
CRISPR knockout cell lines are engineered through targeted genome editing to eliminate gene function, supporting studies of cellular biology, disease mechanisms, and drug discovery.
ZNF317 (zinc finger protein 317) encodes a zinc finger-containing transcription factor predicted to bind DNA in a sequence-specific manner. It is associated with regulation of transcription by RNA polymerase II and is localized to the nucleus. ZNF317 is therefore relevant to studies of transcriptional regulation, gene expression, and mechanisms controlling RNA polymerase II-dependent transcription.
A human gastric tubular adenocarcinoma cell line established from a nude mouse xenograft of metastatic liver tissue. The cells were derived from a male donor and are classified as a gastric cancer cell line.
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.

Targeted knockout region: EExon 3
Reference Transcript: NM_020933
Frameshift Mutation Strategy
For research use only. Not intended for human or animal clinical trials, therapeutic or diagnostic use





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