赛默飞世尔Thermo Fisher 50X4.6MM 5µ
M HYPURITY ADVANCE column ADVANCE 5µm particle size 50mmx 4.6mm 货号：T_70311592831- ￥1200 - 24000
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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_70311592831
中文名称：
英文名称：50X4.6MM 5µM HYPURITY ADVANCE column ADVANCE 5µm particle size 50mmx 4.6mm
货期：热销品现货，其他请咨询
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文献和实验General Preparation 1. Prepare buffers and have them cold. Make 50X stock of Buffer G and dilute as needed from frozen aliquots of 50X Buffer G. 1X Extraction Buffer without detergents: 1 M Tris-Cl, pH 7.0, 0.6 M KCl, 0.5 mM ATP
Transgenic and Knockout Mice PROTOCOL
analysis). Cool on ice for 5 minutes. Aliquot 18 µl of PCR reaction buffer into a PCR tube PCR Reaction Buffer 1X PCR buffer 2.5 mM MgCl2 200µM dNTPs 1µM each primer 1 Unit
. Cover and let the chamber saturate while loading the plates. 3. With a 10 µl capillary pipette, spot 1-2 µl of phospholipids standard onto the TLC plate, as shown. Make sure the spot remains smaller than 4 mm in diameter
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