Pfu Super 5x PCR Master Mix
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1 ml (250 rxn/20 ㎕)
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Pfu Super 5x PCR Master Mix is a ready-to-use premix containing all the components essential for a PCR and agarose gel electrophoresis (DNA polymerase, dNTP, reaction buffer, glycerol, bromophenol blue, and stabilizer). PCR can be performed simply by adding primer pair and template.

As Master Mix is supplied as a 5x concentration format, users should adjust a final reaction to 1x (if final reaction volume is 20 ㎕, 4 ㎕ of 5x Master Mix should be added).
One unit of Pfu Super DNA polymerase is contained in 4 ㎕ of 5x Master Mix.

Pfu Super DNA Polymerase is suitable for a reliable amplification of long (up to 15 kbp) and complex targets with a robust yield and high accuracy.
The error rate of Pfu Super DNA Polymerase is two times more less than that of Pfu DNA polymerase.

The amplification efficiency (final yield) is about 2-3 times more than that of Pfu DNA polymerase.
Furthermore, due to its high processivity, shorter running time is required compared to any other commercially available Pfu (5 kbp within 60 sec extension).

The amplified products by Pfu Super DNA polymerase can be used for a gene cloning with highly decreased error rate, and for a site-specific mutagenesis.
Pfu Super DNA Polymerase, like any other polymerases showing proof-reading activity, generates a PCR product with blunt end.

Pfu Super DNA Polymerase exhibits 3´->5´ exonuclease (proof-reading) activity, but has no detectable 5´->3´ exonuclease activity.

QC tests
- Performance tests, genomic DNA contamination test, confirmation test for the absence of endo and exonucleases.

Storage Condition
- Store at -20°C. Pfu Super 5x PCR Master Mix is stable for at least 2 years at recommended storage condition.

Standard Protocol

1. Prepare 20 ㎕ PCR solution as follows:
PCR grade distilled water : - ㎕
Pfu Super 5x PCR Master Mix : 4 ㎕
Primer (10 pmol/㎕) : 0.5 ㎕ each
Template : 0.1-10 ng
Adjust final vol. to 20 ㎕ with PCR grade distilled water

2. Set PCR cycling as follows :
Initial denature at 95°C : 3 min
Denature : 95°C 10 sec
Anneal : Tm-4°C 10 sec
Extend : 72°C 20 sec/1 kbp

* Set 25-35 PCR cycles for effective amplification
* You can also use two step cycle amplification (denaturation at 95°C and annealing/extension at 68°C)

3. You can analyze PCR products by direct loading into agarose gel because PCR Master Mix

contains glycerol and bromophenol blue (blue color) essential for a gel loading. 



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