bioRxivBiochemistryPreprint
A toolbox of immunoprecipitation-grade monoclonal antibodies against human transcription factors.
Anand VenkataramaniD, Kun YangiD, Jose Irizarry, Mark Mackiewicz, Paolo MitaiD, Zheng Kuang, Lin Xue, Devlina GhoshiD, Shuang Liu, Pedro Ramos, Shaohui Hu, Diane Bayron, Sarah KeeganiD, Richard Saul, Simona Colantonio, Hongyan Zhang, Florencia Pauli Behn, Guang SongiD, Edisa Albino, Lillyann Asencio, Leonardo Ramos, Luvir Lugo, Gloriner Morell, Javier Rivera, Kimberly Ruiz, , Seth BlackshawiD
Abstract
A key component to overcoming the reproducibility crisis in biomedical research is the development of readily available, rigorously validated and renewable protein affinity reagents. As part of the NIH Protein Capture Reagents Program (PCRP), we have generated a collection of 1406 highly validated, immunoprecipitation (IP) and/or immunoblotting (IB) grade, mouse monoclonal antibodies (mAbs) to 736 human transcription factors. We used HuProt human protein microarrays to identify mAbs that recognize their cognate targets with exceptional specificity. Using an integrated production and validation pipeline, we validated these mAbs in multiple experimental applications, and have distributed them to the Developmental Studies Hybridoma Bank (DSHB) and several commercial suppliers. This study allowed us to perform a meta-analysis that identified critical variables that contribute to the generation of high quality mAbs. We find that using full-length antigens for immunization, in combination with HuProt analysis, provides the highest overall success rates. The efficiencies built into this pipeline ensure substantial cost savings compared to current standard practices.
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