Tel:
+49 (0)241 95 163 153
Fax:
+49 (0)241 95 163 155
E-Mail:
orders@anticorps-enligne.fr

Nyctalopin anticorps (N-Term)

L’anticorps Lapin Polyclonal anti-Nyctalopin a été validé pour WB et EIA. Il convient pour détecter Nyctalopin dans des échantillons de Humain.
N° du produit ABIN953798

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

Antigène

Voir toutes Nyctalopin (NYX) Anticorps
Nyctalopin (NYX)

Reactivité

  • 11
  • 1
Humain

Hôte

  • 11
Lapin

Clonalité

  • 11
Polyclonal

Conjugué

  • 6
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp Nyctalopin est non-conjugé

Application

  • 11
  • 9
  • 2
Western Blotting (WB), Enzyme Immunoassay (EIA)
  • Épitope

    • 8
    • 2
    • 2
    • 1
    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
  • Indications d'application

    Optimal working dilution should be determined by the investigator.

    Restrictions

    For Research Use only
  • 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.
  • 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
Vous êtes ici:
Chat with us!