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PMID: 2415018 Published · ppublish English Journal Article

Microassay for proteins on nitrocellulose filter using protein dye-staining procedure.

Analytical biochemistry ·Vol. 148 ·No. 2 ·1985-08-01 ·Pages 311-9

Nakamura K, Tanaka T, Kuwahara A, Takeo K

Abstract

A simple and rapid microassay for proteins utilizing the protein dye-staining procedure with a nitrocellulose (NC) filter is described. Proteins were directly bound to an NC filter using the "BIO DOT" microfiltration apparatus to ensure their uniformity. The proteins were then stained with a dye (Ponceau Red 3R or amido black 10B), and the optical density of the stained protein spots was directly measured by a densitometer. A good linearity between the optical density and the amount of protein was obtained in the range 0.05 to 10 micrograms. A larger number of samples (up to 96 samples) could be assayed within 1.5 h simultaneously. Contaminating chemicals, such as amino acids, sugars, reducing agents, chelating agents, tris(hydroxymethyl)aminomethane, deoxyribonucleic acid, and nucleotides, did not interfere with the assay. The reproducibility, pH dependency, and application of the assay to the quantitation of a small amount of proteins in body fluids are discussed.

MeSH Terms
Adult Blood Proteins/analysis Collodion Coloring Agents Filtration Humans Hydrogen-Ion Concentration Microchemistry Staining and Labeling
Chemicals
Blood Proteins Coloring Agents Collodion
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Nakamura K
Tanaka T
Kuwahara A
Takeo K
Article Info
Journal
Analytical biochemistry
Abbr.
Anal Biochem
ISSN
0003-2697
Published
1985-08-01
Pages
311-9
Language
English
Region
United States
NLM ID
0370535
Subset
IM
Analysis Services
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