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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_70311382073
中文名称:
英文名称:ACCL TRINITY P1 3µM 2,1X50MM Trinity P1 analytical 2.1mm x 50mm particle size
货期:热销品现货,其他请咨询




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文献和实验) Add 50-200µl affinity-purified antibody (50-100µg immunoglobulin) to 100-200µg unfixed chromatin and add Incubation buffer (50mM NaCl, 20mM Tris-HCl, pH 7.5, 20mM Na butyrate, 5mM Na2 EDTA, 0.1mM PMSF) to a final volume of 1ml (see note 8);
or columns. The method works very well for doing analytical restriction digests of PAC clones and can be scaled up if necessary. Solutions P1 (filter sterilized, 4oC) 50mM Tris, pH 8 10 mM EDTA 100 ug/ml RNase A P2 (filter sterilized, room temp
Whole-mount in situ hybridization for the detection of RNA in C. elegans embryos
Hybridization buffer for cDNA-derived probes: 100 µg/ml autoclaved salmon sperm DNA, 50 µg/ml heparin, 0.1% Tween 20, 50% formamide, 5 X SSC. [ If you are using Wheaton jars that hold up to 20 slides in 150 ml, you will need a total of 1 liter of HYB buffer
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