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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_70315113037
中文名称：
英文名称：Heating block base SHB1000BASE Stuart large
货期：热销品现货，其他请咨询
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文献和实验Reaction Mixture as follows: 7. Boil reaction in heating block for 5 min. Note: be sure block wells are filled with H2O. 8. Centrifuge briefly to collect condensation. 9. Add 10μl 5X prime dCTP buffer to reaction mix. 10. Add 5μl labeled
QUALITATIVE ANALYSIS OF DNA FRAGMENTATION BY AGAROSE GEL ELECTROPHORESIS
by adding 10x loading buffer to a final concentration of 1x. The addition of loading buffer to samples allows to load gel wells more easily and to monitor the run of samples. 18. Place samples in a heating block at 65°C for 10 min and immediately load 10
seconds. Allow the film to air dry. Each base-specific fluorescent-labeled cycle sequencing reaction routinely included approximately 100 or 200 ng Biomek isolated single-stranded DNA for A and C or G and T reactions, respectively. Double-stranded cycle
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