
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.
ZDHHC11B (zDHHC palmitoyltransferase 11B, putative) encodes a protein predicted to possess protein-cysteine S-palmitoyltransferase activity. It is predicted to participate in protein palmitoylation and antiviral innate immune responses and to promote host defense against viral infection. ZDHHC11B is predicted to localize to endosomal membranes and to function in the Golgi apparatus and endoplasmic reticulum, suggesting a role in membrane-associated regulation of protein signaling and trafficking.
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_173798
Frameshift Mutation Strategy
For research use only. Not intended for human or animal clinical trials, therapeutic or diagnostic use





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