
CRISPR knockout cell lines are engineered through targeted genome editing to eliminate gene function, supporting studies of cellular biology, disease mechanisms, and drug discovery.
ZNHIT1 (zinc finger HIT-type containing 1) encodes a nuclear protein with histone-binding activity. It is involved in muscle cell differentiation and contributes to positive regulation of DNA damage responses mediated by p53-class signaling. Through its interactions with histones and participation in cellular response pathways, ZNHIT1 may contribute to coordination of chromatin-associated regulation, differentiation, and genome damage responses.
NCI-H1975 is a human non-small cell lung cancer cell line established from lung tumor tissue. The donor was a non-smoker. The cell line is used as a model for studying lung cancer biology and molecular mechanisms associated with non-small cell lung carcinoma.
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 2
Reference Transcript: NM_006349
Frameshift Mutation Strategy
For research use only. Not intended for human or animal clinical trials, therapeutic or diagnostic use





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