For immunochemical detection of AcMNPV major envelope glycoprotein
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AcMNPV Major Envelope Glycoprotein Neutralizing Antibody (Clone M001)

Item No. 37014

Technical Information
Synonyms
  • AcMNPV GP64
  • Autographa californica Multicapsid Nucleopolyhedrovirus Major Envelope Glycoprotein
  • Autographa californica Multiple Nucleopolyhedrovirus Major Envelope Glycoprotein
Immunogen
Recombinant AcMNPV (strain E2)
Clone Designation
M001
200 or 500 µg of protein A-affinity purified monoclonal antibody
Storage Buffer
0.2 μm filtered solution in PBS
Host
Mouse
Isotype
IgG1
Applications
MN
Cross Reactivity
(+) Major envelope glycoprotein
Species Reactivity
(+) AcMNPV
Shipping & Storage Information
Storage
-80°C
Shipping
Dry ice in continental US; may vary elsewhere
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    Product Description

    Autographa californica multiple nucleopolyhedrovirus (AcMNPV) major envelope glycoprotein is a class III viral fusion protein.1 AcMNPV is a double-stranded DNA insect virus and member of the Baculoviridae family. AcMNPV major envelope glycoprotein exists as a trimer and is composed of five domains in the low pH, post-fusion state that is highly post-translationally modified via glycosylation sites and a palmitoylation site at the C-terminus.2,3 It is expressed on the surface of infected cells and budded virions.1 AcMNPV major envelope glycoprotein is involved in viral envelope-host cell endosome membrane fusion in a low pH-dependent manner and in virion budding.4,5 Lipoplexes containing AcMNPV major envelope glycoprotein have been used for gene delivery to mammalian cells, which can be inhibited by an AcMNPV major envelope glycoprotein neutralizing antibody.6 Cayman’s AcMNPV Major Envelope Glycoprotein Neutralizing Antibody (Clone M001) can be used for microneutralization (MN) assays.

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Yu, Q., Bai, L., Ji, N., et alCritical residues and contacts within domain IV of Autographa californica multiple nucleopolyhedrovirus GP64 contribute to its refolding during membrane fusion. J. Virol. 94(19), e01105-01120 (2020).

    2. Kadlec, J., Loureiro, S., Abrescia, N.G.A., et alThe postfusion structure of baculovirus GP64 supports a unified view of viral fusion machines. Nat. Struct. Mol. Biol. 15(10), 1024-1030 (2008).

    3. Zhang, S.X., Han, Y., and Blissard, G.W. Palmitoylation of the Autographa californica multicapsid nucleopolyhedrovirus envelope glycoprotein GP64: Mapping, functional studies, and lipid rafts. J. Virol. 77(11), 6265-6273 (2003).

    4. Hu, L., Li, Y., Ning, Y.-J., et alThe major hurdle for effective baculovirus transduction into mammalian cells is passing early endosomes. J. Virol. 93(15), e00709-00719 (2019).

    5. Oomens, A.G.P., and Blissard, G.W. Requirement for GP64 to drive efficient budding of Autographa californica multicapsid nucleopolyhedrovirus. Virology 254(2), 297-314 (1999).

    6. Guibinga, G.-H., Song, S., Loring, J., et alCharacterization of the gene delivery properties of baculoviral-based virosomal vectors. J. Virol. Methods. 148(1-2), 277-282 (2008).