
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.
ZSWIM8 (zinc finger SWIM-type containing 8) encodes a component of the Cul3-RING ubiquitin ligase complex that functions as a ubiquitin-like ligase-substrate adaptor. ZSWIM8 contributes to protein ubiquitination and proteolysis involved in protein catabolic processes. Through its role in ubiquitin-mediated regulation, ZSWIM8 participates in the control of macromolecule metabolism and cellular protein turnover.
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.
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 1
Reference Transcript: NM_015037
Frameshift Mutation Strategy
For research use only. Not intended for human or animal clinical trials, therapeutic or diagnostic use





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