
CRISPR knockout cell lines are engineered through targeted genome editing to eliminate gene function, supporting studies of cellular biology, disease mechanisms, and drug discovery.
ZFYVE16 (zinc finger FYVE-type containing 16) encodes an endosomal FYVE zinc finger protein involved in membrane trafficking. The protein functions as a scaffold in transforming growth factor-beta signaling and participates in both positive and negative feedback regulation of bone morphogenetic protein signaling. Through its endosomal localization and protein-interaction functions, ZFYVE16 may coordinate membrane trafficking with intracellular signaling pathways.
A human esophageal cancer cell line established from a poorly differentiated squamous cell carcinoma of the upper cervical esophagus in a 49-year-old woman after radiotherapy. KYSE-150 carries amplified c-erb-B and cyclin D1 oncogenes and has been reported to produce tumors in nude mice. The cell line has been extensively characterized and is included in large-scale cancer cell line resources.
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.

Targeted knockout region: EExon 4
Reference Transcript: NM_001105251
Frameshift Mutation Strategy
For research use only. Not intended for human or animal clinical trials, therapeutic or diagnostic use





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