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Recombinant EBOV GP, CF 100 UG

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產(chǎn)品介紹

    基本參數(shù)

    詳細(xì)說(shuō)明

    • Purity

      >95%, by SDS-PAGE visualized with Silver Staining and quantitative densitometry by Coomassie? Blue Staining.

    • Endotoxin Level

      <0.10 EU per 1 μg of the protein by the LAL method.  

    • Activity

      Measured by its binding ability in a functional ELISA. When Recombinant Viral EBOV GP is immobilized at 2 μg/mL (100 μL/well), the concentration of Recombinant Human CLEC10A/CD301 (Catalog # ) that produces 50% of the optimal binding response is approximately 20-100 ng/mL.

    • Source

      Chinese Hamster Ovary cell line, CHO-derived

      Z. ebolavirus GP1
      (Ile33-Arg501)
      Accession # Q05320

      Z. ebolavirus GP2
      (Glu502-Gln650)
      Accession # Q05320
      HHHHHH
      N-terminusC-terminus
    • N-terminal Sequence    
      Analysis

      Ile33 (GP1) & Glu502 (GP2)

    • Structure / Form

      Disulfide-linked heterodimer

    • Predicted Molecular Mass

      69 kDa

    • SDS-PAGE

      17-24 kDa and 105-120 kDa, reducing conditions

    9016-EB

     

    Formulation Lyophilized from a 0.2 μm filtered solution in Tris and NaCl.


    Reconstitution Reconstitute at 500 μg/mL in water.



    Shipping The product is shipped at ambient temperature. Upon receipt, store it immediately at the temperature recommended below.


    Stability & Storage:       Use a manual defrost freezer and avoid repeated freeze-thaw cycles.      

    • 12 months from date of receipt, -20 to -70 °C as supplied.

    • 1 month, 2 to 8 °C under sterile conditions after reconstitution.

    • 3 months, -20 to -70 °C under sterile conditions after reconstitution.


    Background: EBOV GP

    The GP glycoprotein encoded by the genome of Ebola family viruses is a critical molecule for the pathogenicity of   Ebolavirus hemorrhagic viruses (1, 2). It is processed into distinct forms for virus capsule or cell surface presentation or release from virus infected cells. The GP precursor protein is cleaved by furin at a multibasic site to yield a 140 kDa N-terminal fragment (GP1) and a 26 kDa C-terminal fragment (GP2) which remain disulfide linked (3). GP1 is entirely extracellular while GP2 is a transmembrane protein (4). Heterodimers of GP1-GP2 can further associate into trimers (5). GP expressed on virus infected cells can be shed by TACE mediated cleavage, liberating a disulfide linked complex of soluble GP1 and truncated GP2 (4-6). GP binds to multiple C-type lectins on target cell surfaces, including CLEC10A/MGL, DC-SIGN, and DC-SIGNR (7-9). Following internalization, GP1 is cleaved by Cathepsin B and Cathepsin L and then interacts with Niemann-Pick C1 (NPC1) in the endosomal membrane (10-12).

    • References:

      1. Yang, Z.-Y. et al. (2000) Nat. Med. 6:886.

      2. de La Vega, M.-A. et al. (2015) Viral Immunol. 28:3.

      3. Volchkov, V.E. et al. (1998) Proc. Natl. Acad. Sci. USA 95:5762.

      4. Volchkov, V.E. et al. (1998) Virology 245:110.

      5. Sanchez, A. et al. (1998) J. Virol. 72:6442.

      6. Dolnik, O. et al. (2004) EMBO J. 23:2175.

      7. Takada, A. et al. (2004) J. Virol. 78:2943.

      8. Alvarez, C.P. et al. (2002) J. Virol. 76:6841.

      9. Simmons, G. et al. (2003) Virology 305:115.

      10. Schornberg, K. et al. (2006) J. Virol. 80:4174.

      11. Chandran, K. et al. (2005) Science 308:1643.

      12. Cote, M. et al. (2011) Nature 477:344.

    • Long Name:

      Ebola Virus Glycoprotein

    • Entrez Gene IDs:

      911829 (Viral)

    • Alternate Names:

      bovGP; EBOV GP

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