
CRISPR knockout cell lines are engineered through targeted genome editing to eliminate gene function, supporting studies of cellular biology, disease mechanisms, and drug discovery.
ASNS (asparagine synthetase [glutamine-hydrolyzing]) encodes an enzyme that catalyzes the synthesis of asparagine from glutamine and other metabolic substrates. Asparagine synthetase supports cellular amino acid metabolism and contributes to maintaining intracellular asparagine availability. Its activity is also associated with cell proliferation, reflecting the importance of asparagine biosynthesis for cellular growth and metabolism.
A human esophageal cancer cell line established from a poorly differentiated squamous cell carcinoma of the upper cervical esophagus in a 49-year-old woman after radiotherapy. KYSE-150 carries amplified c-erb-B and cyclin D1 oncogenes and has been reported to produce tumors in nude mice. The cell line has been extensively characterized and is included in large-scale cancer cell line resources.
Each knockout cell line is validated by STR authentication, sterility testing (bacteria/fungi), and mycoplasma screening. Genotype is confirmed by two rounds of PCR and Sanger sequencing. Only clones that pass all QC criteria are released, ensuring reliable identity and performance for downstream applications.

Cas9 cell lines in our cell bank can stably express Cas9 protein. Each Cas9 Stable Cell Line is easy to use and enables gene knockout simply by transfecting gRNA, while transfection of gRNA and donor DNA results in gene knock-in or point mutations
These Cas9 stable cell lines have been used to construct the KO cell lines for various genes, gene KO efficiency 5-10 times improved.
Selected cells, low passages, good cell condition, high activity, applicable for all kinds of gene-editing experiments.
For research use only. Not intended for human or animal clinical trials, therapeutic or diagnostic use





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