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"Hot Start", Non−"Proofreading"

For all PCR reactions strictly requiring "HotStart" conditions (e.g. fingerprinting with fluorescent detection, multiplex PCR etc.).

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Perpetual Taq Master Mix

"Hot Start" Taq DNA polymerase, MAB inhibited.
  • Fluorescent PCR methods, genotyping, diagnostic PCR.
  • No "proofreading".
  • Convenient, stable master mix.
  • Contains separate, optional Color Load solution for direct gel loading.

Color Perpetual Taq Master Mix

"Hot Start" Taq DNA polymerase, MAB inhibited.
  • Fluorescent PCR methods, genotyping, diagnostic PCR.
  • No "proofreading".
  • Convenient, stable master mix.
  • Mix supplemented with two tracer dyes for direct gel loading.

d-UTP PCR Master Mix (2x) - ON Taq

Carryover-contamination protected "Hot Start" PCR Master Mix, chemical mediated "Hot Start".
  • dTTP is partially replaced by dUTP.
  • UNG treatment prevents carryover PCR contamination ("false positives") by lab-enriched PCR amplicons.

d-UTP PCR Master Mix - Perpetual Taq

Carryover-contamination protected "Hot Start" PCR Master Mix, monoclonal Anti-Taq antibody.
  • dTTP is partially replaced by dUTP.
  • UNG treatment prevents carryover PCR contamination ("false positives") by lab-enriched PCR amplicons.

NXT Taq - Fast PCR Kit

Fast "Hot Start" Taq DNA polymerase, MAB inhibited.
  • "High throughput" genotyping, diagnostic PCRs.
  • No "proofreading".
  • Convenient, stable master mix.
  • Contains separate Color Load solution for direct gel loading.

NXT TiTaq - Fast PCR Kit

Ready-to-use solution for fast PCR containing "hot start" NXT tiTaq DNA Polymerase (Hot Start with thermal dependent inhibitor), reaction buffer, MgCl? and dNTPs. NXT Taq PCR Kit is designed for fast-cycling PCR on any thermal cycler.

M3 Multiplex Master Mix - PCR

"Hot Start" Taq DNA polymerase, MAB inhibited.
  • Multiplex PCR optimized (many targets per assay).
  • No "proofreading".
  • Convenient, stable master mix.
  • Contains separate, optional Color Load solution for direct gel loading.

HRM PCR Master Mix

For detection of gene mutations and SNPs by HRM analysis.

ON Taq PCR Master Mix HOT START

Chemically inhibited "Hot Start" Taq DNA polymerase.
  • Chemical inhibition.
  • Taq inhibitor denaturation is irreversible.
  • Taq contains specific, genetic modifications.
  • Extremely tight "Hot Start".

TI Taq PCR Master Mix HOT START

Cost-effective "Hot Start" Taq DNA polymerase.
  • Thermal dependent inhibitor (TI).
  • Pol. inhibitor denaturation is reversible.
  • Comparable performance to Perpetual Taq at reduced costs.