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

HAP1 anticorps (AA 1-671)

L’anticorps anti-HAP1 Polyclonal Lapin est utilisé pour la détection de HAP1 dans des échantillons de Humain, Souris et Rat. Il a été validé pour WB, ELISA, IF et FACS.
N° du produit ABIN7869522
644,88 €
Plus frais de livraison 40,00 € et TVA
100 μg
Destination: France
Envoi sous 6 à 9 jours ouvrables

Aperçu rapide pour HAP1 anticorps (AA 1-671) (ABIN7869522)

Antigène

Voir toutes HAP1 Anticorps
HAP1 (Huntingtin Associated Protein 1 (HAP1))

Reactivité

Humain, Souris, Rat

Hôte

  • 16
  • 4
  • 2
Lapin

Clonalité

  • 19
  • 3
Polyclonal

Conjugué

  • 19
  • 1
  • 1
  • 1
Cet anticorp HAP1 est non-conjugé

Application

  • 18
  • 9
  • 8
  • 8
  • 7
  • 4
  • 2
  • 1
  • 1
  • 1
Western Blotting (WB), ELISA, Immunofluorescence (IF), Flow Cytometry (FACS)
  • Épitope

    • 4
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 1-671

    Fonction

    Huntingtin-associated protein 1 Antibody / HAP1

    Purification

    Antigen affinity purified

    Immunogène

    Recombinant human protein (amino acids M1-R671) was used as the immunogen for the Huntingtin-associated protein 1 antibody.

    Isotype

    IgG
  • Indications d'application

    Optimal dilution of the Huntingtin-associated protein 1 antibody should be determined by the researcher.

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Buffer

    0.5 mg/mL if reconstituted with 0.2 mL sterile DI water

    Stock

    4 °C,-20 °C

    Stockage commentaire

    After reconstitution, the Huntingtin-associated protein 1 antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.
  • Antigène

    HAP1 (Huntingtin Associated Protein 1 (HAP1))

    Autre désignation

    Huntingtin-associated protein 1

    Sujet

    Huntingtin-associated protein 1 (HAP1) is a protein which in humans is encoded by the HAP1 gene. Huntington's disease (HD), a neurodegenerative disorder characterized by loss of striatal neurons, is caused by an expansion of a polyglutamine tract in the HD protein huntingtin. This gene encodes a protein that interacts with huntingtin, with two cytoskeletal proteins (dynactin and pericentriolar autoantigen protein 1), and with a hepatocyte growth factor-regulated tyrosine kinase substrate. The interactions with cytoskeletal proteins and a kinase substrate suggest a role for this protein in vesicular trafficking or organelle transport. Several alternatively spliced transcript variants encoding different isoforms have been described for this gene.

    UniProt

    P54257

    Pathways

    Cell RedoxHomeostasis, Smooth Muscle Cell Migration, Positive Regulation of Response to DNA Damage Stimulus
Vous êtes ici:
Chat with us!