
Ubigene gene knockout cell lines mediated by optimized CRISPR-Cas9 technology provide reliable in vitro models for investigating gene function, signaling pathways, disease mechanisms, and therapeutic targets.
ZC3H12A (zinc finger CCCH-type containing 12A) encodes a CCCH-type zinc finger protein that has been described as an MCP1-induced transcriptional regulator. The protein has been implicated in activation of gene expression and induction of cardiomyocyte cell death, potentially through regulation of apoptosis-associated genes. Its biological activities suggest a role in transcriptional regulation and cellular survival, although the molecular mechanisms underlying these effects remain incompletely characterized.
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 2
Reference Transcript: NM_025079
Frameshift Mutation Strategy
For research use only. Not intended for human or animal clinical trials, therapeutic or diagnostic use





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