Tento e-shop využívá cookies

Na našich webových stránkách používáme soubory cookies. Některé z nich jsou nezbytné, zatímco jiné nám pomáhají vylepšit tento web a váš uživatelský zážitek. Souhlasíte s používáním všech cookies?

Cookies nastavení

Vaše soukromí je důležité. Můžete si vybrat nastavení cookies níže.

ALLin™ Mega HiFi Red Mastermix, 2X , 500 r of 50 µl

Kód produktu: HLM0305 Kód výrobce: HLM0305 Výrobce: highQu GmbH professionally simple
-4 %
Ušetříte
957,72 Kč
25 858,31 Kč
24 900,59 Kč
20 579,00 Kč bez DPH
do týdne
500

ALLin™ Mega HiFi Red Mastermix, 2X , 500 r of 50 µl

Zobraz detailní popis

Detailní popis

Applications


  • Fast high-fidelity PCR (up to 100 x Taq)

  • Long PCR up to 20 kb

  • Direct gel loading option

  • Amplification of complex (GC/AT-rich) templates

  • Sequencing, including NGS

  • Blunt-end cloning and other applications



  •  
  •  

Benefits


  • Fast, high yield PCR with the fidelity 100x higher than Taq

  • Up to 20 kb long PCR even from complex templates

  • Increased processivity for faster amplification and higher yield

  • High thermostability for better denaturation of GC rich templates

  • Best choice for NGS and other sequencing applications

  • Red master mix for direct gel loading, supplied with water

Description

Derived from our HiFi polymerase, the highQu ALLin™ Mega HiFi DNA Polymerase, 2 u/µl provides much lower error rate PCR with a 100 higher fidelity compared to Taq. The ALLin™ Mega HiFi DNA Polymerase is engineered to be much faster and to generate a higher yield of long PCR products up to 20 kb from complex GC-rich templates. Therefore the ALLin™ Mega HiFi DNA Polymerase is an excellent choice for longer and very complex PCR applications where the highest fidelity is demanded. It is an enzyme of choice for cloning and all kind of sequencing applications including NGS. Generated blunt-ended PCR products are suitable for ligation into blunt vectors. However, to increase ligation efficiency, the use of HighEnd™ Repair Kit (HER0101) is recommended for final polishing of PCR fragment ends.

The convenience of ALLin™ Mega HiFi DNA Polymerase is maximized by the use of 2X Red Mastermix providing the advantage of reduced pipetting and direct gel loading. ALLin™ Mega HiFi Red Mastermix, 2X is premixed with red dye and density reagents for direct loading on the gels after the PCR. In a 2% agarose TAE gel the dye migrates with~350 bp DNA, in 1% agarose TAE gel with ~ 600 bp DNA fragments. The master mix is even supplied with PCR Water, and the only thing to add is the template with primers.


Protocols:

Important Notes
  • Take typical measures to prevent PCR cross over contamination, keep your bench clean, wear gloves, use sterile tubes and filter pipet tips.
  • Include a no-template control and positive control in parallel.
  • Thaw and keep reagents on ice. Mix well before use.
  • For complex, GC rich templates, use 99-100°C denaturation temperature, it might help to increase the yield.
  • For established PCRs, try two-step cycling protocol with a combined annealing-denaturation step of 70°C (68°C to 75°C).
  • Run an annealing temperature gradient (2°C increments) from 60°C to 66°C to choose the best conditions.
  • The longer the amplicon, the longer the extension time: depending on the complexity of the template, perform extension from 10 sec/kb to 30 sec/kb. Longer extension for more complex templates is needed.

 

Prepare a 50 µl PCR reaction

 

Rev. & For. Primers variable, To 0.2 - 0.6 µM each (~2µl of 10 µM)
cDNA Template or
gDNA Template
<100 ng or
10 - 200 ng
PCR Water to 25 μl
ALLin™ Mega HiFi Red Mastermix, 2X 25 µl

 

  • Mix gently, avoid bubbles
  • Place into the instrument set like:

 

Initial denaturation 1 cycle: 95°C - 1 min
Denaturation 25-35 cycles: 95°C - 15 sec
Annealing 25-35 cycles: 60-66°C- 15 sec
Extension

25-35 cycles: 72°C – 30 sec (10-30 sec/kb)

 

  • After the PCR store probes shortly on ice, for long term store at -20°C.
  • Load probes directly on the agarose gel. ALLin™ Mega HiFi Red Mastermix, 2X is premixed with red dye and density reagents for direct loading after the PCR. In a 2% agarose TAE gel the dye migrates with~350 bp DNA, in 1% agarose - with ~ 600 bp DNA.

Hodnocení produktu

Produkt zatím nikdo nehodnotil, buďte první!