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HAP1 antibody (C-Term)

The Goat Polyclonal anti-HAP1 antibody is suitable to detect HAP1 in samples from Mouse and Rat. It has been validated for WB and EIA.
Catalog No. ABIN615992
$750.00
Plus shipping costs $50.00
0.1 mg
Shipping to: United States
Delivery in 1 to 2 Business Days

Quick Overview for HAP1 antibody (C-Term) (ABIN615992)

Target

See all HAP1 Antibodies
HAP1 (Huntingtin Associated Protein 1 (HAP1))

Reactivity

  • 16
  • 10
  • 9
Mouse, Rat

Host

  • 17
  • 3
  • 2
Goat

Clonality

  • 20
  • 2
Polyclonal

Conjugate

  • 19
  • 1
  • 1
  • 1
This HAP1 antibody is un-conjugated

Application

  • 18
  • 9
  • 9
  • 8
  • 7
  • 4
  • 2
  • 2
  • 1
  • 1
Western Blotting (WB), Enzyme Immunoassay (EIA)
  • Binding Specificity

    • 4
    • 4
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    C-Term

    Sequence

    C-QDAHSKRQQK QK

    Specificity

    Recognizes Mouse Hap1

    Cross-Reactivity (Details)

    Species reactivity (expected):Rat.
    Species reactivity (tested):Mouse.

    Purification

    Ammonium Sulphate Precipitation followed by antigen Affinity Chromatography using the immunizing peptide.

    Immunogen

    Peptide with sequence from the C Terminus of the protein sequence according to NP_034534.1. Genename: Hap1
  • Application Notes

    Optimal working dilution should be determined by the investigator.

    Restrictions

    For Research Use only
  • Concentration

    0.5 mg/mL

    Buffer

    Tris saline, pH 7.3 containing 0.02 % Sodium Azide as preservative and 0.5 % BSA as stabilizer.

    Preservative

    Sodium azide

    Precaution of Use

    This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Handling Advice

    Avoid repeated freezing and thawing.

    Storage

    4 °C/-20 °C

    Storage Comment

    Store the antibody undiluted at 2-8 °C for one month or (in aliquots) at -20 °C for longer.
  • Target

    HAP1 (Huntingtin Associated Protein 1 (HAP1))

    Alternative Name

    HAP1

    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. It is a progressive disorder that generally begins in middle age with abnormalities of movement, cognition, personality and mood. HAP-1 is highly expressed in brain and shown to mediate the neuropathology of HD. The human protein 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. Two transcripts encoding different isoforms have been identified but one is a nonsense-mediated decay (NMD) candidate.Synonyms: HAP-1, HAP2, HLP1, Huntingtin-associated protein 1, Neuroan 1

    Gene ID

    15114

    NCBI Accession

    NP_034534

    UniProt

    O35668

    Pathways

    Cell RedoxHomeostasis, Smooth Muscle Cell Migration, Positive Regulation of Response to DNA Damage Stimulus
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