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HAX1 anticorps

Cet anticorps Lapin Polyclonal détecte spécifiquement HAX1 dans WB et ELISA. Il présente une réactivité envers Humain, Souris et Rat.
N° du produit ABIN7114867

Aperçu rapide pour HAX1 anticorps (ABIN7114867)

Antigène

Voir toutes HAX1 Anticorps
HAX1 (HCLS1 Associated Protein X-1 (HAX1))

Reactivité

  • 63
  • 22
  • 19
  • 4
  • 4
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
Humain, Souris, Rat

Hôte

  • 52
  • 10
  • 1
Lapin

Clonalité

  • 54
  • 9
Polyclonal

Conjugué

  • 34
  • 5
  • 3
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp HAX1 est non-conjugé

Application

  • 53
  • 28
  • 16
  • 13
  • 13
  • 8
  • 7
  • 4
  • 3
  • 2
  • 2
  • 1
  • 1
Western Blotting (WB), ELISA
  • Fonction

    HAX1 antibody

    Purification

    Immunogen affinity purified

    Pureté

    ≥95 % as determined by SDS-PAGE

    Immunogène

    HCLS1 associated protein X-1

    Isotype

    IgG
  • Indications d'application

    WB: 1:500 - 1:2000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    PBS with 0.02 % sodium azide and 50 % glycerol pH 7.3,

    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 freeze / thaw cycles.

    Stock

    -20 °C

    Stockage commentaire

    -20°C for 12 months

    Date de péremption

    12 months
  • Antigène

    HAX1 (HCLS1 Associated Protein X-1 (HAX1))

    Autre désignation

    HAX1

    Sujet

    Synonyms: HCLS1-associated protein X-1|HS1-associating protein X-1 (HAX-1)|HS1-binding protein 1 (HSP1BP-1)|HAX1|HS1BP1

    Background: The protein encoded by this gene is known to associate with hematopoietic cell-specific Lyn substrate 1, a substrate of Src family tyrosine kinases. It also interacts with the product of the polycystic kidney disease 2 gene, mutations in which are associated with autosomal-dominant polycystic kidney disease, and with the F-actin-binding protein, cortactin. It was earlier thought that this gene product is mainly localized in the mitochondria, however, recent studies indicate it to be localized in the cell body. Mutations in this gene result in autosomal recessive severe congenital neutropenia, also known as Kostmann disease. Two transcript variants encoding different isoforms have been found for this gene.

    Poids moléculaire

    31 kDa, 36 kDa

    UniProt

    O00165

    Pathways

    Regulation of Actin Filament Polymerization
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