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Highlights
- High fidelity, hot-start NGS polymerase with minimal GC-bias across diverse templates.
- Strong fluorescent signal for real-time quantification and auto-normalization of libraries in iconPCR® workflows.
- Rapid reaction setup: just add water, primers, and template.
Original Manufacturer
100% satisfaction guaranteed, read Our Promise
Innovated in California, Made in the USA
Highlights
- High fidelity, hot-start NGS polymerase with minimal GC-bias across diverse templates.
- Strong fluorescent signal for real-time quantification and auto-normalization of libraries in iconPCR® workflows.
- Rapid reaction setup: just add water, primers, and template.
Original Manufacturer
100% satisfaction guaranteed, read Our Promise
Innovated in California, Made in the USA
Description
Performance
Technical Specifications
| Activity: | The polymerase contains both 5'-3' polymerization and 3'-5' proofreading activity. Both activities are inhibited prior to initialization. |
|---|---|
| Concentration: | 2X |
| Storage: | Store at ≤ -20°C for up to 12 months. Minimize exposure to light. Avoid repeated freeze/thawing of reagents. |
| Equipment: | Real-time PCR can be performed on any instrument that has optical scanners that do not require a passive reference dye. Instruments that individually modulate sample cycling via fluorescence (e.g. iconPCR®) can produce auto-normalized products. |
Resources
Documents
FAQ
The PolStarTM NGS Library Prep qPCR Premix can accommodate an amplicon length of 2kb with the cycling conditions provided in the protocol. Robust amplification of templates up to or exceeding 10kb can be achieved but may require empirical determination of cycling conditions for optimal results.
When combined with qPCR instruments that control PCR cycles of individual samples based on fluorescence (e.g. iconPCR®), the PolStarTM Premix can produce auto-normalized libraries while enabling real-time QC during library amplification.
2.2-3.6x10-6 errors/bp incorporated.
Yes. Both the polymerization and proofreading activities of the polymerase are strongly inhibited prior to heat-activation.
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