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Membrane transport protein XK (XK) (AA 83-111), (N-Term) anticorps

Cet anticorps Lapin Polyclonal détecte spécifiquement dans WB. Il présente une réactivité envers Humain.
N° du produit ABIN5530187

Aperçu rapide pour Membrane transport protein XK (XK) (AA 83-111), (N-Term) anticorps (ABIN5530187)

Antigène

Voir toutes Membrane transport protein XK (XK) Anticorps
Membrane transport protein XK (XK)

Reactivité

  • 19
  • 6
  • 6
  • 4
  • 3
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
Humain

Hôte

  • 18
  • 1
Lapin

Clonalité

  • 19
Polyclonal

Conjugué

  • 12
  • 2
  • 2
  • 1
  • 1
  • 1
Inconjugué

Application

  • 17
  • 11
  • 2
  • 1
Western Blotting (WB)
  • Épitope

    • 8
    • 6
    • 3
    • 1
    • 1
    • 1
    AA 83-111, N-Term

    Purification

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

    Immunogène

    This XK antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 83-111 amino acids from the N-terminal region of human XK.

    Isotype

    Ig Fraction
  • Indications d'application

    For WB starting dilution is: 1:1000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    0.5 mg/mL

    Buffer

    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

    Store at 4°C for three months and -20°C, stable for up to one year. As with all antibodies care should be taken to avoid repeated freeze thaw cycles. Antibodies should not be exposed to prolonged high temperatures.
  • Antigène

    Membrane transport protein XK (XK)

    Autre désignation

    XK

    Sujet

    This locus controls the synthesis of the Kell blood group 'precursor substance' (Kx). Mutations in this gene have been associated with McLeod syndrome, an X-linked, recessive disorder characterized by abnormalities in the neuromuscular and hematopoietic systems. The encoded protein has structural characteristics of prokaryotic and eukaryotic membrane transport proteins.

    Poids moléculaire

    51 kDa

    ID gène

    7504

    UniProt

    P51811
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