
CRISPR knockout cell lines are engineered through targeted genome editing to eliminate gene function, supporting studies of cellular biology, disease mechanisms, and drug discovery.
ZNF300 (zinc finger protein 300) encodes a C2H2-type zinc finger protein that is predicted to function as a DNA-binding transcriptional regulator. Although its molecular function has not been established, the presence of zinc finger domains suggests a potential role in transcriptional regulation. The biological targets, regulatory mechanisms, and cellular processes controlled by ZNF300 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.

Targeted knockout region: EExon 7
Reference Transcript: NM_001172831
Frameshift Mutation Strategy
For research use only. Not intended for human or animal clinical trials, therapeutic or diagnostic use





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