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文献和实验Hot Start activation approaches are increasingly being used to improve the performance of PCR. Since the inception of Hot Start as a means of blocking DNA polymerase extension at lower temperatures, a number of approaches have been developed
使用 Platinum® Taq DNA 聚合酶 (Platinum® Taq DNA Polymerase)，对靶序列进行定性验证
实验步骤 The procedure on the following page is suggested as a guideline and starting point when using Platinum® Taq DNA Polymerase in any PCR amplification. Optimal reaction conditions (incubation times and temperatures
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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