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- 详细信息
- 文献和实验
- 技术资料
- 库存:
999
- 供应商:
北京泽平
- 现货状态:
热销品大量现货,其余请咨询
- 保修期:
1年
- 规格:
EA
货号:T_70111-680-24
中文名称:
英文名称:BLOCK 40HOLES 0.5ML CENT TUBES
货期:热销品现货,其他请咨询




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文献和实验Preparation of total RNA from whole blood collected in PAXgene tubes
into a 1.5 ml or 2 ml microcentrifuge tube (not supplied). Add 300 µl Buffer BR2 and 40 µl Proteinase K. Mix by vortexing, and incubate for 10 min at 55℃ using a shakerincubator, heating block, or water bath.If a heating block or water bath is used, vortex
7b. Pool the supernatants from step 6 into 500 ml bottles and add DNase-free RNase A and RNase T1 such that the final concentration of RNase A is 40 ug/ml and RNase T1 is 40 U/ml. Incubate in a 37degC water bath for 30 minutes. 8b. Add an equal
Combined 3C-ChIP-Cloning (6C) Assay: A Tool to Unravel Protein-Mediated Genome Architecture
(from Step 24). Incubate with rotation for 3 h at 4°C. 27. Prechill one 1.5-mL tube for each immunoprecipitate. 28. Transfer ~1.5 mL of each immunoprecipitate to a separate prechilled tube. Place the tubes in the magnetic
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