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HFE Antikörper

Dieses Kaninchen Polyklonal-Antikörper erkennt spezifisch HFE in WB. Er zeigt eine Reaktivität gegenüber Human.
Produktnummer ABIN499087

Kurzübersicht für HFE Antikörper (ABIN499087)

Target

Alle HFE Antikörper anzeigen
HFE (Hemochromatosis (HFE))

Reaktivität

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

Wirt

  • 50
  • 6
Kaninchen

Klonalität

  • 50
  • 6
Polyklonal

Konjugat

  • 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
Dieser HFE Antikörper ist unkonjugiert

Applikation

  • 44
  • 20
  • 15
  • 13
  • 13
  • 5
  • 5
  • 5
  • 3
  • 3
  • 1
  • 1
Western Blotting (WB)
  • Spezifität

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

    Kreuzreaktivität (Details)

    Species reactivity (tested):Human.

    Aufreinigung

    Affinity chromatography using epitope-specific immunogen

    Reinheit

    > 95 % pure by SDS-PAGE
  • Applikationshinweise

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

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Konzentration

    1.0 mg/mL

    Buffer

    Phosphate buffered saline (PBS), pH 7.2, 0.05 % Sodium Azide

    Konservierungsmittel

    Sodium azide

    Vorsichtsmaßnahmen

    This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Handhabung

    Avoid repeated freezing and thawing.

    Lagerung

    4 °C/-20 °C

    Informationen zur Lagerung

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

    HFE (Hemochromatosis (HFE))

    Andere Bezeichnung

    HFE / HLAH

    Hintergrund

    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

    Molekulargewicht

    approx. 40 kDa

    Gen-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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