NYX

Nyctalopin

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.

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Proteins (3)

Type

Over-Expression Lysate (2)

Recombinant (1)

Target

NYX (3)

Publications

No (3)

Tag

Myc-DDK (Flag) (3)

Species

Human (2)

Source

293T Cells (1)

HEK 293 Cells (2)

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Human NYX Protein (Recombinant Myc-DDK (Flag)) (Full Length) - LS-G72187

Source:

HEK 293 Cells

Tag:

Myc-DDK (Flag)

Molecular Weight:

49.5 kDa

Price:

20 µg/$1,107

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NYX Protein (Over-Expression Lysate Myc-DDK (Flag)) (Full Length) - LS-G110320

Source:

HEK 293 Cells

Tag:

Myc-DDK (Flag)

Molecular Weight:

49.5 kDa

Price:

100 µg/$710

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Human NYX Protein (Over-Expression Lysate Myc-DDK (Flag)) (Full Length) - LS-G91646

Source:

293T Cells

Tag:

Myc-DDK (Flag)

Molecular Weight:

49.5 kDa

Price:

20 µg/$215

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