Articles in this section

• Where can I find help troubleshooting my PCR?
• Will the 5'→3' flap endonuclease activity of Taq DNA Polymerase degrade primers?
• When should Taq DNA Polymerase be used in a primer extension reaction or for PCR?
• The product sequence doesn't completely match the expected sequence. How can this result be improved?
• Why is there no product when visualized on an agarose gel?
• What type of DNA end results from a primer extension reaction or a PCR using Taq DNA Polymerase?
• What is the maximum product length that can be made by GenScript's Taq DNA Polymerase?
• What is the proper concentration for a routine PCR reaction?
• How should I set up an amplification reaction using Taq DNA Polymerase?
• Which buffer should I use if I want to control the level of magnesium (Mg2+) in the reaction? Does the presence of Mg2+ inhibit PCR?