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Is there an advantage in keeping HT in the optimem-Glutamax culture media?
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The original published procedure for Ouchterlony gels included sucrose and EDTA in the agarose. Why? How does it effect the result?
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Using stand monoclonal attachment to plate, followed by 6x washes with PBST, the plate is blocked with 1.2% seablock followed with a 2%sucrose 4%OVO solution block. We have a high background with...
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