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FOXP3 Antikörper

Dieses Anti-FOXP3-Antikörper ist ein Ratte Polyklonal-Antikörper zur Detektion von FOXP3 in WB und ELISA. Geeignet für Maus.
Produktnummer ABIN1169337

Kurzübersicht für FOXP3 Antikörper (ABIN1169337)

Target

Alle FOXP3 Antikörper anzeigen
FOXP3 (Forkhead Box P3 (FOXP3))

Reaktivität

  • 172
  • 144
  • 66
  • 28
  • 7
  • 3
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Maus

Wirt

  • 121
  • 82
  • 19
  • 2
Ratte

Klonalität

  • 118
  • 106
Polyklonal

Konjugat

  • 113
  • 15
  • 12
  • 10
  • 8
  • 4
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
Dieser FOXP3 Antikörper ist unkonjugiert

Applikation

  • 138
  • 94
  • 65
  • 53
  • 42
  • 37
  • 30
  • 29
  • 27
  • 18
  • 10
  • 8
  • 7
  • 6
  • 4
  • 3
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
Western Blotting (WB), ELISA
  • Spezifität

    Recognizes mouse FOXP3. Detects a band of ~46-49 kDa by Western blot.

    Kreuzreaktivität

    Maus

    Sterilität

    0.2 μm filtered

    Immunogen

    Recombinant mouse FOXP3.
  • Applikationshinweise

    Optimal working dilution should be determined by the investigator.

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Liquid

    Konzentration

    Lot specific

    Buffer

    0.2μm-filtered solution in PBS, pH 7.4. Contains no preservatives.

    Konservierungsmittel

    Without preservative

    Lagerung

    4 °C,-20 °C

    Informationen zur Lagerung

    Short Term Storage: +4°C
    Long Term Storage: -20°C
    Stable for at least 6 months after receipt when stored at -20°C.

    Haltbarkeit

    6 months
  • Target

    FOXP3 (Forkhead Box P3 (FOXP3))

    Andere Bezeichnung

    FOXP3

    Hintergrund

    FOXP3 is involved in immune system responses. It functions as the master regulator in the development and function of regulatory T cells. FOX proteins belong to the forkhead/winged-helix family of transcriptional regulators and are presumed to exert control via similar DNA binding interactions during transcription. Defects in FOXP3 are the cause of immunodeficiency polyendocrinopathy, enteropathy, X-linked syndrome (IPEX), also known as X-linked autoimmunity-immunodeficiency syndrome. IPEX is characterized by neonatal onset insulin-dependent diabetes mellitus, infections, secretory diarrhea, trombocytopenia, anemia and eczema.

    UniProt

    Q99JB6

    Pathways

    Chromatin Binding, Regulation of Leukocyte Mediated Immunity, Positive Regulation of Immune Effector Process, Production of Molecular Mediator of Immune Response, Activated T Cell Proliferation
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