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IFNA ELISA Kit

IFNA Reaktivität: Human Colorimetric Sandwich ELISA 15.625-1000 pg/mL Cell Culture Supernatant, Plasma (EDTA), Plasma (citrate), Plasma (heparin), Serum
Produktnummer ABIN4986917
  • Target Alle IFNA ELISA Kits anzeigen
    IFNA (Interferon alpha (IFNA))
    Reaktivität
    • 5
    • 5
    • 4
    • 3
    • 3
    • 3
    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    Human
    Nachweismethode
    Colorimetric
    Methodentyp
    Sandwich ELISA
    Detektionsbereich
    15.625-1000 pg/mL
    Untere Nachweisgrenze
    15.625 pg/mL
    Applikation
    ELISA
    Proben
    Cell Culture Supernatant, Serum, Plasma (heparin), Plasma (citrate), Plasma (EDTA)
    Analytische Methode
    Quantitative
    Spezifität
    Natural and recombinant Human IFN-α Ligand
    Sensitivität
    7 pg/mL
    Benötigtes Material
    • Microplate reader.
    • Pipettes and pipette tips.
    • EP tube Deionized or distilled water.
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  • Applikationshinweise
    Detection Wavelength: 450 nm
    Probenmenge
    20 μL
    Testdauer
    3 h
    Plattentyp
    Pre-coated
    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Lagerung
    4 °C
  • Target Alle IFNA ELISA Kits anzeigen
    IFNA (Interferon alpha (IFNA))
    Andere Bezeichnung
    IFN-alpha (IFNA Produkte)
    Synonyme
    IFN-alphaO ELISA Kit, IFN-ALPHA-1 ELISA Kit, IFN1@ ELISA Kit, Ifa ELISA Kit, Ifa8 ELISA Kit, interferon alpha 16 ELISA Kit, interferon, alpha 1 ELISA Kit, interferon alpha ELISA Kit, interferon-alpha ELISA Kit, IFNA16 ELISA Kit, IFNA1 ELISA Kit, Ifna ELISA Kit, IFNA ELISA Kit
    Hintergrund
    IFN-α/β R2, also known as IFNAR2, is a 100 kDa glycoprotein in the class II cytokine receptor family. These proteins form heterodimeric receptor complexes that transduce signals from the interferon, IL 10, and IL28 families of cytokines (1, 2). IFN-α/β R2, in association with IFN-α/β R1, is required for mediating the antiviral,antiproliferative, and apoptotic effects of the type I interferons IFN-α and IFN-β.IFN-α/β R2 is the principal ligand binding subunit of the receptor. Ligand binding is stabilized by the subsequent association with IFN-α/β R1, resulting in the formation of a signaling ternary receptor complex (3, 4). Mature human IFN-α/β R2 consists of a 217 amino acid (aa) extracellular domain (ECD) with two fibronectin type III repeats, a 21 aa transmembrane segment, and a 251 aa cytoplasmic domain. Alternate splicing generates a secreted isoform that corresponds to the ECD and a 50 kDa transmembrane isoform with a substituted and truncated cytoplasmic region (5, 6). The short isoform is impaired in its ability to activate signaling molecules and functions as a dominant negative receptor subunit (7 9). IFN-α/β R2 is also subject to presenilin dependent intramembrane proteolysis, resulting in the liberation of nearly the entire ECD as well as the cytoplasmic domain which migrates to the nucleus and can inhibit gene transcription (10). High concentrations of soluble IFN-α/β R2 bind and neutralize IFN-α and IFN-β, while lower concentrations prolong the antiviral activity of circulating IFN-β but not IFN-α (11). Human but not mouse IFN-α/β R2 constitutively associates with STAT4, which may account for species specific differences observed in type I interferon responses (12). Within the ECD, human IFN-α/β R2 shares 63 % , 60 %, and 48 % aa sequence identity with bovine, mouse, and ovine IFN-α/β R2, respectively.
    Pathways
    JAK-STAT Signalweg, TLR Signalweg, Hepatitis C, Inflammasome
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