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Model Number |
K0561003 |
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Taq for General PCR applications
- Ultrapure, thermostable recombinant enzyme purified from the cloned Thermus
aquaticus DNA Polymerase gene expressed in E.coli
- Composition of all optimized reagents for PCR reaction (Taq polymerase, Taq buffer,
dNTP mix, loading dye and enhancer) in a kit
- One unit is the amount of enzyme required to catalyze the incorporation of 10nmoles
of nucleotides into acid-insoluble material in 30 minutes at 74�
- A supply of enhancer, Magic buffer for GC rich template
- Flexible choice either Taq with reaction buffer containing MgCl2or Taq with MgCl2 free
reaction buffer and separate MgCl2
- Concentration: 5 units/ul
- 5'->3' exonuclease activity
- Amplification efficiency: ≥10 fold
- No Nuclease, RNase, Protease contamination
- Amplification range:
- lambda DNA : up to 6Kb (Max. 12Kb)
- human genomic DNA : up to 2Kb (Max. 4Kb)
- Stable at -20�
- Applications
- Amplification of genomic DNA and cDAN targets up to 3Kb long
- GC-rich sequences or secondary structures
- TA Cloning
- RT-PCR
- Different Display
- Mulitplex PCR
- Degenerate PCR
- PCR-based DNA fingerprinting (VNTR, STR and RAPD) etc.
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Label |
Content & Use |
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Taq DNA Polymerase |
[5U/ul] in storage buffer 20mM Tris-Cl (pH 8.0),
100mM KCl, 0.1mM EDTA, 1mM DTT
0.5% Tween 20, 0.5% Nonidet P-40, 50% Glycerol |
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10X Taq buffer I (w/MgCl2) |
100mM Tris-HCl (pH 8.3), 500mM KCl, 20mM MgCl2 |
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10X Taq buffer II (w/o MgCl2) |
100mM Tris-HCl (pH 8.3), 500mM KCl |
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MgCl2 Stock Solution |
MgCl2 |
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10X dNTP mix |
2.5mM(each) dATP, dTTP, dGTP, dCTP |
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4X Magic Buffer |
For amplification of GC rich template |
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10X Loading Dye |
For gel loading |
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dH2O |
DNase free water | |
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Enzyme activity
PCR for 1ng of lambda(A) and E.coli(B) was performed using dilution series
of 5 different Taq DNA Polymerase with 1X, 1/5, 1/10, 1/50, and 1/100.
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Lane 1 & 6 : 5U
Lane 3 & 8 : 0.5U
Lane 5 & 10 : 0.05U |
Lane 2 & 7 : 1U
Lane 4 & 9 : 0.1U
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Sensitivity for GC rich contents
The Magic buffer is very useful to amplify high GC contents or complicated
structure of DNA. Human genomic DNA was amplified from 10ng to 3Kb by adding Magic buffer (0.5~2x) to 1U of Taq DNA Polymerase.
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Lane 1 : lambda/Hind III
Lane 2 : 2x Magic Buffer
Lane 3 : 1x Magic Buffer |
Lane 4 : 0.5x Magic Buffer
Lane 5 : No Magic Buffer
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No DNA contamination is shown in lane 4.
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Lane 1 : DW
Lane 2 : Taq A
Lane 3 : Taq B
Lane 4 : KOMA Taq
Lane 5 : Taq C
Lane 6 : Taq D
Lane 7 : Taq E |
Lane 8 : Taq F
Lane 9 : 1pg E.coli DNA
Lane 10 : 100fg E.coli DNA
Lane 11 : 10fg E.coli DNA
Lane 12 : 1fg E.coli DNA
Lane 13 : 100bp ladder
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* Lane 1 : Negative control
* Lane 2-8 : Other vendor's Taq polymerase (No template)
* Lane 9-12 : Positive control | | |
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Cat. No. |
Product |
Size |
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K0561001 |
Taq DNA Polymerase |
250U |
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K0561002 |
Taq DNA Polymerase |
500U |
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K0561003 |
Taq DNA Polymerase |
1000U |
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K0561004 |
Taq DNA Polymerase (MgCl2 Free Reaction Buffer) |
250U |
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K0561005 |
Taq DNA Polymerase (MgCl2 Free Reaction Buffer) |
500U |
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K0561006 |
Taq DNA Polymerase (MgCl2 Free Reaction Buffer) |
1000U | |
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