
CRISPR knockout cell lines are engineered through targeted genome editing to eliminate gene function, supporting studies of cellular biology, disease mechanisms, and drug discovery.
TBC1D31 (TBC1 domain family member 31) encodes a protein with molecular adaptor activity that is involved in cilium assembly. It localizes to the Golgi apparatus, centriolar satellites, and ciliary basal body, positioning it within cellular structures that coordinate centrosomal and ciliary organization. TBC1D31 therefore contributes to assembly and maintenance of primary ciliary structures.
The ARPE-19 cell line is a spontaneously arising human retinal pigment epithelial (RPE) cell line established in 1986 by Amy Aotaki-Keen from the normal eyes of a 19-year-old male donor. The cells exhibit characteristic RPE morphology, including the ability to form cobblestone-like monolayers and develop pigmentation during long-term culture. ARPE-19 provides a widely used in vitro model for studying retinal pigment epithelium biology, retinal function, ocular disease mechanisms, and cellular responses relevant to vision research.
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.

Knockout Region: E4
Reference Transcript: TBC1D31-201
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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