
CRISPR knockout cell lines are engineered through targeted genome editing to eliminate gene function, supporting studies of cellular biology, disease mechanisms, and drug discovery.
ZNF142 (zinc finger protein 142) encodes a Kruppel family C2H2-type zinc finger protein containing multiple zinc finger domains. The protein may function in transcriptional regulation through sequence-specific DNA binding and regulatory interactions. Its extensive zinc finger domain architecture supports a role in control of gene expression and makes ZNF142 relevant to studies of transcriptional regulation and cellular phenotype.
AGS is a human gastric adenocarcinoma cell line established from a primary stomach tumor of a 54-year-old female patient who had not received prior anticancer treatment. The cells are derived from gastric adenocarcinoma and are used as a model for studying gastric cancer biology, tumor-related signaling pathways, infection-related mechanisms, and therapeutic responses. AGS cells have been reported to carry persistent parainfluenza virus type 5 (PIV5) infection.
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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