
Ubigene gene knockout cell lines mediated by optimized CRISPR-Cas9 technology provide reliable in vitro models for investigating gene function, signaling pathways, disease mechanisms, and therapeutic targets.
GSDME (gasdermin E) encodes a protein whose expression has been detected in the fetal cochlea and that has been implicated in nonsyndromic hearing impairment. The available annotation does not establish a specific molecular function or cellular pathway for GSDME. Genetic alterations in GSDME are associated with hearing impairment, suggesting an important role in auditory system development or function, although the mechanisms connecting GSDME activity with cochlear physiology remain incompletely characterized.
The A2058 cell line was established from a lymph node metastasis of malignant melanoma in a 43-year-old male patient. The cells exhibit highly invasive properties and have been used as a source for studying proteins associated with cellular invasion, including type IV collagenase, tissue inhibitor of metalloproteinase-2 (TIMP-2), and autocrine motility factor. A2058 is used as a human melanoma model for investigating tumor invasion and metastasis-related mechanisms.
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.
For research use only. Not intended for human or animal clinical trials, therapeutic or diagnostic use





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