Literature DB >> 17194575

An optimized assay for transcription factor NF-kappaB with dsDNA-coupled microplate.

Jian Lin Li1, Hong mei Chen, Min li Li, Dong Hua, Zu hong Lu, Jin ke Wang.   

Abstract

To develop an EMSA-free assay approach for analyzing the sequence-specific DNA-binding proteins (DBPs), an easy cost-effective dsDNA-coupled plate (dcPlate) was developed in our lab for this purpose. In this paper, the assay conditions of such dcPlate were fully optimized for detecting an important transcription factor, NF-kappaB. The optimized parameters of dcPlate for assay of NF-kappaB were as follows: immobilized DNA probe at the concentration of 25 pmol/100 microL-well, incubation time of 90 min for NF-kappaB binding to dcPlate, primary and secondary antibody concentration of 0.1 microL/100 microL dilution, incubation time of 90 min for primary antibody binding to NF-kappaB, temperature of 25 degrees C for the above process, colorimetric developing time for 30 min. After optimization, the signal was improved three times higher than that from not optimized conditions. The linear colorimetric detection ranges of the purified recombinant NF-kappaB p50 and the cell nuclear extract were from 0.59 to 75 ng/well and 0.313 to 10 microg/well, respectively.

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Year:  2006        PMID: 17194575     DOI: 10.1016/j.colsurfb.2006.11.015

Source DB:  PubMed          Journal:  Colloids Surf B Biointerfaces        ISSN: 0927-7765            Impact factor:   5.268


  3 in total

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Journal:  Bioconjug Chem       Date:  2009-07-02       Impact factor: 4.774

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Authors:  Yu-Ling Lin; Yun-Ju Lai; Tai-Chu Peng; Ru-Ping Lee; Kuang-Wen Liao; Nu-Man Tsai; Yen-Ku Liu; Chueh-Jen Tsai
Journal:  Biol Proced Online       Date:  2010-04-14       Impact factor: 3.244

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Authors:  Olha Zhenyukh; Maria González-Amor; Raul R Rodrigues-Diez; Vanesa Esteban; Marta Ruiz-Ortega; Mercedes Salaices; Sebastian Mas; Ana M Briones; Jesus Egido
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  3 in total

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