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POU4F3

All products and services are For Research Use Only and CANNOT be used in the treatment or diagnosis of disease.

POU4F3 is a member of the POU-domain family of transcription factors which have been observed to play important roles in control of cell identity in several systems. Defects in this gene are the cause of non-syndromic sensorineural deafness autosomal dominant type 15. This protein is found in the retina and may play a role in determining or maintaining the identities of a small subset of visual system neurons.
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CAT Product Name Target Species Antibody Clone Antibody Host Receptor Construction Vector Type Targeting Cell Type CAR Vector Type Inquiry & Datasheet
CAR-YC0196 Anti-POU4F3 (5B8) h(scFv-41BB-CD3ζ) CAR, pCDCAR1 Human 5B8 Mouse scFv-41BB-CD3ζ Lentiviral vector T cell   Add to Cart   Datasheet
CAR-YC1096 Anti-POU4F3 (5B8) h(scFv-CD28-CD3ζ) CAR, pCDCAR1 Human 5B8 Mouse scFv-CD28-CD3ζ Lentiviral vector T cell   Add to Cart   Datasheet
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