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Endoglin antibody

ENG Reactivity: Human WB, FACS, IHC, ELISA, IF Host: Mouse Monoclonal 3A9 unconjugated
Catalog No. ABIN865407
  • Target See all Endoglin (ENG) Antibodies
    Endoglin (ENG)
    Reactivity
    • 162
    • 63
    • 42
    • 17
    • 10
    • 6
    • 5
    • 3
    • 3
    • 3
    • 1
    Human
    Host
    • 101
    • 85
    • 16
    • 1
    Mouse
    Clonality
    • 103
    • 99
    • 1
    Monoclonal
    Conjugate
    • 94
    • 24
    • 22
    • 22
    • 13
    • 7
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This Endoglin antibody is un-conjugated
    Application
    • 134
    • 122
    • 55
    • 49
    • 33
    • 18
    • 16
    • 14
    • 14
    • 13
    • 13
    • 7
    • 6
    • 5
    • 4
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    Western Blotting (WB), Flow Cytometry (FACS), Immunohistochemistry (IHC), ELISA, Immunofluorescence (IF)
    Purification
    Ascitic fluid
    Immunogen
    Purified recombinant fragment of human CD105 expressed in E. Coli.
    Clone
    3A9
    Isotype
    IgG1
    Top Product
    Discover our top product ENG Primary Antibody
  • Application Notes
    WB: 1/500 - 1/2000, IHC: 1/200 - 1/1000, IF: 1/200 - 1/1000, FC: 1/200 - 1/400, ELISA: Propose dilution 1/10000.
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    100g/100l
    Preservative
    Sodium azide
    Precaution of Use
    This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Storage
    4 °C
  • Target
    Endoglin (ENG)
    Alternative Name
    CD105 (ENG Products)
    Background
    This gene encodes a homodimeric transmembrane protein which is a major glycoprotein of the vascular endothelium. This protein is a component of the transforming growth factor beta receptor complex and it binds TGFB1 and TGFB3 with high affinity. Mutations in this gene cause hereditary hemorrhagic telangiectasia, also known as Osler-Rendu-Weber syndrome 1, an autosomal dominant multisystemic vascular dysplasia. Synonyms: ENG, END, ORW, HHT1, ORW1, CD105, FLJ41744
    Molecular Weight
    71kDa
    Gene ID
    2022
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