
CRISPR knockout cell lines are engineered through targeted genome editing to eliminate gene function, supporting studies of cellular biology, disease mechanisms, and drug discovery.
NEDD4L (NEDD4 like E3 ubiquitin protein ligase) encodes a HECT domain E3 ubiquitin ligase that transfers ubiquitin to specific protein substrates, promoting their regulated degradation. NEDD4L regulates the cell-surface abundance of epithelial sodium channels and thereby contributes to epithelial sodium transport. Its ubiquitin ligase activity provides a mechanism for controlling membrane protein turnover and associated cellular signaling processes.
JAR is a human choriocarcinoma cell line established from a trophoblastic tumor of the placenta of a 24-year-old woman. The cell line originates from a male fetus and represents a trophoblast-derived tumor model. JAR is used for studies of placental biology, trophoblast differentiation, and mechanisms involved in gestational cancers.
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 9
Reference Transcript: NM_001144967
Frameshift Mutation Strategy
For research use only. Not intended for human or animal clinical trials, therapeutic or diagnostic use






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