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HFE antibody

This Rabbit Polyclonal antibody specifically detects HFE in WB. It exhibits reactivity toward Human.
Catalog No. ABIN499087
$666.00
Plus shipping costs $50.00
0.1 mg
Shipping to: United States
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Quick Overview for HFE antibody (ABIN499087)

Target

See all HFE Antibodies
HFE (Hemochromatosis (HFE))

Reactivity

  • 53
  • 9
  • 7
  • 5
  • 5
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
Human

Host

  • 49
  • 6
Rabbit

Clonality

  • 50
  • 5
Polyclonal

Conjugate

  • 27
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 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
  • 5
  • 5
  • 5
  • 3
  • 3
  • 1
  • 1
Western Blotting (WB)
  • Specificity

    This antibody detects endogenous levels of HLA-H protein. (region surrounding Ile104)

    Cross-Reactivity (Details)

    Species reactivity (tested):Human.

    Purification

    Affinity chromatography using epitope-specific immunogen

    Purity

    > 95 % pure by SDS-PAGE
  • Application Notes

    Western blot: 1: 500 - 1: 1000.
    Other applications not tested.
    Optimal dilutions are dependent on conditions and should be determined by the user.

    Restrictions

    For Research Use only
  • Concentration

    1.0 mg/mL

    Buffer

    Phosphate buffered saline (PBS), pH 7.2, 0.05 % 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.

    Handling Advice

    Avoid repeated freezing and thawing.

    Storage

    4 °C/-20 °C

    Storage Comment

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

    HFE (Hemochromatosis (HFE))

    Alternative Name

    HFE / HLAH

    Background

    The protein encoded by this gene 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. At least nine alternatively spliced variants have been described for this gene. Additional variants have been found but their full-length nature has not been determined.Synonyms: Hereditary hemochromatosis protein

    Molecular Weight

    approx. 40 kDa

    Gene ID

    3077

    NCBI Accession

    NP_000401

    UniProt

    Q30201

    Pathways

    Transition Metal Ion Homeostasis, Regulation of Leukocyte Mediated Immunity, Positive Regulation of Immune Effector Process
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