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EzPCR™ Basic 2x Premix
EBT-7122 / EBT-7122-5
CAT #EBT-7122 / #EBT-712-5
QTY 96 tube (10 ㎕) / 480 tube (10 ㎕)

Description 
EzPCR™ BASIC 2x PCR Premix 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.
  EzPCR™ BASIC 2x PCR Premix contains rTaq DNA polymerase that is a recombinant thermostable DNA polymerase from Thermus aquaticus. rTaq DNA polymerase has a 5’ à 3’ exonuclease activity and generates a 3’dA overhang. EzPCR™ BASIC 2x PCR Premix is recommended for use in conventional PCR process.
  As Premix is supplied as a 2x concentration format, users should adjust a final reaction to 1x (if final reaction volume is 20 ㎕, 10 ㎕ of 2x Master Mix should be added).
  One unit of rTaq DNA polymerase is contained in 10 ㎕ of 5x Premix
 
Application
  -  Appropriate for standard PCR amplifications.
  - Designed to perform PCR amplification on all DNA templates.
  - Amplification of cDNA and genomic DNA
  - Colony PCR

QC Test
Performance test, exo/endo nuclease contamination test, stability test. genomic DNA contamination test.
 
Storage Condition
Store at -20 ℃. 
 EzPCR™ BASIC 5x PCR Premix is stable for at least 1years at recommended storage condition.

Feature
 - 5’ → 3’ exonuclease : yes
 - 3’ → 5’ exonuclease : no
 - strand displacement : no

Standard Protocol
1. Prepare the 20 ㎕ PCR solution as follows
 
    EzPCR™BASIC 2x Premix
 4 ㎕
    Primer (10 pmol/㎕) 
 each 0.5 ㎕
    Template DNA 
 0.1 - 50 ng
     PCR grade distilled water 
 -㎕
     Add distilled water to make 20 ㎕ final volume.

 2. Set PCR cycling as follows
 
  Initial denature at 95 ℃ : 3 min 
 
 
<  1 kbp
 > 1 kbp
 Denature   
95 ℃    
10 - 30 sec    
30 sec    
 Anneal
Tm ℃    
10 - 20 sec    
30 sec    
 Extend
72 ℃    
10 - 30 sec    
1 min / Kbp    
 
   * Set 25-35 PCR cycles for effective amplification.