
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.
AADAT (aminoadipate aminotransferase) encodes a mitochondrial aminotransferase involved in amino acid metabolism. The enzyme catalyzes transamination of alpha-aminoadipic acid, a step in the saccharopine pathway of L-lysine catabolism, and also catalyzes conversion of kynurenine to kynurenic acid, a metabolite with neuroactive properties. Through these activities, AADAT contributes to lysine and tryptophan metabolism and may influence cellular levels of metabolites involved in metabolic and neuronal processes.
A human gastric tubular adenocarcinoma cell line established from a nude mouse xenograft of metastatic liver tissue. The cells were derived from a male donor and are classified as a gastric cancer 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 3
Reference Transcript: NM_001286683
Frameshift Mutation Strategy
For research use only. Not intended for human or animal clinical trials, therapeutic or diagnostic use






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