• UPta™ Taq PCR Master Mix, lyophilized, 2×

UPta™ Taq PCR Master Mix, lyophilized, 2×

  • Biotechrabbit
  • BR0201301
  • Na skladě
  • 1 026,00 Kč

Dostupné možnosti

- NEBO -

Dopravné a balné

Transportní podmínky                                   cena se připočítává k položkám v objednávce

mražené na suchém ledu (dry ice)                   690 Kč bez DPH na zásilky v celkové ceně do 45 000 Kč bez DPH, nad tuto hodnotu je dopravné a balné zdarma


Features

§  Room-temperature stable enzymes and mixes

§  Aptamer-based hot-start functionality

§  Highest PCR sensitivity without any activation step

§  Optimized Master Mix including exceptionally pure UPta Taq DNA Polymerase and highest quality dNTPs

Applications

§  Ambient shipment and room-temperature storage

§  Fast PCR reactions

§  High-specificity and high-throughput hot-start PCR up to 5 kb

§  Amplification of low-copy-number targets

§  TA cloning

Purchase UPta™ Taq PCR Master Mix, lyophilized, 2×

 

Catalog #

Size

Package Content

BR0201301

50 rxn of 50 µl

Lyo UPta Taq PCR Master Mix
1.25 ml PCR Reconstitution Buffer

BR0201302

250 rxn of 50 µl

5 × Lyo UPta Taq PCR Master Mix
5 × 1.25 ml PCR Reconstitution Buffer

 

Biotechrabbit™ Lyo UPta Taq PCR Master Mix is a freeze dried version of the well-established liquid equivalent. The stabilized format allows shipment and storage without cooling.

UPta Taq PCR Master Mix is a perfect choice for a fast PCR reactions. It reduces the time required for pipetting and eliminates the need for buffer optimization. The mix is optimized for low-background, high-throughput PCR of 0.2–5 kb DNA targets.

The 2x Master Mix contains pure biotechrabbit UTpa Taq DNA Polymerase, extremely high-quality dNTPs and optimized PCR buffer; thus, only template, PCR primers and PCR-grade water are added.

The aptamer binds to Taq DNA Polymerase and inhibits its activity at temperatures below 45°C. This ensures full hot-start functionality. The enzyme is released during standard PCR cycling conditions. There is no need for separate heating or denaturation steps, allowing fast PCR reactions. The hot-start functionality minimizes primer–dimers and mispriming.

 

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