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HFE antibody

This Rabbit Polyclonal antibody specifically detects HFE in WB. It exhibits reactivity toward Human.
Catalog No. ABIN499087

Quick Overview for HFE antibody (ABIN499087)

Target

See all HFE Antibodies
HFE (Hemochromatosis (HFE))

Reactivity

  • 54
  • 9
  • 7
  • 5
  • 5
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
Human

Host

  • 50
  • 6
Rabbit

Clonality

  • 50
  • 6
Polyclonal

Conjugate

  • 28
  • 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

  • 44
  • 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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