
Gene knockout cell lines are generated using CRISPR-Cas9 based technology to precisely disrupt target genes, enabling functional genomics research, disease modeling, and target validation.
ZNF211 (zinc finger protein 211) encodes a zinc finger protein containing a Kruppel-associated box domain and multiple zinc finger domains. These structural features are consistent with potential roles in DNA binding and transcriptional regulation. ZNF211 may also participate in developmental processes, although its specific molecular mechanisms remain incompletely characterized.
AGS is a human gastric adenocarcinoma cell line established from a primary stomach tumor of a 54-year-old female patient who had not received prior anticancer treatment. The cells are derived from gastric adenocarcinoma and are used as a model for studying gastric cancer biology, tumor-related signaling pathways, infection-related mechanisms, and therapeutic responses. AGS cells have been reported to carry persistent parainfluenza virus type 5 (PIV5) infection.
Before delivery, each clone is authenticated by STR, tested for sterility and mycoplasma, and genotype‑verified by two‑round PCR‑sequencing. Comprehensive QC data accompany every shipment to support reproducible research.

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 5
Reference Transcript: NM_001265597
Frameshift Mutation Strategy
For research use only. Not intended for human or animal clinical trials, therapeutic or diagnostic use





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