Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
RD3 is preferentially expressed in retina.Defects in RD3 are the cause of Leber congenital amaurosis type 12 (LCA12).
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
Protein Aliases: Protein RD3; Retinal degeneration protein 3
Gene Aliases: 3322402L07Rik; C1orf36; LCA12; rd-3; RD3
UniProt ID: (Human) Q7Z3Z2, (Mouse) Q8BRE0
Entrez Gene ID: (Human) 343035, (Mouse) 74023
If an Invitrogen™ antibody doesn't perform as described on our website or datasheet,we'll replace the product at no cost to you, or provide you with a credit for a future purchase.*
Learn moreGet expert recommendations for common problems or connect directly with an on staff expert for technical assistance related to applications, equipment and general product use.
Contact tech support