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HAP1 Antikörper (AA 1-671)

Der Kaninchen Polyklonal anti-HAP1 Antikörper wird verwendet zum Nachweis von HAP1 in Proben von Human, Maus und Ratte. Er wurde validiert für WB, ELISA, IF und FACS.
Produktnummer ABIN7869522
644,88 €
Zzgl. Versandkosten 20,00 € und MwSt
100 μg
Lieferung nach: Deutschland
Lieferung in 6 bis 9 Werktagen

Kurzübersicht für HAP1 Antikörper (AA 1-671) (ABIN7869522)

Target

Alle HAP1 Antikörper anzeigen
HAP1 (Huntingtin Associated Protein 1 (HAP1))

Reaktivität

Human, Maus, Ratte

Wirt

  • 16
  • 4
  • 2
Kaninchen

Klonalität

  • 19
  • 3
Polyklonal

Konjugat

  • 19
  • 1
  • 1
  • 1
Dieser HAP1 Antikörper ist unkonjugiert

Applikation

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

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

    Verwendungszweck

    Huntingtin-associated protein 1 Antibody / HAP1

    Aufreinigung

    Antigen affinity purified

    Immunogen

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

    Isotyp

    IgG
  • Applikationshinweise

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

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Lyophilized

    Buffer

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

    Lagerung

    4 °C,-20 °C

    Informationen zur Lagerung

    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.
  • Target

    HAP1 (Huntingtin Associated Protein 1 (HAP1))

    Andere Bezeichnung

    Huntingtin-associated protein 1

    Hintergrund

    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
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