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HAP1 antibody (Center)

HAP1 Reactivity: Human, Mouse, Rat WB, IHC (p), EIA Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN499942
  • Target See all HAP1 Antibodies
    HAP1 (Huntingtin Associated Protein 1 (HAP1))
    Binding Specificity
    • 4
    • 3
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Center
    Reactivity
    Human, Mouse, Rat
    Host
    • 11
    • 3
    • 2
    Rabbit
    Clonality
    • 14
    • 2
    Polyclonal
    Conjugate
    • 13
    • 1
    • 1
    • 1
    This HAP1 antibody is un-conjugated
    Application
    • 12
    • 6
    • 6
    • 3
    • 2
    • 2
    • 1
    • 1
    Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Enzyme Immunoassay (EIA)
    Specificity
    This antibody reacts to HAP1.
    Purification
    Affinity chromatography purified via peptide column
    Immunogen
    HAP1 antibody was raised against a 19 amino acid peptide from near the center of human HAP1.
    Isotype
    IgG
    Top Product
    Discover our top product HAP1 Primary Antibody
  • Application Notes
    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.
    Restrictions
    For Research Use only
  • Buffer
    PBS containing 0.02 % sodium azide.
    Preservative
    Sodium azide
    Precaution of Use
    This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Storage
    4 °C
    Storage Comment
    Store the antibody undiluted at 2-8 °C.
  • Target
    HAP1 (Huntingtin Associated Protein 1 (HAP1))
    Alternative Name
    HAP1 (HAP1 Products)
    Synonyms
    HAP2 antibody, HIP5 antibody, HLP antibody, hHLP1 antibody, HAP1-A antibody, HAP1-B antibody, HAP-1 antibody, huntingtin associated protein 1 antibody, huntingtin-associated protein 1 antibody, HAP1 antibody, Hap1 antibody
    Background
    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
    Gene ID
    9001
    UniProt
    P54257
    Pathways
    Cell RedoxHomeostasis, Smooth Muscle Cell Migration, Positive Regulation of Response to DNA Damage Stimulus
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