
CRISPR knockout cell lines are engineered through targeted genome editing to eliminate gene function, supporting studies of cellular biology, disease mechanisms, and drug discovery.
ZNF33A (zinc finger protein 33A) encodes a nuclear zinc finger protein predicted to function as a DNA-binding transcription factor involved in regulation of RNA polymerase II-dependent gene expression. The protein is predicted to recognize transcriptional regulatory regions and influence expression of target genes. Its specific DNA-binding sites, molecular partners, and biological functions remain incompletely characterized based on current annotation.
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 4
Reference Transcript: NM_001278170
Frameshift Mutation Strategy
For research use only. Not intended for human or animal clinical trials, therapeutic or diagnostic use





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