PCRBIO HS Taq Mix Red
PCRBIO HS Taq Mix Red is an advanced antibody-mediated hot start DNA polymerase mix designed for fast, highly specific and sensitive PCR. The mix contains a red dye allowing reactions to be directly loaded onto agarose gels without additional loading buffer. Whether you need a hot start assay for high-throughput or the detection of a low copy number template, PCR Biosystems offers you a robust industry-leading 2x mix.
A ready-mix with a red dye for easy pipetting
Can handle even GC-rich fragments
Outperforms competitors on 1kb target
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Good HS MM
Agarose PCR
We regularly use PCRBio HS mastermix in our PCR lab for high throughput classical PCR screening where we want consistent methodology with prior experiments. It is great, everything you'd want in standard HS mastermix. Prices used to be the best in the market too, and are now still pretty good.
Review Date: 7 Nov 2024 | PCR Biosystems
PCRBIO HS Taq Mix Red is a ready-to-use 2x mix containing all reaction components apart from primers and template. The mix is powered by PCRBIO HS Taq Mix DNA Polymerase, an advanced antibody-mediated hot start enzyme engineered for fast, highly specific and sensitive PCR. The latest developments in polymerase technology and buffer chemistry enhance PCR speed, yield and specificity, giving a consistently high performance on a broad range of templates including both GC and AT-rich sequences.
Proprietary antibodies inhibit polymerase activity until an initial activation step at 95 °C, preventing the formation of primer dimers and non-specific products, giving improved specificity and sensitivity compared to other methods. The enzyme and buffer system allow for superior PCR performance on complex templates such as mammalian genomic DNA. Whether you need a hot start assay for high-throughput, automated reaction setup or the detection of a low copy number template, PCR Biosystems offers you a robust industry-leading enzyme to meet your needs.
Features
- Ready-to-use 2x mix with preloaded red dye for direct gel loading.
- Increased PCR success rates with amplicons up to 6kb
- Ultra low background DNA
- Advanced buffer chemistry including Mg and dNTPs
- High yields under standard and fast PCR conditions
- Efficient specific amplification from complex templates including GC and AT-rich sequences
