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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_70103-251-685
中文名称:
英文名称:15CTW900MGSO4 300PSA150GC 10PK
货期:热销品现货,其他请咨询








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文献和实验8.0 0.5% N-propyl gallate 90% Glycerol Store at 4oC PM Buffer* 100 ml 1 M PIPES (100 mM PIPES pH= 6.9) 2 ml 1 M MgSO4 , (2 mM MgSO4 ) 2 ml 0.5 M EGTA (1 mM EGTA,) distilled water to 900 ml adjust pH to 6.9 distilled water
In Situ HYBRIDIZATION TO TISSUE SECTIONS
' in distilled water - Impregnate 15 - 30' in Fluorohance (RPI; or comprable enhancer) - Dry and autoradiograph - Optimal size 75-150 bp Preparation of probe for hybridization (use at 2-20ng/ml) - Precipitate 125mg carrier DNA per 0.5mg 3H-probe (dry ice
ChIP protocol for X. laevis Lens1/FoxE3 enhancer
(1) Remove vitelline membrane from stage 21-23 embryos (n = 300). Collect head tissues (about anterior 1/4 or 1/3 of the embryo) in 1x MBS. (2) Fix the tissues in 0.5x MBS/1% formaldehyde (4-5 ml in a screw cap glass vial) for 15 min
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