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- 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_70312602835
中文名称：
英文名称：Immersion PC201 with bridge Temperature: 200 ° C
货期：热销品现货，其他请咨询
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文献和实验Combined 3C-ChIP-Cloning (6C) Assay: A Tool to Unravel Protein-Mediated Genome Architecture
7 mL of 1.15X ligation buffer. 19. Add 400 µL of 20% Triton X-100 (to a final concentration of 1%). Incubate with occasional gentle shaking for 1 h at 37°C. 20. Add 50 µL of T4 DNA ligase. Incubate for 4 h at 16°C
【转贴】immunofluorescence staining
-T for 30 sec. to 1 min. Remove DAPI and add TBS-T.Part 4: Mounting the CoverslipsLabel slides using a marker designed for slides - pencil can be difficult to read in the microscope room, and immersion oil can smear some ink markers. If using SlowFade
running matrix: To make approximately 200 ml, pour 200 ml of 10 mM TEAB into an Erlenmeyer flask. Add approximately 50 g of Sephadex G-50 and swirl to absorb the liquid. Suspension will settle. Store at 4°C. Prior to use, apply vacuum pressure to the flask
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