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RAGE antibody

AGER Reactivity: Human WB Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN289974
  • Target See all RAGE (AGER) Antibodies
    RAGE (AGER) (Advanced Glycosylation End Product-Specific Receptor (AGER))
    Reactivity
    • 148
    • 82
    • 64
    • 8
    • 6
    • 5
    • 4
    • 3
    • 2
    • 2
    • 1
    Human
    Host
    • 142
    • 11
    • 4
    • 2
    • 1
    Rabbit
    Clonality
    • 136
    • 23
    • 1
    Polyclonal
    Conjugate
    • 71
    • 12
    • 11
    • 10
    • 9
    • 6
    • 3
    • 3
    • 3
    • 3
    • 3
    • 3
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    This RAGE antibody is un-conjugated
    Application
    • 127
    • 71
    • 54
    • 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.
    Immunogen
    Partial peptide of Human RAGE
    Top Product
    Discover our top product AGER Primary Antibody
  • 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)
    Preservative
    ProClin
    Storage
    -20 °C
  • Target
    RAGE (AGER) (Advanced Glycosylation End Product-Specific Receptor (AGER))
    Alternative Name
    RAGE (AGER Products)
    Synonyms
    RAGE antibody, AGER antibody, advanced glycosylation end-product specific receptor antibody, advanced glycosylation end product-specific receptor antibody, MAPK/MAK/MRK overlapping kinase antibody, AGER antibody, Ager antibody, LOC719012 antibody
    Background
    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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