Cat. No. : BN0190-0250
units : 250 U
Concentration : 5 units/μl
Volume : 50 μl
Storage : -20 ℃ |
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Supplied form |
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20mM Tris-HCl pH8.0, 50%glycerol,
100mM KCl, 0.1Mm EDTA, 1mM DTT,
0.5%Tween20, 0.5%NP-40 |
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Description |
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VAS Taq is isolated and purified from an
E.Coli. strain that carries the cloned DNA
polymerase gene from Thermus aquqticus
YT-1strain.An inert blue dye is added. |
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Purity(SDS-PAGE)>99% |
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10X VAS Taq PCR Buffer |
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Volume: 1ml / vial
Composition: Tris-HCl, KCl, (NH4)2SO4,
15mM MgCl2, pH8.3 . |
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Unit definition |
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One unit is the amount of enzyme that
will incorporate 10 nmoles of dNTPs into
acid-insoluble products at 72 in 30 ℃ min. |
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Primer-mix |
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Hexamers primer-mix for random annealing at 30°C |
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PCR performance test |
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Good performance of DNA amplification
by PCR is confirmed by using 2 U Taq will
amplified 2.5 kb DNA fragment in a 50μl
reaction volume. |
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General reaction mixture for PCR
( total 50μl ) |
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Taq (5 units/μl ) |
0.5μl |
10X Taq Buffer |
5μl |
dNTPs(2.5mM) |
4μl |
Template |
< 1μg |
Primer 1 |
0.2~1.0μM |
Primer 2 |
0.2~1.0μM |
H2O |
upto 50μl |
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PCR products |
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As most PCR product amplified with
VAS Taq have one A added at
3`- terminus, the obtained PCR product can
be directly used for cloning into T-vector. |
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