
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.
ZNF512 (zinc finger protein 512) encodes a protein containing four putative zinc finger motifs. Zinc finger domains can mediate interactions with proteins or nucleic acids, and proteins containing these motifs frequently participate in transcriptional regulation and other cellular processes. ZNF512 is therefore likely to function in molecular interactions involving nucleic acids or regulatory proteins, although its specific molecular targets and biological functions remain incompletely characterized.
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 6
Reference Transcript: NM_032434
Frameshift Mutation Strategy
For research use only. Not intended for human or animal clinical trials, therapeutic or diagnostic use





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