Recombinant Human NYX Protein, MYC/DDK-tagged

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Recombinant Human NYX Protein, MYC/DDK-tagged

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Cat.No. : NYX-1850H
Product Overview : Recombinant human NYX protein, fused to MYC/DDK-tagged at C-terminus, was expressed in HEK293
Description : 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].
Source : HEK293
Species : Human
Tag : MYC/DDK
Form : 25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10% glycerol.
Molecular Mass : 49.5 kDa
Purity : > 80% as determined by SDS-PAGE and Coomassie blue staining
Concentration : >50 ug/mL as determined by microplate BCA method
Gene Name : NYX nyctalopin [ Homo sapiens ]
Official Symbol : NYX
Synonyms : CLRP; CSNB1; CSNB1A; CSNB4; NBM1
Gene ID : 60506
mRNA Refseq : NM_022567
Protein Refseq : NP_072089
MIM : 300278
UniProt ID : Q9GZU5

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