赛默飞世尔Thermo Fisher 300 µl Matr
ix DARTs Extended Length, Filtered, 20 Magazines of 96 tips per case, Sterile 货号：5538- ￥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：5538
中文名称：
英文名称：300 µl Matrix DARTs Extended Length, Filtered, 20 Magazines of 96 tips per case, Sterile
货期：热销品现货，其他请咨询
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文献和实验at 95°C, then place them on ice. Load 5-7 µl of each sample into the gel. Run the gel at 400 V for 24 hours at room temperature. In most cases SSCP separates 150- to 300-bp single-stranded DNA fragments with one or more nucleotide differences
to the column and wash the reaction vial with an additional 200-300 µl of fresh TEAB. Add the wash to the column and allow it to begin to run down into the matrix. When the dye product has been absorbed into the matrix, refill the column with buffer and reattach
-stained nucleic acids. b) Weigh the gel slice in a tared tube c) Add 1 ul 50x Gelase buffer per 50 mg of gel (1 ul of molten agarose=1mg of gel) d) Melt the gel slice completely at 70o C e)Equilibrate the molten agarose at 45o C for 20 minutes. f
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