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Fibulin 5 Antikörper

FBLN5 Reaktivität: Human, Maus, Ratte ELISA, IHC Wirt: Kaninchen Polyclonal unconjugated
Produktnummer ABIN2425853
  • Target Alle Fibulin 5 (FBLN5) Antikörper anzeigen
    Fibulin 5 (FBLN5)
    Reaktivität
    • 53
    • 30
    • 23
    • 1
    Human, Maus, Ratte
    Wirt
    • 52
    • 6
    • 1
    Kaninchen
    Klonalität
    • 53
    • 8
    Polyklonal
    Konjugat
    • 28
    • 8
    • 6
    • 4
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Dieser Fibulin 5 Antikörper ist unkonjugiert
    Applikation
    • 56
    • 32
    • 15
    • 5
    • 4
    • 3
    • 3
    • 1
    ELISA, Immunohistochemistry (IHC)
    Aufreinigung
    Affinity purification
    Immunogen
    Synthetic peptide of human FBLN5
    Isotyp
    IgG
    Top Product
    Discover our top product FBLN5 Primärantikörper
  • Applikationshinweise
    IHC 1:50-1:200
    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Format
    Liquid
    Konzentration
    1.2 mg/mL
    Buffer
    PBS with 0.05 % sodium azide and 50 % glycerol, PH7.4
    Konservierungsmittel
    Sodium azide
    Handhabung
    Avoid freeze / thaw cycles.
    Lagerung
    -20 °C
    Informationen zur Lagerung
    Store at -20°C. Avoid freeze / thaw cycles.
  • Target
    Fibulin 5 (FBLN5)
    Andere Bezeichnung
    Fibulin 5 (FBLN5 Produkte)
    Synonyme
    zgc:103575 antikoerper, FBLN5 antikoerper, MGC108414 antikoerper, Fibulin-5 antikoerper, DKFZp469K0327 antikoerper, ADCL2 antikoerper, ARCL1A antikoerper, ARMD3 antikoerper, DANCE antikoerper, EVEC antikoerper, FIBL-5 antikoerper, UP50 antikoerper, A55 antikoerper, fibulin 5 antikoerper, fbln5 antikoerper, FBLN5 antikoerper, Fbln5 antikoerper
    Hintergrund
    The protein encoded by this gene is a secreted, extracellular matrix protein containing an Arg-Gly-Asp (RGD) motif and calcium-binding EGF-like domains. It promotes adhesion of endothelial cells through interaction of integrins and the RGD motif. It is prominently expressed in developing arteries but less so in adult vessels. However, its expression is reinduced in balloon-injured vessels and atherosclerotic lesions, notably in intimal vascular smooth muscle cells and endothelial cells. Therefore, the protein encoded by this gene may play a role in vascular development and remodeling. Defects in this gene are a cause of autosomal dominant cutis laxa, autosomal recessive cutis laxa type I (CL type I), and age-related macular degeneration type 3 (ARMD3).
    NCBI Accession
    NP_006320
    Pathways
    SARS-CoV-2 Protein Interaktom
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