
CRISPR knockout cell lines are engineered through targeted genome editing to eliminate gene function, supporting studies of cellular biology, disease mechanisms, and drug discovery.
MTHFD1 (methylenetetrahydrofolate dehydrogenase, cyclohydrolase and formyltetrahydrofolate synthetase 1) encodes a trifunctional enzyme involved in folate-mediated one-carbon metabolism. It catalyzes three sequential reactions in the interconversion of tetrahydrofolate derivatives, providing substrates for methionine, thymidylate, and de novo purine synthesis. Its dehydrogenase and cyclohydrolase activities reside in an amino-terminal domain, while a separate, larger domain provides formyltetrahydrofolate synthetase activity.
A murine pancreatic ductal adenocarcinoma cell line derived from pancreatic tissue of a male C57BL/6 mouse. The cells were induced with 3-methylcholanthrene and are classified as a mouse pancreatic cancer cell line.
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.
For research use only. Not intended for human or animal clinical trials, therapeutic or diagnostic use





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