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RD3 Full-Length MS Protein Standard

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Product Description


NameRD3 Full-Length MS Protein Standard
Cat#CPFL309596
Protein Nameretinal degeneration 3
SymbolRD3
SynonymsC1orf36; LCA12
AccessionNM_183059
Cytogenetic1q32.3
Amino Acid Labeled[U- 13C6, 15N4]-L-Arg and [U- 13C6, 15N2]-L-Lys
DescriptionRD3 Full-Length MS Protein Standard (NP_898882), Labeled with [U- 13C6, 15N4]-L-Arginine and [U- 13C6, 15N2]-L-Lysine, was produced in human 293 cells (HEK293) with fully chemically defined cell culture medium to obtain incorporation efficiency at Creative-Proteomics. 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.

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