Recombinant Streptococcus aureus tag-free Cas9 nuclease expressed in an Escherichia coli with both N-terminal and C-terminal nucleic localization signal (NLS).
Host:
Escherichia coli
Theoretical MW (kDa):
~130 kDa
Form:
Liquid
Preparation Method:
Escherichia coli expression system
Purity:
≥ 95% as analyzed by SDS-PAGE ≥ 90% as analyzed by SEC-HPLC
Endotoxin Level:
≤ 10 EU/mg as analyzed by gel clotting method
Quality Control Testing:
Cleavage assay
A 20 uL reaction in 1xSaCas9 Nuclease Reaction Buffer containing linearized plasmid, gRNA, and SaCas9 2NLS Nuclease for 2 hours at 37°C results in a digestion efficiency of linearized plasmid higher than 90%, as determined by agarose gel electrophoresis.
Recommend Usage:
CRISPR Genomic editing The optimal working dilution should be determined by the end user.
Storage Buffer:
In 20 mM Tris, 300 mM NaCl, 0.1 mM TCEP, pH7.5 (50% glycerol).
Storage Instruction:
Store at -20°C. Aliquot to avoid repeated freezing and thawing.