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Transferrin Receptor 2 Antikörper

Dieses Maus Monoklonal-Antikörper erkennt spezifisch Transferrin Receptor 2 in WB, IF und FACS. Er zeigt eine Reaktivität gegenüber Human, Maus, Ratte und Affe.
Produktnummer ABIN2733490

Kurzübersicht für Transferrin Receptor 2 Antikörper (ABIN2733490)

Target

Alle Transferrin Receptor 2 (TFR2) Antikörper anzeigen
Transferrin Receptor 2 (TFR2)

Reaktivität

  • 37
  • 14
  • 9
  • 3
  • 3
  • 2
  • 2
  • 2
  • 2
  • 1
Human, Maus, Ratte, Affe

Wirt

  • 47
  • 9
Maus

Klonalität

  • 38
  • 18
Monoklonal

Konjugat

  • 37
  • 9
  • 3
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Dieser Transferrin Receptor 2 Antikörper ist unkonjugiert

Applikation

  • 44
  • 39
  • 27
  • 21
  • 7
  • 6
  • 3
  • 3
  • 2
  • 1
  • 1
Western Blotting (WB), Immunofluorescence (IF), Flow Cytometry (FACS)

Klon

2B4
  • Produktmerkmale

    Homo sapiens transferrin receptor 2 (TFR2), transcript variant 1

    Aufreinigung

    Purified from mouse ascites fluids by affinity chromatography

    Immunogen

    Full length human recombinant protein of human TFR2(NP_003218) produced in HEK293T cell.

    Isotyp

    IgG2a
  • Applikationshinweise

    WB 1:500~2000, IF 1:100, FLOW 1:100,

    Kommentare

    The concentration of the product may vary between diferrent lots.

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Liquid

    Konzentration

    0.5-1.0 mg/mL

    Buffer

    PBS (PH 7.3) containing 1 % BSA, 50 % glycerol and 0.02 % sodium azide.

    Konservierungsmittel

    Sodium azide

    Vorsichtsmaßnahmen

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

    Lagerung

    -20 °C
  • Target

    Transferrin Receptor 2 (TFR2)

    Andere Bezeichnung

    TFR2

    Hintergrund

    This gene encodes a single-pass type II membrane protein, which is a member of the transferrin receptor-like family. This protein mediates cellular uptake of transferrin-bound iron, and may be involved in iron metabolism, hepatocyte function and erythrocyte differentiation. Mutations in this gene have been associated with hereditary hemochromatosis type III. Alternatively spliced transcript variants encoding different isoforms have been described for this gene.

    Molekulargewicht

    88.6 kDa

    Gen-ID

    7036

    NCBI Accession

    NM_003227

    HGNC

    7036

    Pathways

    Transition Metal Ion Homeostasis
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