TATAA SYBR® GrandMaster® Mix – High-Specificity SYBR Green Master Mix for qPCR

TA01-625

Vendor: TATAA Biocenter AB

TATAA SYBR® GrandMaster® Mix – High-Specificity SYBR Green Master Mix for qPCR
€561.75
Maximum quantity available reached.

TATAA SYBR® GrandMaster® Mix is a high-quality, ready-to-use 2X master mix designed for real-time PCR using SYBR Green chemistry. It contains a hot-start DNA polymerase, dNTPs, buffer, and SYBR Green I dye, all optimized to deliver excellent sensitivity, reproducibility, and specificity.

Developed by TATAA Biocenter, this mix ensures minimal primer-dimer formation and background fluorescence, making it ideal for both routine and demanding qPCR applications.

Run your qPCR with maximum efficiency, sensitivity and specificity

The TATAA SYBR® GrandMaster® Mix is a 2x concentrated ready to use fastmix which provides all the necessary components for qPCR, except template and primers. TATAA SYBR® GrandMaster® Mix delivers maximum PCR efficiency, sensitivity, specificity and robust fluorescent signal using fast, or conventional, cycling protocols with SYBR® Green qPCR.

The TATAA SYBR® GrandMaster® Mix is user friendly, does not form bubbles and has an outstanding stability: 6 months in 4°C and 3 months in room temperature.

Suggested applications

  • Gene expression
  • Single-cell analysis
  • Small input amounts
  • Other challenging applications

Features

  • High efficiency for sensitive qPCR analysis
  • Optimised for lower risk of primer-dimer formation
  • Compatible with most qPCR instruments (ROX dye available)
  • Compatible with the PCR Decontamination Kit (ArcticZymes) for 16S targets
  • Robust fluorescent signal using fast, or conventional, cycling protocols with SYBR® Green qPCR 2x concentrated ready to use fastmix

Content

TATAA SYBR® GrandMaster Mix (2x): 2x reaction buffer containing optimized concentrations of: MgCl2 dNTPs Taq DNA polymerase SYBR® Green I Dye Stabilizers

 The number of reactions is based on 20μl-qPCR reactions.

Overview

  •     High-specificity hot-start polymerase minimizes non-specific amplification
  •     Optimized for low background and minimal primer-dimer signal
  •     Suitable for a broad range of targets and template types
  •     Compatible with all major real-time PCR instruments
  •     Ideal for gene expression, validation assays, and quantification

Applications

  •     Gene expression analysis
  •     cDNA quantification
  •     Primer validation
  •     SYBR Green-based screening assays
  •     Educational and clinical research workflows

User Manual

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