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Invitrogen™ Platinum™ II Taq Hot-Start DNA Polymerase
Invitrogen Platinum II Taq Hot-Start DNA Polymerase is designed for universal primer annealing and fast, easy PCR with its unique combination of innovative buffer, high-performance engineered Taq DNA polymerase, and superior hot-start technology.
Brand: Invitrogen™
1680.08 EUR valid until 2024-12-14
Use promo code "21632" to get your promotional price.
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To receive the discount customers must purchase three of the same product at list price in a single order to receive 33.33% discount. There is no limit to the multiples of 3 that customers can buy. Use promo code ”21632” to get your promotional price
Includes: 1000 μL Platinum II Taq HS DNA Polymerase, 2x12.5 mL 5X Platinum II PCR Buffer, 2x12.5 mL Platinum GC Enhancer
Description
Invitrogen Platinum II Taq Hot-Start DNA Polymerase is designed for universal primer annealing and fast, easy PCR with its unique combination of innovative buffer, high-performance engineered Taq DNA polymerase, and superior hot-start technology.
Features of Platinum II Taq Hot-Start DNA Polymerase include:
- Innovative buffer—enables universal annealing temperature by isostabilizing primer-template duplex structures
- Engineered Taq DNA polymerase—confers fast cycling and resistance to common inhibitors
- Platinum hot-start technology—enables superior specificity, sensitivity, and yields; allows for room temperature reaction setup
Platinum II Taq Hot-Start DNA Polymerase is an engineered Taq DNA polymerase that shows increased resistance to reaction inhibitors originating from sample material or DNA purification steps. The polymerase has a higher DNA synthesis rate and delivers PCR results more than two times faster than other Taq DNA polymerases. Proprietary Platinum Taq antibodies block polymerase activity at ambient temperatures and dissociate after the initial denaturation step at 94°C. This automatic 'hot start' provides increased sensitivity, specificity, and yield, while allowing reaction assembly at room temperature.
Due to the unique composition of the Platinum II PCR buffer, the annealing temperature is 60°C for most primer pairs designed following the general design rules. Isostabilizing molecules in the buffer increase primer–template duplex stability during the annealing step and contribute to enhanced specificity without the need to optimize annealing temperature for each primer pair. With Platinum II Taq Hot-Start DNA Polymerase, different PCR assays can be cycled together using the same protocol with universal primer annealing temperature and the extension step selected for the longest fragment to be amplified.
Platinum II Taq Hot-Start DNA Polymerase is provided with the optional Platinum GC Enhancer for specific amplification and improved yields of GC-rich targets.
Use Platinum II Taq Hot-Start DNA Polymerase for the amplification of DNA from complex genomic, viral, and plasmid templates, as well as in RT-PCR, in applications like genotyping, high-throughput PCR, or with samples of suboptimal purity.
For increased convenience, we offer Platinum II Hot-Start PCR Master Mix (2X) (Cat. No. 14000012), where Platinum II Taq Hot-Start DNA Polymerase is provided in a ready-to-use mixture with Platinum II PCR buffer and dNTPs, thus reducing the number of pipetting steps during PCR reaction setup. Platinum II Hot-Start Green PCR Master Mix (2X) is also available, which additionally contains a density reagent and two tracking dyes for direct loading of PCR products on gels, further streamlining the PCR workflow from setup to final analysis of the result.
Specifications
• Platinum II Taq HS DNA Polymerase, 1000 μL • 5X Platinum II PCR Buffer, 2 x 12.5 mL • Platinum GC Enhancer, 2 x 12.5 mL Store at -20°C in a non-frost-free freezer. |
|
High | |
Fast or Standard | |
Dry Ice | |
2X | |
Built-In Hot Start | |
3'-A | |
5 kb or less |
Tube | |
Platinum II Taq Hot-Start DNA Polymerase | |
Hot Start DNA Polymerase | |
Hot-start PCR | |
1X | |
2500 Reactions | |
Separate Components | |
DNA |
For Research Use Only. Not for use in diagnostic procedures.