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HAP1 Antikörper (Center)

HAP1 Reaktivität: Human, Maus, Ratte WB, IHC (p), EIA Wirt: Kaninchen Polyclonal unconjugated
Produktnummer ABIN499942
  • Target Alle HAP1 Antikörper anzeigen
    HAP1 (Huntingtin Associated Protein 1 (HAP1))
    Bindungsspezifität
    • 4
    • 3
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Center
    Reaktivität
    Human, Maus, Ratte
    Wirt
    • 11
    • 4
    • 2
    Kaninchen
    Klonalität
    • 14
    • 3
    Polyklonal
    Konjugat
    • 14
    • 1
    • 1
    • 1
    Dieser HAP1 Antikörper ist unkonjugiert
    Applikation
    • 13
    • 6
    • 6
    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
    Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Enzyme Immunoassay (EIA)
    Spezifität
    This antibody reacts to HAP1.
    Aufreinigung
    Affinity chromatography purified via peptide column
    Immunogen
    HAP1 antibody was raised against a 19 amino acid peptide from near the center of human HAP1.
    Isotyp
    IgG
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  • Applikationshinweise
    ELISA. Western Blot: 0.5 - 1 μg/mL. Immunohistochemistry.
    Other applications not tested.
    Optimal dilutions are dependent on conditions and should be determined by the user.
    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Buffer
    PBS containing 0.02 % sodium azide.
    Konservierungsmittel
    Sodium azide
    Vorsichtsmaßnahmen
    This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Lagerung
    4 °C
    Informationen zur Lagerung
    Store the antibody undiluted at 2-8 °C.
  • Target
    HAP1 (Huntingtin Associated Protein 1 (HAP1))
    Andere Bezeichnung
    HAP1 (HAP1 Produkte)
    Synonyme
    HAP2 antikoerper, HIP5 antikoerper, HLP antikoerper, hHLP1 antikoerper, HAP1-A antikoerper, HAP1-B antikoerper, HAP-1 antikoerper, huntingtin associated protein 1 antikoerper, huntingtin-associated protein 1 antikoerper, HAP1 antikoerper, Hap1 antikoerper
    Hintergrund
    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. HAP1 was initially identified through a two-hybrid library screening, the binding of HAP1 to huntingtin correlated with the expansion of the polyglutamine tract. HAP1 also interacts with two cytoskeletal proteins (dynactin and pericentriolar autoantigen protein 1), suggesting that HAP1 may play a role in vesicular trafficking or organelle transport. HAP1 is also involved with the huntingtin-enhanced BDNF transport along the cellular microtubles. Attenuation of this process led to the loss of neurotrophic support and neuronal toxicity, which suggests that loss of this function might contribute to pathogenesis. Several alternatively spliced isoforms have been described for HAP1.Synonyms: HAP-1, HAP2, HLP1, Huntingtin-associated protein 1, Neuroan 1
    Gen-ID
    9001
    UniProt
    P54257
    Pathways
    Cell RedoxHomeostasis, Smooth Muscle Cell Migration, Positive Regulation of Response to DNA Damage Stimulus
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