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DRD4 antibody (AA 57-387)

This Rabbit Polyclonal antibody specifically detects DRD4 in WB, ELISA and FACS. It exhibits reactivity toward Mouse and Rat.
Catalog No. ABIN7875806
$625.62
Plus shipping costs $50.00
100 μg
Shipping to: United States
Delivery in 2 to 4 Business Days

Quick Overview for DRD4 antibody (AA 57-387) (ABIN7875806)

Target

See all DRD4 Antibodies
DRD4 (Dopamine Receptor D4 (DRD4))

Reactivity

  • 61
  • 47
  • 16
  • 1
  • 1
  • 1
  • 1
Mouse, Rat

Host

  • 58
  • 10
Rabbit

Clonality

  • 57
  • 10
Polyclonal

Conjugate

  • 30
  • 4
  • 4
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This DRD4 antibody is un-conjugated

Application

  • 53
  • 28
  • 13
  • 13
  • 10
  • 8
  • 5
  • 5
  • 4
  • 3
  • 3
  • 1
  • 1
Western Blotting (WB), ELISA, Flow Cytometry (FACS)
  • Binding Specificity

    • 15
    • 8
    • 5
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 57-387

    Purpose

    Drd4 Antibody

    Purification

    Affinity purified

    Immunogen

    Recombinant mouse protein (amino acids A57-C387) was used as the immunogen for the Drd4 antibody.

    Isotype

    IgG
  • Application Notes

    Optimal dilution of the Drd4 antibody should be determined by the researcher.

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Buffer

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

    Storage

    4 °C,-20 °C

    Storage Comment

    After reconstitution, the Drd4 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

    DRD4 (Dopamine Receptor D4 (DRD4))

    Alternative Name

    Drd4

    Background

    D(4) dopamine receptor is aproteinthat in humans is encoded by the Drd4gene. This gene encodes a protein that is necessary for the repair of ultraviolet light-damaged DNA. This protein is the smaller subunit of a heterodimeric protein complex that participates in nucleotide excision repair, and this complex mediates the ubiquitylation of histones H3 and H4, which facilitates the cellular response to DNA damage. And this subunit appears to be required for DNA binding. Mutations in this gene cause xeroderma pigmentosum complementation group E, a recessive disease that is characterized by an increased sensitivity to UV light and a high predisposition for skin cancer development, in some cases accompanied by neurological abnormalities. Two transcript variants encoding different isoforms have been found for this gene.

    UniProt

    P51436

    Pathways

    cAMP Metabolic Process, Synaptic Membrane, Proton Transport, Photoperiodism, Negative Regulation of Transporter Activity
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