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MC3R antibody (AA 91-121)

The Rabbit Polyclonal anti-MC3R antibody has been validated for WB. It is suitable to detect MC3R in samples from Human and Mouse.
Catalog No. ABIN5647192

Quick Overview for MC3R antibody (AA 91-121) (ABIN5647192)

Target

See all MC3R Antibodies
MC3R (Melanocortin 3 Receptor (MC3R))

Reactivity

  • 42
  • 39
  • 27
  • 4
Human, Mouse

Host

  • 61
  • 1
  • 1
Rabbit

Clonality

  • 63
Polyclonal

Conjugate

  • 20
  • 6
  • 5
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This MC3R antibody is un-conjugated

Application

  • 44
  • 25
  • 13
  • 13
  • 6
  • 4
  • 3
  • 3
  • 3
  • 1
  • 1
Western Blotting (WB)
  • Binding Specificity

    • 15
    • 8
    • 7
    • 6
    • 5
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 91-121

    Purification

    Antigen affinity purified

    Immunogen

    Amino acids 91-121 (NALETIMIAIVHSDYLTFEDQFIQHMDNIFD) from the human protein were used as the immunogen for the MC3 Receptor antibody.

    Isotype

    IgG
  • Application Notes

    Optimal dilution of the MC3 Receptor antibody should be determined by the researcher.\. WB: 0.5-1 μg/mL

    Restrictions

    For Research Use only
  • Buffer

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

    Storage

    -20 °C

    Storage Comment

    After reconstitution, the MC3 Receptor antibody can be stored for up to one month at 4°C. For long-term, aliquot and store at -20°C. Avoid repeated freezing and thawing.
  • Target

    MC3R (Melanocortin 3 Receptor (MC3R))

    Alternative Name

    MC3R / MC3 Receptor

    Background

    Melanocortin receptor 3 is a protein that in humans is encoded by the MC3R gene. It is mapped to 20q13.2. This gene encodes a G-protein-coupled receptor for melanocyte-stimulating hormone and adrenocorticotropic hormone that is expressed in tissues other than the adrenal cortex and melanocytes. This gene maps to the same region as the locus for benign neonatal epilepsy. Mice deficient for this gene have increased fat mass despite decreased food intake, suggesting a role for this gene product in the regulation of energy homeostasis. Mutations in this gene are associated with a susceptibility to obesity in humans.

    UniProt

    P41968

    Pathways

    cAMP Metabolic Process
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