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CLCN2 anticorps (N-Term)

L’anticorps Lapin Polyclonal anti-CLCN2 a été validé pour WB. Il convient pour détecter CLCN2 dans des échantillons de Humain et Souris.
N° du produit ABIN5530908

Aperçu rapide pour CLCN2 anticorps (N-Term) (ABIN5530908)

Antigène

Voir toutes CLCN2 Anticorps
CLCN2 (Chloride Channel 2 (CLCN2))

Reactivité

  • 29
  • 20
  • 12
  • 1
  • 1
Humain, Souris

Hôte

  • 28
  • 1
  • 1
Lapin

Clonalité

  • 29
  • 1
Polyclonal

Conjugué

  • 14
  • 3
  • 3
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp CLCN2 est non-conjugé

Application

  • 17
  • 16
  • 3
  • 3
  • 1
  • 1
  • 1
  • 1
Western Blotting (WB)
  • Épitope

    • 8
    • 5
    • 3
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    AA 209-237, N-Term

    Purification

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

    Immunogène

    This CLCN2 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 209-237 amino acids from the N-terminal region of human CLCN2.

    Isotype

    Ig Fraction
  • Indications d'application

    For WB starting dilution is: 1:1000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    0.45 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

    CLCN2 (Chloride Channel 2 (CLCN2))

    Autre désignation

    CLCN2

    Sujet

    The transmembrane protein encoded by this gene is a voltage-gated chloride channel that maintains chloride ion homeostasis in various cells. Defects in this gene may be a cause of certain epilepsies. Four transcript variants encoding different isoforms have been found for this gene.

    Poids moléculaire

    99 kDa

    ID gène

    1181

    UniProt

    P51788
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