T7 Endonuclease I (from Escherichia coli), Intact Genomics
Supplier: InstruCon, Inc.Total Ratings: 0
Avg. Ratings: 0.0 out of 5
T7 endonuclease I is useful for quantitatively estimating the nuclease-induced mutation frequency of gene edited cells and other applications.
- Extremely high purity
- Useful to resolve four-way junction or branched DNA, detect/cleave heteroduplex/nicked DNA, and randomly cleave linear DNA for shot-gun cloning
- Quality control is performed following the production of each new lot of product to ensure that it meets the quality standards and specifications designated for the product
- 10X T7 endonuclease I reaction buffer
T7 endonuclease I, a stable homodimer of identical 149 amino acid subunits is the product of a recombinant gene in E. coli. Double-stranded breaks (DSBs) generated by CRISPR/TALEN at desired target sites can be PCR-amplified, and the PCR products can be denatured and re-annealed to form mismatched DNA. If the mismatched DNA length position is more than 1 bp, T7 endonuclease I can recognize and cleave it. It is useful for quantitatively estimating the nuclease-induced mutation frequency of gene edited cells.
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