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EzPCR™ BASIC Plus 5X Master Mix
EBT-7161 / EBT-7161-5
EBT-7551_1.jpg
EBT-7551_2.jpg
CAT #EBT-7161 / #EBT-7161-5
QTY 1ml (250 rxn / 4㎕) / 5ml (1,250 rxn / 4㎕)

Description 
EzPCRTM BASIC Plus 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. 
  EzPCRTM BASIC Plus 5X PCR Master Mix is amixtureof rTaq DNA polymerase and Pfu DNA Polymerase. rTaq DNA polymerase that is a recombinant thermostable DNA polymerase from Thermus aquaticus has a 5’ à 3’ exonuclease activity. EzPCRTM BASIC Plus 5X PCR Master Mix is recommended for use in conventional PCR process.
  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 rTaq DNA polymerase is contained in 4 ㎕ of 5X Master Mix.

Qualifying Test
 Performance test, exo/endo nuclease contamination test, stability test. genomic DNA contamination test.
 
Storage Condition
  Store at -20 ℃.
  EzPCR™ BASIC Plus 5X PCR Master Mix is stable for at least 1 years at recommended storage condition
 
Standard Experiment Protocol
1. Prepare the 20 ㎕ PCR solution as follows
 
    EzPCRTMBASIC Plus 5X Master Mix
 4 ㎕
    Primer (10 pmol/㎕) 
 each 0.5 ㎕
    Template DNA 
 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 - 20 sec   
10 - 30 sec   
 Anneal
Tm ℃   
10 - 20 sec   
10 - 20 sec   
 Extend
72 ℃   
10 - 30 sec   
30 sec / Kbp   
 
   * Set 25-35 PCR cycles for effective amplification.


 
 

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