DNA Amplification

Hot Start PCR

Hot Start PCR is a technique that reduces non-specific amplification and offers the convenience of reaction set up at room temperature. The polymerases used in Hot Start PCR are unreactive at ambient temperatures. Polymerase activity can be inhibited at these temperatures through different mechanisms, including antibody interaction, chemical modification and aptamer technology. At permissive reaction temperatures reached during PCR cycling, the polymerase dissociates from its inhibitor and commences polymerization. Use of hot start DNA polymerases is most often recommended for high-throughput applications, experiments requiring a high degree of specificity, or even routine PCR where the added security offered by a hot start enzyme is desired.

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FAQs for Hot Start PCR
Protocols for Hot Start PCR
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Hot Start PCR

Deoxynucleotide (dNTP) Solution Mix

Deoxynucleotide (dNTP) Solution Set

EpiMark® Hot Start Taq DNA Polymerase

LongAmp® Hot Start Taq 2X Master Mix

LongAmp® Hot Start Taq DNA Polymerase

NEBNext® Q5® Hot Start HiFi PCR Master Mix

OneTaq® Hot Start 2X Master Mix with GC Buffer

OneTaq® Hot Start 2X Master Mix with Standard Buffer

OneTaq® Hot Start DNA Polymerase

OneTaq® Hot Start Quick-Load® 2X Master Mix with GC Buffer

OneTaq® Hot Start Quick-Load® 2X Master Mix with Standard Buffer

Phusion GC Buffer Pack

Phusion HF Buffer Pack

Phusion Hot Start Flex 2X Master Mix

Phusion Hot Start Flex DNA Polymerase

Q5® Hot Start High-Fidelity 2X Master Mix

Q5® Hot Start High-Fidelity DNA Polymerase

Q5® Blood Direct 2X Master Mix

Q5®-XT Hot Start High-Fidelity 2X Master Mix