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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and measure protein concentration (BioRad assay) use 1 - 5 mg protein per IP immunoprecipitate for 2 h to ON, 4 °C wash immunoprecipitations pelleting the beads each time: 2 x 1 ml CHIP lysis buffer 2 x 1 ml CHIP
Fastfilter Plasmid Midi Kit Spin Protocol
130 ul 5M NaCl and 2.2 ml room temperature isopropanol. Vortex to mix and centrifuge at >15,000 x g for 30 min at 4°C. Carefully decant the supernatant. 3. Wash DNA pellet once with 1 ml ice-cold 70% ethanol and centrifuge at > 15,000 x g for 10
Extraction of DNA using DNAzol® Reagent
the cells again and resuspend them in one volume of cold (4°C) hypotonic solution [20 mM Tris HCl (pH 8.0), 10 mM EDTA]. Pellet the cells at 4,000 rpm for 10 min (4°C). Discard the supernatant and add 1 ml DNAzol® per 1-3 × 107 cells. Lyse the cells
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