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Format
ZymoTaq qPCR Premix
Highlights
- Hot-start polymerase for easy setup at room temperature.
- Robust amplification of DNA for genotyping, SNP, and HRM analysis.
- Strong fluorescent signal for real-time and quantitative PCR assays.

Original Manufacturer
Innovated in California, Made in the USA
Satisfaction 100% guaranteed, read Our Promise
Format
ZymoTaq qPCR Premix
Highlights
- Hot-start polymerase for easy setup at room temperature.
- Robust amplification of DNA for genotyping, SNP, and HRM analysis.
- Strong fluorescent signal for real-time and quantitative PCR assays.
-
Enzyme (5 U/µl)
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Best Seller
PreMix
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qPCR Premix

Original Manufacturer
Innovated in California, Made in the USA
Satisfaction 100% guaranteed, read Our Promise
Cat # | Name | Size | Price | Quantity |
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Cat # | Name | Size | Price | |
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W1001-1 | DNase/RNase-Free Water | 1 ml | $11.60 | |
Description
Performance
Technical Specifications
Activity | 5' - 3' DNA polymerization |
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Concentration | Reaction conditions at 1X (50 µl total volume) will contain 2 U of ZymoTaq DNA polymerase. |
Equipment | Real-time PCR can be performed on any instrument that has optical scanners that do not require passive reference dye. |
Storage | Store at ≤ -20°C for up to 12 months. Minimize exposure to light. Avoid repeated freeze/thawing of reagents. |
Unit Definition | One unit (U) enzyme of ZymoTaq DNA Polymerase is defined as the amount of enzyme required for the incorporation of 10 nmol dNTPs into an acid-insoluble form in 30 minutes at 72°C. |
Resources
Documents
FAQ
The error rate for ZymoTaq DNA polymerase ranges from 1.1x10-4 to 8.9x10-5.
The ZymoTaq DNA polymerase can amplify up to 5 kb.
The ZymoTaq DNA PCR system utilizes a hot-start polymerase and is optimized for bisulfite PCR and other GC rich templates, as well as low-copy number of DNA templates. It can also be used for general molecular biology applications as well (e.g. suitable for TA cloning, multiplex PCR, etc).
Yes.
Citations
The ZymoTaq PreMix was specifically used to amplify bisulfite-treated DNA with no reports of inefficient or nonspecific amplification in a study of dynamic DNA methylation expression levels during different development stages. Results showed that timing of variations in methylation patterns were specific for genes related to growth.
Fang X, et. al. (2013) Global and gene specific DNA methylation changes during zebrafish development. Comp Biochem Physiol B Biochem Mol Biol. 166(1):99-108.Need help? Contact Us