Nyctalopin anticorps (N-Term)

N° du produit ABIN953798

L’anticorps anti-Nyctalopin Polyclonal Lapin est utilisé pour la détection de Nyctalopin dans des échantillons de Humain. Il a été validé pour WB et EIA.

Aperçu rapide pour Nyctalopin anticorps (N-Term) (ABIN953798)

Antigène: Nyctalopin (NYX)

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp Nyctalopin est non-conjugé

Application: Western Blotting (WB), Enzyme Immunoassay (EIA)

Détail du produit anti-Nyctalopin anticorps

Épitope: AA 59-89, N-Term

Specificité: This antibody recognizes Human Nyctalopin (N-term).

Purification: Protein A column, followed by peptide affinity purification

Immunogène: KLH conjugated synthetic peptide between 59~89 amino acids from the N-terminal region of Human Nyctalopin. Genename: NYX

Isotype: Ig Fraction

Information d'application

Indications d'application: Optimal working dilution should be determined by the investigator.

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 0.25 mg/mL

Buffer: PBS containing 0.09 % (W/V) Sodium Azide as preservative

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.

Conseil sur la manipulation: Avoid repeated freezing and thawing.

Stock: 4 °C/-20 °C

Stockage commentaire: Store undiluted at 2-8 °C for one month or (in aliquots) at -20 °C for longer.

Détails sur Nyctalopin

Antigène: Nyctalopin (NYX)

Autre désignation: Nyctalopin

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].Synonyms: CLRP, NYX

Poids moléculaire: 52000 Da

ID gène: 60506

NCBI Accession: NP_072089