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You are here : PCR / DNA Amplification » Standard-PCR Master Mixes / RTU mixes » Taq DNA Polymerase 2X-preMix

Taq DNA Polymerase 2X-preMix

Maximo Tag Polymerase as 2X-preMix includes all components (Taq DNA polymerase, dNTPs, MgCl2, and reaction buffer) in an optimal concentration for routine PCR

Cat.-no Description Amount Price € Shop
 S113   Maximo Taq DNA Polymerase 2X-preMix  1x100 rcs
 (2x1.25 ml)
     40.00  add
 S114   Maximo Taq DNA Polymerase 2X-preMix  10x100 rcs
 (20x1.25 ml)
   350.00  add
 S114X   Maximo Taq DNA Polymerase 2X-preMix  other amounts  on request  

Maximo Taq DNA Polymerase 2X-preMix:Order/request by E-mail:
Maximo Taq DNA Polymerase 2X-preMix: Datasheet
Maximo Taq DNA Polymerase 2X-preMix: Deutsche Beschreibung

Features:
Maximo Taq DNA Polymerase 2X-preMix provides robust PCR performance in a wide range of PCR applications and different templates. Best value in terms of cost per unit. The optimized mixture of all components reduces pipetting mistakes and ensures repeatable results - every day.

Applications:
- Standard / General PCR
- optimized for high specifity
- High-throughput PCR, automated pipetting, or plate based PCR
- Gene mutation
- T/A cloning

Description: 
Maximo Taq DNA Polymerase 2X-preMix is optimized and ready-to-use mixture of all components for a successful PCR. Only your primers and your DNA Template has to be added. 
Maximo Taq DNA Polymerase 2X-preMix contains a thermostable DNA polymerase that possesses a 5´→3´ polymerase activity and a double-stranded specific 5´→3´ exonuclease activity. The enzyme consists of a single polypeptide with a molecular weight of 94kDa.

Concentration:
  the mixture is 2X concentrated

Unit definition:
One unit incorporates 10 nmol of deoxyribonucleotide into acid-precipitation material in 30min at 74 degree

List of components:
0.1U/ul Taq DNA Polymerase, 0.4 mM dATP, 0.4 mM dGTP, 0.4 mM dCTP, 0.4 mM dTTP, 4 mM MgSO4, 20 mM KCl, 16 mM (NH4)2SO4, 20 mM Tris-HCl, pH8.8

Quality control: 
- PCR with various templates – genomic DNA, Phage Lambda DNA
- 2 kb DNA amplification from 50 ng DNA
- batch variation and level of bacterial DNA contamination
 
Transportation: 
on blue ice


Storage:
at -20°C for 24 months

Usage:  

Components Volume per reaction
 2X Taq mastermix  25 µl
 Up-stream primer (10 µM stock)  0,5-2.5 µl
 Down-stream primer (10 µM stock)   0.5-2,5 µl
 Template DNA  0.1-15 ng/ml plasmid DNA
 1-10 µg/ml genomic DNA
 Sterile dest. Water (molecular grade)  up to 50 µl total reaction volume

Note: 
- vortex all solutions and spin down carefully before using
- dispense on ice and spin down again
- may you have to optimize the MgCl2 concentration for best result

General Thermo-Cycler protocol:

 Step  Time  Temperature
 Initial denaturation  1-5 min  94-95°C
 
25-30 Cycles:
 Denaturation
 Annealing
 Extension
 
 10-25 sec
 10-25 sec
 60 sec

 94-95°C
 45-70°C
 68-72°C per 1kb
 
 Final extension    5 min  68-72°C



 

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Overview Polymerases:

DFS-Taq Polymerase DNA-free
Tag Polymerase (DNA free) is a highly purified polymerase (DNA-free) especially for PCR reactions where freedom from endogenous template (i.e., E. coli DNA) is essential
Taq Polymerase
Maximo Tag Polymerase is a highly purified polymerase for routine amplification
Taq Polymerase 2X-preMix
Maximo Tag as 2X-preMix includes all components (Taq DNA polymerase, dNTPs, MgCl2, and reaction buffer) in an optimal concentration for routine PCR
Taq  Polymerase blue ready-to-load
Maximo Tag-Blue is a highly purified polymerase for routine amplification. The enzyme is ready-to-load. No extra dye or loading buffer is needed!
m-Superhot Taq DNA pol.
M-Superhot Taq Polymerase is developed to enhance the specificity, sensitivity and yield of DNA amplification. The enzyme provides a convenient setting up at room temperature
m-Anti-Taq
Mouse Monoclonal Antibody - Enhancer for Polymerase reactions
p-Superhot Taq DNA pol.
p-Superhot Taq Polymerase is developed to enhance the specificity and yield of DNA amplification. The polymerase provides a convenient setting up at room temperature because of blocking the the enzyme with optimized mix of inhibitors
Pfu/Psp DNA Polymerase
Pfu DNA polymerase generated PCR fragments exhibits the lowest error rate of any thermostable DNA polymerases. The fragments are blunt-ended for direct ligation
Pfu/Psp red DNA Polymerase RTL
Pfu DNA polymerase (RTU=READY-TO-LOAD) is a convenient Mixture of proof-reading Enzyme, red dye and loading buffer. It generated PCR fragments exhibits the lowest error rate of any thermostable DNA polymerases. The fragements are blunt-ended for direct ligation
Pfu/Psp DNA Polymerase 2X-preMix
Pfu DNA polymerase 2X-preMix is a convenient Mixture of proof-reading Enzyme, reaction buffer dNTP´s and MgCl2. It generated PCR fragments exhibits the lowest error rate of any thermostable DNA polymerases. The fragements are blunt-ended for direct ligation
Tth DNA Polymerase
Tth DNA Polymerase Maximo is used to reverse-transcribe RNA efficiently in the presence of manganese. PCR can be performed in the same tube using the intrinsic DNA polymerase activity simply by chelation of manganese cation and the addition of magnesium.



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