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Endoglin Protein (ENG) (TRX tag,His tag)

ENG Origin: Human Host: Escherichia coli (E. coli) Recombinant > 95 % as determined by reducing SDS-PAGE.
Catalog No. ABIN7318427
  • Target See all Endoglin (ENG) Proteins
    Endoglin (ENG)
    Protein Type
    Recombinant
    Origin
    • 18
    • 7
    • 2
    • 2
    Human
    Source
    • 13
    • 8
    • 6
    • 2
    Escherichia coli (E. coli)
    Purification tag / Conjugate
    This Endoglin protein is labelled with TRX tag,His tag.
    Purpose
    Recombinant Human Endoglin/CD105 Protein (His&Trx Tag)
    Sequence
    Glu26-Gln176
    Characteristics
    Recombinant Human Endoglin is produced by our E.coli expression system and the target gene encoding Glu26-Gln176 is expressed with a Trx, 6His tag at the N-terminus.
    Purity
    > 95 % as determined by reducing SDS-PAGE.
    Endotoxin Level
    < 1.0 EU per μg as determined by the LAL method.
    Top Product
    Discover our top product ENG Protein
  • Restrictions
    For Research Use only
  • Format
    Frozen, Liquid
    Buffer
    Supplied as a 0.2 μm filtered solution of 20 mM PB,150 mM NaCl, pH 7.4.
    Storage
    -20 °C
    Storage Comment
    Store at < -20°C, stable for 6 months. Please minimize freeze-thaw cycles.
  • Target
    Endoglin (ENG)
    Alternative Name
    Endoglin/CD105 (ENG Products)
    Synonyms
    ENG Protein, MGC137842 Protein, DKFZp469D0419 Protein, END Protein, HHT1 Protein, ORW1 Protein, AI528660 Protein, AI662476 Protein, CD105 Protein, S-endoglin Protein, endoglin Protein, ENG Protein, Eng Protein
    Background

    Background: Endoglin is a single-pass type I membrane protein which restricted to endothelial cells in all tissues except bone marrow. Endoglin as major glycoprotein of vascular endothelium, it has been found on endothelial cells, activated macrophages, fibroblasts, and smooth muscle cells. Furthermore, Homodimer forms a heteromeric complex with the signaling receptors for transforming growth factor-beta: TGFBR1 and/or TGFBR2. It may have an important role in the binding of endothelial cells to integrins and/or other RGD receptors. Defects in ENG are the cause of hereditary hemorrhagic telangiectasia type 1 (HHT1), which is an autosomal dominant multisystemic vascular dysplasia, characterized by recurrent epistaxis, muco-cutaneous telangiectases, gastro-intestinal hemorrhage, and pulmonary (PAVM), cerebral (CAVM) and hepatic arteriovenous malformations.

    Synonym: Endoglin, END, CD105, ENG,HHT1,ORW1

    Molecular Weight
    33.6 kDa
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