
CRISPR knockout cell lines are engineered through targeted genome editing to eliminate gene function, supporting studies of cellular biology, disease mechanisms, and drug discovery.
ZNF367 (zinc finger protein 367) encodes a zinc finger-containing transcription factor with predicted DNA-binding activity. ZNF367 is localized to the nucleoplasm and is predicted to regulate RNA polymerase II-dependent transcription. Through sequence-specific DNA binding, it may contribute to transcriptional control of cellular genes, although its specific target genes and biological pathways remain incompletely characterized.
A human urinary bladder transitional papillary tumor cell line established in 1968 from a recurrent, well-differentiated papillary tumor of a 63-year-old man. The original tumor was classified as clinical stage T2 and histological grade G1 and had been treated previously with gold grains and subsequently with diathermy following recurrence.
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 1
Reference Transcript: NM_153695
Frameshift Mutation Strategy
For research use only. Not intended for human or animal clinical trials, therapeutic or diagnostic use





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