Viral EBOV GP Antibody Summary
Ile33-Arg501
Accession # Q05320
Applications
Please Note: Optimal dilutions should be determined by each laboratory for each application. General Protocols are available in the Technical Information section on our website.
Scientific Data
Detection of EBOV GP by Western Blot. Western blot shows Recombinant EBOV GP. PVDF membrane was probed with 2 µg/mL of Mouse Anti-Viral EBOV GP Monoclonal Antibody (Catalog # MAB9016) followed by HRP-conjugated Anti-Mouse IgG Secondary Antibody (Catalog # HAF018). A specific band was detected for EBOV GP at approximately 150 kDa (as indicated). This experiment was conducted under reducing conditions and using Immunoblot Buffer Group 1.
Reconstitution Calculator
Preparation and Storage
- 12 months from date of receipt, -20 to -70 °C as supplied.
- 1 month, 2 to 8 °C under sterile conditions after reconstitution.
- 6 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).
- Yang, Z.-Y. et al. (2000) Nat. Med. 6:886.
- de La Vega, M.-A. et al. (2015) Viral Immunol. 28:3.
- Volchkov, V.E. et al. (1998) Proc. Natl. Acad. Sci. USA 95:5762.
- Volchkov, V.E. et al. (1998) Virology 245:110.
- Sanchez, A. et al. (1998) J. Virol. 72:6442.
- Dolnik, O. et al. (2004) EMBO J. 23:2175.
- Takada, A. et al. (2004) J. Virol. 78:2943.
- Alvarez, C.P. et al. (2002) J. Virol. 76:6841.
- Simmons, G. et al. (2003) Virology 305:115.
- Schornberg, K. et al. (2006) J. Virol. 80:4174.
- Chandran, K. et al. (2005) Science 308:1643.
- Cote, M. et al. (2011) Nature 477:344.
Product Datasheets
Citations for Viral EBOV GP Antibody
R&D Systems personnel manually curate a database that contains references using R&D Systems products. The data collected includes not only links to publications in PubMed, but also provides information about sample types, species, and experimental conditions.
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Interferon-Induced HERC5 Inhibits Ebola Virus Particle Production and Is Antagonized by Ebola Glycoprotein
Authors: E Paparisto, NR Hunt, DS Labach, MD Coleman, EJ Di Gravio, MJ Dodge, NJ Friesen, M Côté, A Müller, T Hoenen, SD Barr
Cells, 2021-09-13;10(9):.
Species: Human
Sample Types: Cell Lysates
Applications: Western Blot -
IgY antibodies against Ebola virus possess post-exposure protection in a murine pseudovirus challenge model and excellent thermostability
Authors: Y Zhang, Y Wei, Y Li, X Wang, Y Liu, D Tian, X Jia, R Gong, W Liu, L Yang
PloS Neglected Tropical Diseases, 2021-03-12;15(3):e0008403.
Species: Hamster, Human, Primate
Sample Types: Cell Lysates
Applications: Western Blot
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