Nyctalopin anticorps (N-Term)

N° du produit ABIN653436

Détail du produit anti-Nyctalopin anticorps

Antigène: Nyctalopin (NYX)

Épitope: AA 53-80, N-Term

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp Nyctalopin est non-conjugé

Application: Western Blotting (WB)

Purification: This antibody is purified through a protein A column, followed by peptide affinity purification.

Immunogène: This NYX antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 53-80 amino acids from the N-terminal region of human NYX.

Clone: RB23621

Isotype: Ig Fraction

Information d'application

Indications d'application: WB: 1:1000

Restrictions: For Research Use only

Stockage

Format: Liquid

Buffer: Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.

Agent conservateur: Sodium azide

Précaution d'utilisation: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Stock: 4 °C,-20 °C

Stockage commentaire: Maintain refrigerated at 2-8 °C for up to 6 months. For long term storage store at -20 °C in small aliquots to prevent freeze-thaw cycles.

Date de péremption: 6 months

Détails sur Nyctalopin

Antigène: Nyctalopin (NYX)

Autre désignation: NYX (NYX Produits)

Synonymes: anticorps MGC84276, anticorps CLRP, anticorps CSNB1, anticorps CSNB1A, anticorps CSNB4, anticorps NBM1, anticorps CLNP, anticorps nob, anticorps RGD1561300, anticorps nyctalopin, anticorps nyctalopin L homeolog, anticorps uncharacterized LOC491837, anticorps NYX, anticorps nyx.L, anticorps LOC491837, anticorps nyx, anticorps Nyx

Sujet: 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].

Poids moléculaire: 52000

ID gène: 60506

NCBI Accession: NP_072089

UniProt: Q9GZU5