
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.
ZDHHC12 (zDHHC palmitoyltransferase 12) encodes a protein-cysteine S-palmitoyltransferase involved in protein palmitoylation. The protein localizes primarily to the Golgi apparatus and endoplasmic reticulum and contributes to gephyrin clustering associated with postsynaptic density assembly. ZDHHC12 also participates in negative regulation of NLRP3 inflammasome complex assembly, linking protein lipid modification with neuronal and inflammatory cellular processes.
A human colon carcinoma cell line developed by Michael Brattain. The cells are derived from colon tissue and are classified as a cancer cell line.
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_032799
Frameshift Mutation Strategy
For research use only. Not intended for human or animal clinical trials, therapeutic or diagnostic use





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