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CCR7 Protein

MNP Membrane Nanoparticle CCR7-Protein exprimiert in HEK-293 Cells.
Produktnummer ABIN7597218

Kurzübersicht für CCR7 Protein (ABIN7597218)

Target

Alle CCR7 Proteine anzeigen
CCR7 (Chemokine (C-C Motif) Receptor 7 (CCR7))

Protein-Typ

MNP Membrane Nanoparticle

Spezies

  • 10
  • 2
  • 1
Human

Quelle

  • 5
  • 5
  • 1
HEK-293 Cells
  • Verwendungszweck

    Human CCR7 full length protein-MNP
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  • Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Lyophilized

    Buffer

    Lyophilized from PBS. Normally 5% – 8% trehalose is added as protectants before lyophilization.

    Lagerung

    -20 °C,-80 °C

    Informationen zur Lagerung

    Store at -20°C to -80°C for 12 months in lyophilized form. After reconstitution, if not intended for use within a month, aliquot and store at -80°C (Avoid repeated freezing and thawing). Lyophilized proteins are shipped at ambient temperature.

    Haltbarkeit

    12 months
  • Target

    CCR7 (Chemokine (C-C Motif) Receptor 7 (CCR7))

    Andere Bezeichnung

    CCR7

    Hintergrund

    BLR2, CC-CKR-7, CCR-7, CD197, CDw197, CMKBR7, EBI1
    The protein is a member of the G protein-coupled receptor family. This receptor was identified as a gene induced by the Epstein-Barr virus (EBV), and is thought to be a mediator of EBV effects on B lymphocytes. This receptor is expressed in various lymphoid tissues and activates B and T lymphocytes. It has been shown to control the migration of memory T cells to inflamed tissues, as well as stimulate dendritic cell maturation. The chemokine (C-C motif) ligand 19 (CCL19/ECL) has been reported to be a specific ligand of this receptor. Signals mediated by this receptor regulate T cell homeostasis in lymph nodes, and may also function in the activation and polarization of T cells, and in chronic inflammation pathogenesis.

    Molekulargewicht

    The human full length CCR7 protein has a MW of 42.9 kDa

    UniProt

    P32248

    Pathways

    Regulation of Actin Filament Polymerization, Positive Regulation of Immune Effector Process
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