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Invitrogen
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The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen and the purity is > 95% (by SDS-PAGE).
The product of this gene belongs to the small leucine-rich proteoglycan (SLRP) family of proteins. Defects in this gene are the cause of congenital stationary night blindness type 1 (CSNB1), also called X-linked congenital stationary night blindness (XLCSNB). CSNB1 is a rare inherited retinal disorder characterized by impaired scotopic vision, myopia, hyperopia, nystagmus and reduced visual acuity. The role of other SLRP proteins suggests that mutations in this gene disrupt developing retinal interconnections involving the ON-bipolar cells, leading to the visual losses seen in patients with complete CSNB.
仅用于科研。不用于诊断过程。未经明确授权不得转售。
蛋白别名: leucine-rich repeat protein; no b wave; Nyctalopin
基因别名: CLNP; CLRP; CSNB1; CSNB1A; CSNB4; NBM1; nob; NYX
UniProt ID: (Human) Q9GZU5, (Mouse) P83503
Entrez Gene ID: (Human) 60506, (Mouse) 236690