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BEBOV GP Protein (AA 33-304) (His tag)

BEBOV GP Origine: Ebola Virus Hôte: HEK-293 Cells Recombinant >95 %
N° du produit ABIN6941976
  • Antigène Tous les produits BEBOV GP
    BEBOV GP (Bundibugyo Ebola Virus Envelope Glycoprotein (BEBOV GP))
    Type de proteíne
    Recombinant
    Attributs du protein
    AA 33-304
    Origine
    Ebola Virus
    Source
    • 2
    • 1
    HEK-293 Cells
    Purification/Conjugué
    Cette BEBOV GP protéine est marqué à la His tag.
    Fonction
    Recombinant Ebolavirus (subtype Bundibugyo,strain Uganda 2007) Envelope Glycoprotein 1 (GP1) protein produced in HEK293 cells. Protein contains a C-terminal 6x His-tag
    Specificité
    Ebola virus envelope glycoprotein (GP1) is derived from the GP1 sequence (Accession # ACI28624), expressing Ile33 – Gln304.This Ebola virus envelope glycoprotein (GP1) is fused with a polyhistidine tag at the C-terminus, and has a calculated MW of 31.8 kDa. The protein is expressed in HEK293 cells.
    Attributs du produit
    Ebola Virus Envelope Glycoprotein (GP1) (Bundibugyo)
    Pureté
    >95 %
  • Commentaires

    This Ebola virus envelope glycoprotein (GP1) is derived from the GP1 sequence (Accession # ACI28624), expressing Ile33 – Gln304.This Ebola virus envelope glycoprotein (GP1) is fused with a polyhistidine tag at the C-terminus, and has a calculated MW of 31.8 kDa. The protein is expressed in HEK293 cells. DTT-reduced Protein migrates as 40-60 kDa in SDS-PAGE.

    Restrictions
    For Research Use only
  • Format
    Lyophilized
    Buffer
    PBS pH 7.4
    Stock
    4 °C
    Stockage commentaire
    4°C
  • Antigène
    BEBOV GP (Bundibugyo Ebola Virus Envelope Glycoprotein (BEBOV GP))
    Autre désignation
    Ebola Envelope Glycoprotein (GP1) (Bundibugyo) (BEBOV GP Produits)
    Classe de substances
    Viral Protein
    Sujet
    Ebola virus envelope glycoprotein is initially produced as a precursor known as pre-GP, which is cleaved by furin into two subunits, GP1 and GP2, which remain associated through a disulfide linkage between Cys53 of GP1 and Cys609 of GP2. This heterodimer assembles into a 450-kDa trimer at the surface of nascent virions. The virion-attached GP is critical in the EBOV life cycle, as it is solely responsible for attachment, fusion and entry of target cells. Moreover, GP is responsible for critical pathogenic differences among viral species.
    Ebola hemorrhagic fever (EHF) is a severe disease caused by several species of Ebolavirus (EBOV), in the family Filoviridae. Prior to 2007, four species of EBOV had been identified, with two (Zaire ebolavirus andSudan ebolavirus) having caused significant disease outbreaks in humans. Outbreaks of EHF are associated with person-to-person transmission after the virus is introduced into humans from a zoonotic reservoir. During outbreaks the virus is commonly transmitted through direct contact with infected persons or their bodily fluids. The onset of EHF is associated with nonspecific signs and symptoms, including fever, myalgias, headache, abdominal pain, nausea, vomiting, and diarrhoea. In the later stages of disease, overt hemorrhage has been reported in up to 50% of cases.
    The presence of a fifth EBOV virus species,Bundibugyo ebolavirus (BEBOV) was identified after an outbreak of EHF in the Bundibugyo District of western Uganda in 2007.
    UniProt
    ACI28624
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