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HAP1 antibody (AA 1-671) (Cy3)

The Rabbit Polyclonal anti-HAP1 antibody is suitable to detect HAP1 in samples from Human, Mouse and Rat. It has been validated for FACS.
Catalog No. ABIN7998445
$570.00
Plus shipping costs $50.00
100 μg
Shipping to: United States
Delivery in 4 to 7 Business Days

Quick Overview for HAP1 antibody (AA 1-671) (Cy3) (ABIN7998445)

Target

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

Reactivity

Human, Mouse, Rat

Host

  • 27
  • 3
  • 2
Rabbit

Clonality

  • 30
  • 2
Polyclonal

Conjugate

  • 20
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This HAP1 antibody is conjugated to Cy3

Application

  • 21
  • 12
  • 11
  • 10
  • 8
  • 8
  • 5
  • 2
  • 1
  • 1
Flow Cytometry (FACS)
  • Binding Specificity

    • 14
    • 4
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 1-671

    Purpose

    Anti-HAP1 Antibody Cy3 Conjugated

    Cross-Reactivity (Details)

    No cross-reactivity with other proteins.

    Purification

    Immunogen affinity purified.

    Immunogen

    E.coli-derived human HAP1 recombinant protein (Position: M1-R671).

    Isotype

    IgG
  • Application Notes

    Flow Cytometry, 1-3 μg/1x106 cells

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    Each vial contains 50 % glycerol, 0.9 % NaCl, 0.2 % Na2HPO4, 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

    -20 °C

    Storage Comment

    At -20°C for one year from date of receipt. Avoid repeated freezing and thawing. Protect from light.

    Expiry Date

    12 months
  • Target

    HAP1 (Huntingtin Associated Protein 1 (HAP1))

    Alternative Name

    HAP1

    Background

    Background: 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.

    Gene Full Name: huntingtin associated protein 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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