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IL-17 Kit ELISA

Kit ELISA Humain IL-17, test Colorimetric pour la quantification de Humain IL-17.
N° du produit ABIN4986934

Aperçu rapide pour IL-17 Kit ELISA (ABIN4986934)

Antigène

Voir toutes IL-17 (IL17) Kits ELISA
IL-17 (IL17) (Interleukin 17 (IL17))

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Humain

Méthode de détection

Colorimetric

Type de méthode

Sandwich ELISA

Gamme de detection

15.625-1000 pg/mL

Application

ELISA

Type d'échantillon

Cell Culture Supernatant, Serum, Plasma (heparin), Plasma (citrate), Plasma (EDTA)
  • Seuil minimal de détection

    15.625 pg/mL

    Analytical Method

    Quantitative

    Specificité

    Natural and recombinant Human IL-17 Ligand

    Sensibilité

    7 pg/mL

    Matériel non inclus

    • Microplate reader.
    • Pipettes and pipette tips.
    • EP tube Deionized or distilled water.
  • Indications d'application

    Detection Wavelength: 450 nm

    Volume d'échantillon

    20 μL

    Durée du test

    3 h

    Plaque

    Pre-coated

    Restrictions

    For Research Use only
  • Stock

    4 °C
  • Antigène Voir toutes IL-17 (IL17) Kits ELISA

    IL-17 (IL17) (Interleukin 17 (IL17))

    Autre désignation

    IL-17

    Sujet

    IL-17, originally identified as mouse cytotoxic T lymphocyte-associated antigen-8 (CTLA-8) (1), is produced by activated T lymphocytes, primarily by memory T cells (1-4). IL-17 appears to mediate communication between the immune system and the hematopoietic system.IL-17 is a disulfide-linked homodimer (2, 4). Each polypeptide has 155 amino acid (aa) residues (predicted mass = 17.5 kDa), including a 19 aa residue hydrophobic leader sequence (2). There are six cysteines plus one potential N-linked glycosylation site, which is variably glycosylated, at least with recombinant proteins (2, 4). The aa sequence of human IL-17 is 63 % and 58 % identical to mouse and rat IL-17 and 72 % identical to the thirteenth ORF of Herpesvirus saimiri (2, 4). There is at least some species specificity for in vitro action on bone-marrow stromal cells (3).IL-17 mediation of T cell communication with the hematopoietic system is suggested by two observations. T cell-derived IL-17 induces fibroblasts to produce IL-6, IL-8, ICAM-1 and G-CSF, apparently by an NF-?B-mediated mechanism (5). IL-6 in turn promotes development of granulocyte/macrophage colonies, and G-CSF directs development of neutrophils (4, 6-9). IL-17 also enhances proliferation of partially activated T cells (5) and upregulates nitric oxide (NO) production in osteoarthritic cartilage (10).
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