
CRISPR knockout cell lines are engineered through targeted genome editing to eliminate gene function, supporting studies of cellular biology, disease mechanisms, and drug discovery.
ZDHHC9 (zDHHC palmitoyltransferase 9) encodes an integral membrane palmitoyltransferase belonging to the zinc finger DHHC-domain family. The protein forms a complex with GOLGA7 and catalyzes palmitoylation of Ras family proteins including HRAS and NRAS. ZDHHC9 is relevant to studies of protein lipid modification, membrane-associated signaling, and regulation of Ras protein activity.
The Caki-1 cell line was established in 1971 from a cutaneous metastasis of a kidney adenocarcinoma in a 49-year-old male patient. It is a human renal carcinoma cell line used as an in vitro model for studying kidney cancer biology and related molecular mechanisms.
Each knockout cell line is validated by STR authentication, sterility testing (bacteria/fungi), and mycoplasma screening. Genotype is confirmed by two rounds of PCR and Sanger sequencing. Only clones that pass all QC criteria are released, ensuring reliable identity and performance for downstream applications.

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 3
Reference Transcript: NM_016032
Frameshift Mutation Strategy
For research use only. Not intended for human or animal clinical trials, therapeutic or diagnostic use






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