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Nyctalopin 蛋白

(Nyctalopin (NYX))
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. [provided by RefSeq, Oct 2008].
Nyctalopin Protein (NYX) (Myc-DYKDDDDK Tag) Nyctalopin Protein (NYX) (Myc-DYKDDDDK Tag) Nyctalopin Protein (NYX) (Myc-DYKDDDDK Tag) (ABIN2727840)

NYX 宿主: 人 宿主: HEK-293 Cells Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD

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Popular Nyctalopin 蛋白

Product
Reactivity
Source
Validations
Cat. No.
Quantity
Datasheet
Reactivity Human
Source HEK-293 Cells
Validations
  • (1)
Cat. No. ABIN2727840
Quantity 20 μg
Datasheet Datasheet

Aliases for Nyctalopin 蛋白

nyctalopin (NYX) 蛋白
nyctalopin L homeolog (nyx.L) 蛋白
uncharacterized LOC491837 (LOC491837) 蛋白
nyctalopin (nyx) 蛋白
nyctalopin (Nyx) 蛋白
CLNP 蛋白
CLRP 蛋白
CSNB1 蛋白
CSNB1A 蛋白
CSNB4 蛋白
MGC84276 蛋白
NBM1 蛋白
nob 蛋白
RGD1561300 蛋白
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