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- 文献和实验
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5 ml
保存条件:-20℃
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文献和实验of a master mix containing water, buffer, dNTPs, primers and Taq DNA Polymerase in a single tube, which can then be aliquoted into individual tubes. MgCl2 and template DNA solutions are then added. This method of setting reactions minimizes the possibility
DNA聚合酶Taq Plus和 Taq Plus I 有什么区别吗?对PCR结果有影响吗? Taq Plus 集扩增效率高和保真度好于一体。能有效地扩增10 kb以下的片段,扩增效率比Pfu高,保真度 Taq Plus 比Taq好。对于有些结构复杂的模板,如GC含量高、有二级结构等可选用Taq Plus扩增。 Taq
This is a protocol from Engelke et.al.(1990)which was modified by Dr.Baron.The enzyme has been used for RT-PCR,genotyping and cloning.Solutions1000X IPTG0.5M IPTG 1.19g IPTGup to 10 ml wih sterile Qfilter and store at -20℃Buffer A50 mM Tris 7.9 25








