Description
Product Overview
The Azura Genomics TaqMan qPCR Master Mix is engineered for robust, high‑sensitivity detection of both DNA and cDNA targets. Featuring a hot‑start polymerase formulation, the mix reduces non‑specific amplification and primer‑dimer formation, ensuring accurate quantification across a wide range of template complexities, including GC‑rich regions. It is compatible with standard and fast‑cycling qPCR instruments, supporting flexible cycling parameters for diverse assay designs.
Usage
Designed for molecular biology laboratories, this master mix excels in two‑step RT‑qPCR, gene expression analysis, and multiplex qPCR panels. Researchers can employ it in routine diagnostic assays, pathogen detection, and high‑throughput screening where precise quantification is critical. Its broad compatibility makes it suitable for both academic and commercial settings, from small‑scale experiments to large‑scale projects.

Why Choose Us
Azura Genomics combines rigorous quality control with advanced enzyme engineering to deliver a master mix that offers unparalleled sensitivity and specificity. The hot‑start chemistry allows room‑temperature setup, reducing workflow time and error risk. Each batch is validated for performance consistency, providing confidence in reproducible results across experiments.
Key Features
- Hot‑start polymerase minimizes primer‑dimer formation for clean amplification.
- High sensitivity enables detection of low‑abundance targets in complex samples.
- Broad compatibility with standard and fast‑cycling qPCR platforms.
- Optimized for both single‑plex and multiplex assays, supporting up to 5‑plex reactions.
- Room‑temperature assembly simplifies workflow and reduces setup time.
FAQ
Can this master mix be used with GC‑rich templates?
Yes, the formulation is designed to efficiently amplify GC‑rich sequences, providing reliable quantification where traditional mixes may struggle.
Is the mix compatible with fast‑cycling qPCR instruments?
Absolutely. It supports rapid cycling protocols without compromising sensitivity or specificity, making it ideal for high‑throughput applications.
What is the recommended storage condition?
Store the master mix at -20°C. Avoid repeated freeze‑thaw cycles by aliquoting into working volumes as needed.
Does the hot‑start feature require a separate activation step?
No additional activation step is needed; the hot‑start polymerase becomes active during the initial denaturation phase of the qPCR run.
Can this product be used for both DNA and cDNA targets?
Yes, it is optimized for the detection of both genomic DNA and reverse‑transcribed cDNA, making it versatile for gene expression and genotyping assays.





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