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Multiple Transcription Factor Profiling by Enzyme-Linked Immunoassay
Author(s) -
Zeyang Shen,
J. Peedikayil,
Grant Olson,
Paul D. Siebert,
Y. Fang
Publication year - 2002
Publication title -
biotechniques
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.617
H-Index - 131
eISSN - 1940-9818
pISSN - 0736-6205
DOI - 10.2144/02325dd07
Subject(s) - immunoassay , transcription factor , microbiology and biotechnology , electrophoretic mobility shift assay , biology , transcription (linguistics) , dna , enzyme , promoter , e box , gene expression , gene , antibody , genetics , biochemistry , enhancer , linguistics , philosophy
Transcription factor-DNA interactions have been widely studied in the regulation of gene expression. We have established an enzyme-linked immunoassay platform to quantify specific transcriptionfactor-DNA interactions. In our assay, dsDNA immobilized on a 96-well plate captures the transcriptionfactor from the nuclear extract of mammalian cells. The DNA-bound transcription factor is detected and quantified by enzyme-linked immunoassay using a transcription factor-specific antibody. We have profiled multiple transcription factors involved in inflammation including NFkappaB p50, NFkappaB p65, c-Rel, c-Fos, CREB-1, and ATF-2. When compared with the traditional electrophoretic mobility shift assay, the enzyme-linked immunoassay shows a 10-fold higher sensitivity, eliminates the use of radioactivity, allows for a high-throughput format, and is faster.

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