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- 文献和实验
- 技术资料
- 保存条件:
RT
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见标签
- 库存:
999
- 供应商:
鹿森生物
- 规格:
100mg

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文献和实验Chromatin immunoprecipitation protocol for Saccharomyces cerevisiae
double-strand breaks (DSBs) in budding yeast (Saccharomyces cerevisiae ) (Cobb et al., 2003; van Attikum et al., 2004). Back to top Procedure Preculture of yeast cells for ChIP of proteins at DSBs We have used strains with JKM179
) and resuspend in 1ml pH 7.5 TE buffer ( 0.05 M EDTA, 0.01 M TRIS pH 7.5) 4. Wash twice with pH 7.5 TE buffer. 5. Resuspend in 0.15 ml of pH 7.5 TE with 1 µl zymolyase ( 20 mg/ml in 10 mM sodium phosphate pH 7.5) 6. Add 0.25 ml of 1% low melting agarose
Pulsed Field Gel Electrophoresis
buffer ( 1 hour each wash). 13.Store at 4℃ in 0.05M EDTA, 0.01 M TRIS pH 7.5. Program for Separating Chromosomes of Saccharomyces cerevisiae Size range: 240-2200 kb Agarose: 1.0% electrophoresis agarose Buffer: 0.5x TBE Temperature: 14℃ Switch time
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