BM Labosis'e Hoşgeldiniz


tiOptiTaq PCR Master Mix (2x)


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tiOptiTaq PCR Master Mix (2x)
100 Rxn 81 EUR
+%8 KDV
699,84 TL
tiOptiTaq PCR Master Mix (2x)
200 rxn 156,6 EUR
+%8 KDV
1.353,02 TL
tiOptiTaq PCR Master Mix (2x)
500 Rxn 324 EUR
+%8 KDV
2.799,36 TL


• tiOptiTaq PCR Master Mix (2x) is a ready-to-use solution containing tiOptiTaq DNA Polymerase, optimized reaction buffer, MgCl2 and dNTPs.

• Use of tiOptiTaq PCR Master Mix (2x) allows to save time and reduce contamination risk due to fewer pipetting steps during PCR set-up.

• tiOptiTaq DNA Polymerase is a new generation „hot start” enzyme blend that is blocked at moderate temperatures and allows room temperature reactions setup.

• The polymerase activity is restored during normal cycling conditions.

• Use of tiOptiTaq DNA Polymerase allows for the enormous increase of PCR specificity, sensitivity and yield in comparison to the conventional PCR assembly method.

• tiOptiTaq DNA Polymerase catalyzes the polymerization of nucleotides into duplex DNA in the 5'→3' direction in the presence of magnesium ions and exhibits the 3'→5' proofreading activity, resulting in considerably higher PCR fidelity and processivity than possible with unmodified Taq DNA polymerase.

• Enables increased amplification product yield in comparison with Taq DNA polymerase over wide range of PCR products. • Maintains the 5'→3' exonuclease activity.

• Adds extra A at the 3' ends. • tiOptiTaq PCR Master Mix (2x) is recommended for use in PCR and primer extension reactions at elevated temperatures to obtain a wide range of DNA products up to 20 kb.

tiOptiTaq PCR Master Mix (2x) contains:

• tiOptiTaq PCR Master Mix (2x)

Water, nuclease free

• 10 x Color Load

tiOptiTaq PCR Master Mix (2x)

:tiOptiTaq DNA Polymerase is supplied in 2 x Pol Buffer B containing 3 mM MgCl2, 0.4 mM of each dNTP.

10 x Color Load:

10 x Color Load contains two gel tracking dyes and a gel loading reagent. It enables direct loading of PCR products onto an agarose gel.

Quality Control:

All preparations are assayed for contaminating endonuclease, 3'-exonuclease, and nonspecific single- and double-stranded DNase activities. Typical preparations are greater than 95% pure, as judged by SDS polyacrylamide gel electrophoresis.

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