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- AbTaq 2.0 Polymerase
AbTaq 2.0 Polymerase
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Product Description
AbTaq 2.0 Polymerase is a Taq DNA polymerase enzyme engineered for fast extension speeds, thermal stability and a hot start function. AbTaq Polymerase is tolerant of common PCR inhibitors such as whole blood and is suitable for TaqMan assays.
Catalog Number | Component Name | Size/Amount | Concentration |
---|---|---|---|
OP-TP-001-200U | |||
AbTaq 2.0 Polymerase | 200U / 1 x 40uL | 5U/uL | |
10x AbTaq Buffer | 1 x 1.25mL | 10x | |
OP-TP-001-1000U | |||
AbTaq 2.0 Polymerase | 1000U / 1 x 200uL | 5U/uL | |
10x AbTaq Buffer | 1 x 5mL | 10x | |
OP-TP-001-2500U | |||
AbTaq 2.0 Polymerase | 2500U / 1 x 500uL | 5U/uL | |
10x AbTaq Buffer | 1 x 7mL | 10x | |
OP-TP-001-1000U-GF | |||
AbTaq 2.0 Polymerase | 1000U / 1 x 200uL | 5U/uL | |
10x AbTaq Buffer | 1 x 5mL | 10x |
Features | Specifications |
---|---|
Concentration | 5U/uL |
Recombinant Enzyme | Yes |
Enzyme Activity | 5’ ->3’ exonuclease activity |
Sample/Target | Genomic DNA, plasmid and cDNA |
With Hotstart | Yes |
dNTPs included | No |
Reaction Condition | At 1x concentration the reaction buffer assures optimal activity for AbTaq 2.0 Polymerase |
Unit Assay
The unit concentration of each lot has been determined to be at least 5U/uL
RNase-Free
Each lot shows no detectable degradation of RNA when 5U of enzyme and 1x concentration of buffer was incubated with 500ng of RNA ladder for 1 hour at 37℃ as determined by agarose gel electrophoresis.
Protein Purity
Each lot is ≥90% pure as determined by SDS-PAGE analysis using Coomassie blue detection