Impact of immunization technology and assay application on antibody performance--a systematic comparative evaluation

免疫技术和检测应用对抗体性能的影响——系统的比较评估

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作者:Michael C Brown, Tony R Joaquim, Ross Chambers, Dale V Onisk, Fenglin Yin, Janet M Moriango, Yichun Xu, David A Fancy, Erin L Crowgey, Yida He, James W Stave, Klaus Lindpaintner

Methods

peptide antigens (3 per protein), DNA prime/protein fragment-boost ("DNA immunization"; 3 per protein), and full length protein. Antibodies thus generated were systematically evaluated using several different assay technologies (ELISA, IHC, and Western blot). Antibodies raised against peptides worked predominantly in applications where the target protein was denatured (57% success in Western blot, 66% success in immunohistochemistry), although 37% of the antibodies thus generated did not work in any of these applications. In contrast, antibodies produced by DNA immunization performed well against both denatured and native targets with a high level of success: 93% success in Western blots, 100% success in immunohistochemistry, and 79% success in ELISA. Importantly, success in one assay method was not predictive of success in another. Immunization with full length protein consistently yielded the best

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