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RD3


Official Full Name
RD3 regulator of GUCY2D
Organism
Homo sapiens
Gene ID
343035
Background
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]
Synonyms
LCA12; C1orf36

Cat.No. Product Name Price
LV23762L human RD3 (NM_183059) lentivirus particles Inquiry
Cat.No. Product Name Price
SHH391408 shRNA set against Human RD3 (NM_183059.2) Inquiry
SHH391412 shRNA set against Mouse RD3 (NM_023727.3) Inquiry
SHW011006 shRNA set against Danio rerio RD3 (NM_001080631) Inquiry
Cat.No. Product Name Price
CDCS408770 Human RD3 ORF Clone (BC065541) Inquiry
CDFG021558 Mouse Rd3 cDNA Clone(NM_001177900.1) Inquiry
CDFH016105 Human RD3 cDNA Clone(NM_001164688.1) Inquiry
MiUTR4H-TG07420 RD3 miRNA 3'UTR clone Inquiry
CDCB172481 Danio rerio RD3 ORF Clone (NM_001080631) Inquiry
CDCB189158 Rabbit RD3 ORF clone (XM_002717416.2) Inquiry
CDCH072674 Mouse Rd3 ORF clone (NM_001177900.1) Inquiry
CDCR354819 Human RD3 ORF Clone(NM_001164688.1) Inquiry
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