Nyctalopin 产品
(Nyctalopin (NYX))
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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].
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Featured Nyctalopin Categories
Nyctalopin 抗体
High quality antibodies with extensive validation data.
Nyctalopin 蛋白
Proteins for various applications incl. WB, ELISA, IF etc.
Recommended Nyctalopin 抗体
Product
Reactivity
Application
Validations
Cat. No.
Quantity
Datasheet
Reactivity
Human
Application
WB, IHC, ELISA
Validations
- (2)
Cat. No.
ABIN7162101
Quantity
100 μL
Datasheet
Datasheet
Reactivity
Human
Application
WB
Validations
Cat. No.
ABIN1810616
Quantity
400 μL
Datasheet
Datasheet
Reactivity
Human
Application
WB, ELISA
Validations
Cat. No.
ABIN2581743
Quantity
200 μL
Datasheet
Datasheet
Recommended 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
Synonyms and alternative names related to Nyctalopin
nyctalopin (NYX), nyctalopin L homeolog (nyx.L), uncharacterized LOC491837 (LOC491837), nyctalopin (nyx), nyctalopin (Nyx), CLNP, CLRP, CSNB1, CSNB1A, CSNB4, MGC84276, NBM1, nob, RGD1561300Protein level used designations for Nyctalopin
- nyctalopin
- leucine-rich repeat protein
- no b wave
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