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RAGE anticorps

AGER Reactivité: Humain WB Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN289974
  • Antigène Voir toutes RAGE (AGER) Anticorps
    RAGE (AGER) (Advanced Glycosylation End Product-Specific Receptor (AGER))
    Reactivité
    • 143
    • 82
    • 64
    • 8
    • 6
    • 5
    • 4
    • 3
    • 2
    • 2
    • 1
    Humain
    Hôte
    • 137
    • 11
    • 4
    • 2
    • 1
    Lapin
    Clonalité
    • 131
    • 23
    • 1
    Polyclonal
    Conjugué
    • 71
    • 11
    • 10
    • 9
    • 8
    • 5
    • 3
    • 3
    • 3
    • 3
    • 3
    • 3
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    Cet anticorp RAGE est non-conjugé
    Application
    • 127
    • 66
    • 49
    • 34
    • 27
    • 26
    • 24
    • 11
    • 8
    • 8
    • 7
    • 3
    • 2
    • 1
    • 1
    • 1
    Western Blotting (WB)
    Purification
    This antibody was purified from rabbit serum by Protein G affinity chromatography.
    Immunogène
    Partial peptide of Human RAGE
    Top Product
    Discover our top product AGER Anticorps primaire
  • Restrictions
    For Research Use only
  • Concentration
    0.25 mg/ml
    Buffer
    PBS (containing 2% Block Ace as a stabilizer, 0.1% Proclin as a bacteriostat)
    Agent conservateur
    ProClin
    Stock
    -20 °C
  • Antigène
    RAGE (AGER) (Advanced Glycosylation End Product-Specific Receptor (AGER))
    Autre désignation
    RAGE (AGER Produits)
    Synonymes
    anticorps RAGE, anticorps AGER, anticorps advanced glycosylation end-product specific receptor, anticorps advanced glycosylation end product-specific receptor, anticorps MAPK/MAK/MRK overlapping kinase, anticorps AGER, anticorps Ager, anticorps LOC719012
    Sujet
    RAGE is the receptor of AGEs, advanced glycation end products with 35,000 molecularweight and was cloned from bovine lung in 1992 ( David Stern et al.,). RAGE has been foundin several tissues such as monocytes, macrophages, endothelial cells, astocytes. The ligand ofRAGE is demonstrated not only AGEs but also anfoterin, EN-RAGE,N-carboxymethyllysine(CML),beta-amyloid and so on. The accumulation of AGEs-proteins invivo has been demonstrated in several disease, it is not clear whether AGEs-proteinsaccumulated in vivo is a direct cause of the disease or rather reflects its effect. Regarding this issue, AGEs-modified proteins are known to interact with several cells by the AGEs-receptors and induce several cellular phenomena. Recently, it has been discovered that RAGE isinvolved in pathophysiological function of diabetes and Alzheimer
    Pathways
    Carbohydrate Homeostasis, Toll-Like Receptors Cascades, Smooth Muscle Cell Migration, S100 Proteins
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