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NZYTaq II DNA polymerase
NZYTaq II DNA polymerase belongs to a new generation of Taq-derived DNA polymerases optimized for standard PCR applications. The enzyme was engineered to produce high DNA yields in shorter PCR running times (15-30 s/kb extension) under minimal optimization conditions.
NZYTaq II DNA polymerase belongs to a new generation of Taq-derived DNA polymerases optimized for standard PCR applications. The enzyme was engineered to produce high DNA yields in shorter PCR running times (15-30 s/kb extension) under minimal optimization conditions. NZYTaq II DNA polymerase lacks 3'→5' exonuclease activity and supports the robust and reliable amplification of a wide range of DNA templates up to 6 kb. The enzyme was optimized to provide higher sensitivity, allowing amplification of different DNA fragments from as little as 5 pg of human genomic DNA. Resulting PCR products have an A-overhang and are suitable for cloning with NZYtech's TA PCR cloning kits (MB053 or MB137).
Extension time: 15-30 sec/kb at 72 °C
3'→5' activity: no
Product overhang: 3'-A
Extension time: 15-30 sec/kb at 72 °C
3'→5' activity: no
Product overhang: 3'-A
| Shipping Conditions | Room Temperature |
|---|---|
| Storage Conditions | -85°C to -15°C |
| Application | Routine PCR, TA Cloning |
| Features | Standard |
| Product Length | 0-6 kb |
| Format | Enzyme/Protein |
| Product Category | End-Point PCR |
| Concentration | 5 U/μL |
| Hot Start | No |
– NZYTaq II DNA polymerase (5 U/μL)
– Reaction buffer (10x)
– MgCl2 Solution (50 mM)
– Reaction buffer (10x)
– MgCl2 Solution (50 mM)
| Shipping Conditions | Room Temperature |
|---|---|
| Storage Conditions | -85°C to -15°C |
| Application | Routine PCR, TA Cloning |
| Features | Standard |
| Product Length | 0-6 kb |
| Format | Enzyme/Protein |
| Product Category | End-Point PCR |
| Concentration | 5 U/μL |
| Hot Start | No |
C14ORF39/SIX6OS1 is a constituent of the synaptonemal complex and is essential for mouse fertility
Gómez-H L, Felipe-Medina N, Sánchez-Martín M, Davies OR, Ramos I, García-Tuñón I, de Rooij DG, Dereli I, Tóth A, Barbero JL, Benavente R, Llano E, Pendas AM.
Nature Communications, 2016
Mitochondrial DNA D-loop amplification and sequencing for species differentiation in milk.
Baptista M, Domingues L.
Methods in Molecular Biology, 2024
| Shipping Conditions | Room Temperature |
|---|---|
| Storage Conditions | -85°C to -15°C |
| Application | Routine PCR, TA Cloning |
| Features | Standard |
| Product Length | 0-6 kb |
| Format | Enzyme/Protein |
| Product Category | End-Point PCR |
| Concentration | 5 U/μL |
| Hot Start | No |
| Shipping Conditions | Room Temperature |
|---|---|
| Storage Conditions | -85°C to -15°C |
| Application | Routine PCR, TA Cloning |
| Features | Standard |
| Product Length | 0-6 kb |
| Format | Enzyme/Protein |
| Product Category | End-Point PCR |
| Concentration | 5 U/μL |
| Hot Start | No |
| Shipping Conditions | Room Temperature |
|---|---|
| Storage Conditions | -85°C to -15°C |
| Application | Routine PCR, TA Cloning |
| Features | Standard |
| Product Length | 0-6 kb |
| Format | Enzyme/Protein |
| Product Category | End-Point PCR |
| Concentration | 5 U/μL |
| Hot Start | No |
CoA
Certificate of Analysis
