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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_701R86985004A
中文名称:
英文名称:TRITON X-100 WETTING AGENT
货期:热销品现货,其他请咨询




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文献和实验In Situ HYBRIDIZATION TO TISSUE SECTIONS
/0.3% Triton X-100. Rinse well to remove all food and yeast. Blot well to remove excess liquid. Dechorionate embryos in freshly diluted 50% chlorox for 3' at room temperature with gentle agitation. Rinse with NaCl/Triton; blot well. Transfer
(from R. Plattner & A.M. Pendergast) 1. Following stimulation, place cells on ice and wash 2X with cold PBS 2. Lyse each 100 mm plate with 500-1000 μl of lysis buffer (50mM HEPES pH7.0, 150 mM NaCl, 10% glycerol, 1% triton-X-100, 1.5 mM MgCl
Site‐Specific Protein Labeling with SNAP‐Tags
phosphate‐buffered saline (DPBS; with CaCl 2 and MgCl 2 ; e.g., Invitrogen) Cell lysis buffer: 50 mM Tris·Cl, pH 7.4 ( appendix 2E )/150 mM NaCl/1% (v/v) Triton X‐100/1× protease inhibitors
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