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I purified my antibody form the blood serum, and kept the antibody in PBS containing 25% glycerol at -80℃ . The antibody was good the first time I used, but It became worse later time by time...
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The bacteria culture became clear when the OD600 is reached about 0.8.
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The protein PI is 9.4, but the running buffer pH8.3, will this be the problem?
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