
CRISPR knockout cell lines are engineered through targeted genome editing to eliminate gene function, supporting studies of cellular biology, disease mechanisms, and drug discovery.
NECTIN4 (nectin cell adhesion molecule 4) encodes a single-pass transmembrane cell adhesion molecule of the nectin family. It mediates cell-cell adhesion through homophilic and heterophilic interactions and can undergo proteolytic cleavage to generate a soluble form. NECTIN4 therefore contributes to organization of epithelial and other cellular contacts and is relevant to studies of cell adhesion, membrane signaling, and tissue organization. Mutations in NECTIN4 cause ectodermal dysplasia-syndactyly syndrome type 1.
A human bladder cancer model, SW780 originated from a primary urinary bladder transitional cell carcinoma of a 53-year-old female. The cells are classified as a human bladder carcinoma cell line and retain epithelial characteristics associated with their tumor origin. SW780 has been characterized through genomic and transcriptomic analyses and is represented in major cancer cell line resources.
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.

Knockout Region: E2
Reference Transcript: NECTIN4-201
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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