
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.
The Jurkat, Clone E6-1 cell line was established from the peripheral blood of a 14-year-old male patient and is a derivative of the Jurkat T-lymphocytic cell line. This clone was generated from Jurkat E6-1 cells through gamma irradiation and complement-mediated selection using anti-CD45 antibodies. It exhibits markedly reduced CD45 expression (5–8% of the parental line), resulting in impaired signal transduction through the T-cell receptor (TcR) complex and the accessory molecule CD2. The cells can produce interleukin-2 (IL-2) following stimulation with calcium ionophore and phorbol ester but show defective IL-2 production after TcR or CD2 activation. This cell line is used as a model for studying T-cell signaling pathways and immune regulation.
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 7
Reference Transcript: NM_001347423
Frameshift Mutation Strategy
For research use only. Not intended for human or animal clinical trials, therapeutic or diagnostic use






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