
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.
ZNF875 (zinc finger protein 875) encodes a zinc finger protein with predicted sequence-specific DNA-binding activity and predicted transcription factor function. It is predicted to regulate RNA polymerase II-dependent transcription through interactions with transcriptional regulatory regions and is predicted to function in the nucleus. The specific molecular targets and biological processes controlled by ZNF875 remain incompletely characterized.
A human gastric carcinoma cell line established from a metastatic lymph node. It was originally derived from gastric cancer and described as an undifferentiated, mucin-producing tumor cell line.
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.
For research use only. Not intended for human or animal clinical trials, therapeutic or diagnostic use





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