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HFE Antikörper

Dieser 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

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

Wirt

  • 49
  • 6
Kaninchen

Klonalität

  • 50
  • 5
Polyklonal

Konjugat

  • 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
Dieser HFE Antikörper ist unkonjugiert

Applikation

  • 43
  • 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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