
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.
PRKDC (protein kinase, DNA-activated, catalytic subunit) encodes the catalytic subunit of DNA-dependent protein kinase (DNA-PK), a protein kinase involved in repair of DNA double-strand breaks. PRKDC functions together with the Ku70/Ku80 heterodimer and phosphorylates proteins involved in DNA repair and recombination. As a member of the phosphatidylinositol 3-kinase-related kinase family, it plays an essential role in maintaining genome integrity following DNA damage.
HT-1080 is a human fibrosarcoma cell line established from a tumor arising adjacent to the acetabulum of a 35-year-old male patient. The cells are tumorigenic in immunodeficient mice and exhibit susceptibility to infection by several RNA tumor viruses. HT-1080 is widely used as a model for studying fibrosarcoma biology, tumor progression, extracellular matrix-related mechanisms, and cancer research.
Before delivery, each clone is authenticated by STR, tested for sterility and mycoplasma, and genotype‑verified by two‑round PCR‑sequencing. Comprehensive QC data accompany every shipment to support reproducible research.

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.

Knockout Region: E1
Reference Transcript: PRKDC-201
Validation Method: PCR amplification+Sanger sequencing
For research use only. Not intended for human or animal clinical trials, therapeutic or diagnostic use





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