Cat. No. : BN0190-0250
units : 250 U
Concentration : 5 units/μl
Volume : 50 μl
Storage : -20 ℃ |
| |
| Supplied form |
| |
20mM Tris-HCl pH8.0, 50%glycerol,
100mM KCl, 0.1Mm EDTA, 1mM DTT,
0.5%Tween20, 0.5%NP-40 |
| |
|
| Description |
| |
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. |
| |
|
| Purity(SDS-PAGE)>99% |
| |
|
| 10X VAS Taq PCR Buffer |
| |
Volume: 1ml / vial
Composition: Tris-HCl, KCl, (NH4)2SO4,
15mM MgCl2, pH8.3 . |
| |
|
| Unit definition |
| |
One unit is the amount of enzyme that
will incorporate 10 nmoles of dNTPs into
acid-insoluble products at 72 in 30 ℃ min. |
| |
|
| Primer-mix |
| |
Hexamers primer-mix for random annealing at 30°C |
| |
|
| PCR performance test |
| |
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. |
| |
|
| General reaction mixture for PCR
( total 50μl ) |
| |
| 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 |
|
| |
|
| PCR products |
| |
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. |
| |
|
| |
|