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HFE antibody

HFE Reactivity: Human WB Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN5647142
  • Target See all HFE Antibodies
    HFE (Hemochromatosis (HFE))
    Reactivity
    • 48
    • 9
    • 8
    • 6
    • 6
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    Human
    Host
    • 43
    • 6
    Rabbit
    Clonality
    • 44
    • 5
    Polyclonal
    Conjugate
    • 26
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This HFE antibody is un-conjugated
    Application
    • 43
    • 20
    • 15
    • 13
    • 13
    • 6
    • 5
    • 3
    • 3
    • 3
    • 1
    • 1
    Western Blotting (WB)
    Purification
    Antigen affinity purified
    Immunogen
    Amino acids Q82-R199 from the human protein were used as the immunogen for the HFE antibody.
    Isotype
    IgG
    Top Product
    Discover our top product HFE Primary Antibody
  • Application Notes
    Optimal dilution of the HFE 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 HFE 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
    HFE (Hemochromatosis (HFE))
    Alternative Name
    HFE (Hereditary hemochromatosis protein) (HFE Products)
    Synonyms
    HFE1 antibody, HH antibody, HLA-H antibody, MVCD7 antibody, TFQTL2 antibody, MR2 antibody, hemochromatosis antibody, HFE antibody, Hfe antibody
    Background
    Human hemochromatosis protein, also known as HFE, is a protein which in humans is encoded by the HFE gene. The gene is located on short arm of chromosome 6 at location 6p21.3. It is a membrane protein that is similar to MHC class I-type proteins and associates with beta2-microglobulin (beta2M). It is thought that this protein functions to regulate iron absorption by regulating the interaction of the transferrin receptor with transferrin. The iron storage disorder, hereditary haemochromatosis, is a recessive genetic disorder that results from defects in this gene.
    UniProt
    Q30201
    Pathways
    Transition Metal Ion Homeostasis, Regulation of Leukocyte Mediated Immunity, Positive Regulation of Immune Effector Process
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