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上海玉博生物科技有限公司
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文献和实验.6. Load 10μl- 25μl(10μl for a 15 tooth mini comb) and then overlay samples with 1 x SDS running buffer. Empty wells should have 10-15μl sample buffer added and be overlayed as with the test samples so the gel runs straight. Flood the upper chamber
Differential cDNA Screening Procedures
ul RNasin (Promega) 1 ul M-MLV RT (BRL) 2 ul 1.25X RT Buffer (-dCTP) is: 1.O M Tris-HCl (pH 8.7) 100ul 100mM 100 mM DTT 10 ul 10 mM 1.O M KCl 40 ul 40 mM 1.0 M MgCl2 8 ul 8 mM 100 mM dGTP (Pharmacia) 8 ul 0.8 mM 100 mM dATP 8 ul
核蛋白基因组指纹技术Fine Mapping of Genomic Targets of Nuclear Proteins in Cultured Cells
) and store at 4°C (to avoid DNA precipitation, do not freeze). PCR Analysis 15. Perform the test, negative control, and the input-control (dilutions of 1/10, 1/100, and 1/1000 of the input) PCRs in 25-µl volumes, using
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