TaqFast DNA Polymerase Store at -20°C
Product Description TaqFast DNA polymerase is an engineered version of Taq DNA polymerase developed
to achieve rapid PCR. It catalyzes the 5’-3’ synthesis of DNA. This enzyme possesses
5’-3’ exonuclease activity and moderate 3’-5’ proofreading exonuclease activity. The
extension speed is about 6 kb/min, which is 6 times faster than the regular Taq DNA
polymerase. Template-independent “A” can be attached at the 3’ end of the PCR
product which can then be cloned into a TA cloning vector.
| Product Components | 250U | 1000U |
| TaqFast DNA Polymerase (5 U/µl) | 50 µl | 200 µl |
| 5X PCR Buffer, with Mg2+ | 1 ml | 4 ml |
| 25 mM MgSO4 | 1 ml | 1 ml |
Storage Buffer Components 50 mM Tris-HCl (pH 8.0), 100 mM NaCl, 0.1 mM EDTA, 5 mM DTT, 50 % glycerol and 1.0 %
Triton®X-100.
Unit Definition One unit of the enzyme catalyzes the incorporation of 10 nmol of deoxyribonucleotides
into a polynucleotide fraction in 30 mins at 74°C.
Shipping and Storage Upon arrival, TaqFast DNA Polymerase should be stored at -20°C. Avoid repeated
freeze-thaw cycles of all TaqFast components to retain maximum performance. All
TaqFast components are stable for 1 year from the date of shipping if stored and
handled properly.
Protocol The following basic protocol serves as a general guideline and starting point for any
PCR amplification. Optimal reaction conditions (incubation times, temperatures,
concentration of Taq DNA Polymerase, primers, MgSO4 and template DNA) may vary
and need to be optimized for each specific PCR.
All PCR experiments should be assembled in a nuclease-free environment. In addition,
DNA sample preparation, reaction set-up and subsequent reaction(s) should be
performed in separate areas to avoid cross contamination.
A negative control reaction (omitting template DNA) should always be performed in
tandem with sample PCR to confirm the absence of DNA contamination.
1. Add the following components to a sterile 0.2 ml PCR tube sitting on ice.
| Components | Volume | Final Concentration |
| Template DNA | 100 ng | 2 ng/µl |
| Forward primer (10 µM) | 1 - 2.5 µl | 200 - 500 nM |
| Reverse primer (10 µM) | 1 - 2.5 µl | 200 - 500 nM |
| 5X PCR Buffer, with Mg2+ | 10 µl | 1X |
| 25 mM MgSO4 (optional)* | 0 - 3 µl | 1.5 - 3 mM |
| dNTP Mix (10 mM) | 1 µl | 200 µM |
| TaqFast DNA Polymerase (5 U/µl) | 0.5 - 1 µl | 2.5 - 5 U |
| Nuclease-Free H2O | up to 50 µl | - |
* Optimal Mg2+ concentration is specific to each DNA template-primer set and
can only be determined experimentally.
• We recommend preparing a mastermix for multiple reactions to minimize
reagent loss and enable accurate pipetting.
2. Mix contents of tube and centrifuge briefly.
3. Incubate tube in a thermal cycler at 94°C for 3 mins to completely denature the
template.
4. Perform 30 - 35 cycles of PCR amplification as follows:
Denature: 94°C for 5 sec
Anneal: 45 - 72°C for 15 sec
Extend: 72°C for 10 sec/1 kb template
5. Incubate for an additional 5 mins at 72°C and maintain the reaction at 4°C. The
samples can be stored at -20°C until use.
6. Analyze the amplification products by agarose gel electrophoresis and visualize
by ethidium bromide or SafeView™ (Cat No. G108) staining. Use appropriate
molecular weight standards.
