
CRISPR knockout cell lines are engineered through targeted genome editing to eliminate gene function, supporting studies of cellular biology, disease mechanisms, and drug discovery.
ARID1A (AT-rich interaction domain 1A) encodes a subunit of the SWI/SNF family of ATP-dependent chromatin remodeling complexes. ARID1A contributes to regulation of gene transcription by altering chromatin structure and accessibility and may help confer target specificity to the remodeling complex through DNA and protein interactions. It therefore plays an important role in chromatin-mediated control of gene expression.
Human high-grade ovarian serous adenocarcinoma cells derived in situ from the ovary are represented by HEY. The female-derived line is microsatellite stable and carries homozygous BRAF p.Gly464Glu and heterozygous KRAS p.Gly12Asp mutations.
Comprehensive quality control includes STR authentication, sterility testing (bacteria and fungi), and mycoplasma screening to ensure purity and performance. Genotype is confirmed by two rounds of PCR and Sanger sequencing, and complete validation reports are provided for make-to-order products.

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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