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文献和实验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
product is obtained. 5.Taq DNA Polymerase. Usually 1-1.5u of Taq DNA Polymerase are used in 50µl of reaction mix. Higher Taq DNA Polymerase concentrations may cause synthesis of nonspecific products. However, if inhibitors are present in the reaction
实验步骤 1. Measure out the amount of Taq DNA polymerase needed. When using a reaction cocktail, determine the total number of units in the mix. 2. Add an amount of “equivalent units” of Platinum® Taq
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