
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.
ZNF32 (zinc finger protein 32) encodes a zinc finger protein that enables sequence-specific binding to double-stranded DNA. It is predicted to function in the regulation of transcription by RNA polymerase II and is primarily associated with the nucleus. Its DNA-binding activity suggests a role in transcriptional regulation and chromatin-associated processes, making ZNF32 relevant for studying mechanisms that control gene expression and transcriptional 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.
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 3
Reference Transcript: NM_006973
Frameshift Mutation Strategy
For research use only. Not intended for human or animal clinical trials, therapeutic or diagnostic use





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