem J       Date:  1991-12-01       Impact factor: 3.857

4.  Expression in Escherichia coli of Cytochrome c Reductase Activity from a Maize NADH:Nitrate Reductase Complementary DNA.

Authors:  W H Campbell
Journal:  Plant Physiol       Date:  1992-06       Impact factor: 8.340

5.  Regulation of Corn Leaf Nitrate Reductase : I. Immunochemical Methods for Analysis of the Enzyme's Protein Component.

Authors:  W H Campbell; J L Remmler
Journal:  Plant Physiol       Date:  1986-02       Impact factor: 8.340

6.  Identification of the major antigens of Treponema hyodysenteriae and comparison with those of Treponema innocens.

Authors:  S N Chatfield; D S Fernie; C Penn; G Dougan
Journal:  Infect Immun       Date:  1988-05       Impact factor: 3.441

7.  Monoclonal antibody-based immunoaffinity chromatography for purifying corn and squash NADH: nitrate reductases. Evidence for an interchain disulfide bond in nitrate reductase.

Authors:  G E Hyde; J A Wilberding; A L Meyer; E R Campbell; W H Campbell
Journal:  Plant Mol Biol       Date:  1989-08       Impact factor: 4.076

8.  Production of prostaglandins D2 and E2 by mouse fibroblasts and astrocytes in culture caused by Trypanosoma brucei brucei products and endotoxin.

Authors:  R A Alafiatayo; M R Cookson; V W Pentreath
Journal:  Parasitol Res       Date:  1994       Impact factor: 2.289

9.  Cytosolic phospholipase A2 from human monocytic cells: characterization of substrate specificity and Ca(2+)-dependent membrane association.

Authors:  W Rehfeldt; K Resch; M Goppelt-Struebe
Journal:  Biochem J       Date:  1993-07-01       Impact factor: 3.857

10.  Clinical relevance of cathepsin B-like enzyme activity and cysteine proteinase inhibitor in melanocytic tumours.

Authors:  A Yoshii; T Kageshita; H Tsushima; T Ono
Journal:  Arch Dermatol Res       Date:  1995       Impact factor: 3.017

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