| Taq Premix with Dye |
25 ul |
| Template |
< 500 ng |
| Primer 1 |
0.2~1.0 uM (final conc.) |
| Primer 2 |
0.2~1.0 uM (final conc.) |
| Sterile Distilled Water |
up to 50 ul |
Concentration
One unit is defined as the amount of enzyme that can incorporate 10nmols of total dNTPs into an acid-insoluble material in 30 minutes at 74℃ when activated salmon sperm DNA was used as template / primer.
Quality Assurance
Greater than 95% purity as determined by SDS-PAGE (CBBstaining). The absence of endonuclease and exonucleases was confirmed.
PCR Product
PCR products have one A added at the 3'-terminus. Thus, the PCR product can be used directly for cloning into a T-vector. Additionally, it is possible to clone the product in blunt-end vectors after blunting and phosphorylation of the end.
PCR Test
Good amplification result was obtained in PCR reaction using λDNA as a template (Fig.1).
PCR condition
98℃ 10 sec
57℃ 30 sec
72℃ 8 min 25 cycles (2 min in the case of 2kb DNA)
Premix Composition
10 mM Tris-HCl, 50 mM MgCl2, 0.2 mM dNTPs, 5 % Glycerol, 0.08 % NP-40, 0.05 % Tween-20, 25 units/ml Taq DNA Polymerase, pH 8.6 @ 25℃
Storage
- 20℃ , Notes: Repeated freezing and thawing may decrease enzyme activity. Once thawed, aliquot into PCR tubes and store at -20℃. If you store this product at 4℃, please use it within 3 months.