Gene: RD3
Official Full Name: RD3 regulator of GUCY2Dprovided by HGNC
Gene Summary: This gene encodes a retinal protein that is associated with promyelocytic leukemia-gene product (PML) bodies in the nucleus. Mutations in this gene cause Leber congenital amaurosis type 12, a disease that results in retinal degeneration. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2009]
| Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
|---|---|---|---|---|---|---|
| KOA02977 | RD3 Knockout cell line (AC16) | Human | RD3 | 1:3-1:4 | negative | Online Inquiry |
| KOA18424 | RD3 Knockout cell line (BEAS-2B) | Human | RD3 | 1:3~1:4 | negative | Online Inquiry |
| KOA33874 | RD3 Knockout cell line (U-2932) | Human | RD3 | 1:2-1:4 | negative | Online Inquiry |
| KOA49281 | RD3 Knockout cell line (TPC-1) | Human | RD3 | 1:5-1:8 | negative | Online Inquiry |
| KOA64682 | RD3 Knockout cell line (NCM460) | Human | RD3 | 1:2~1:3 | negative | Online Inquiry |
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