DNA Amplification and PCR

Taq DNA Polymerase is now supplied with -inhibitor free- DNA Loading buffer IF

• Best choice for colony PCR
• Adds a single deoxyadenosine (A) to the 3′- ends of PCR products
• No detectable 3’→5′ proofreading exonuclease activity
• For standard PCR where proofreading is not required
• Excellent cost-performance ratio 

Concentration: 5U/µL
Source: Purified from an E. coli strain carrying a plasmid with Taq DNA polymerase gene from Thermus aquaticus YT-1.
Reagents supplied with: 10x Taq polymerase buffer and 10x DNA Loading buffer IF -inhibitor free-
Store at: -20 °C