Mouse Monoclonal GB antibody. Suitable for ICC/IF, Neut, IHC-Fr, ELISA and reacts with Human cytomegalovirus samples. Cited in 6 publications.
Preservative: 0.09% Sodium azide
Constituents: PBS
ICC/IF | Neut | IHC-Fr | ELISA | |
---|---|---|---|---|
Human cytomegalovirus | Expected | Expected | Expected | Expected |
Species | Dilution info | Notes |
---|---|---|
Species Human cytomegalovirus | Dilution info Use at an assay dependent concentration. | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Human cytomegalovirus | Dilution info Use at an assay dependent concentration. | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Human cytomegalovirus | Dilution info Use at an assay dependent concentration. | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Human cytomegalovirus | Dilution info Use at an assay dependent concentration. | Notes - |
Select an associated product type
Envelope glycoprotein that plays a role in host cell entry, cell to-cell virus transmission, and fusion of infected cells. May be involved in the initial attachment via binding to heparan sulfate together with the gM/gN complex that binds heparin with higher affinity. Interacts with host integrin ITGB1, PDGFRA and EGFR that likely serve as postattachment entry receptors. Participates also in the fusion of viral and cellular membranes leading to virus entry into the host cell. Membrane fusion is mediated by the fusion machinery composed at least of gB and the heterodimer gH/gL.
UL55, gB, Envelope glycoprotein B
Mouse Monoclonal GB antibody. Suitable for ICC/IF, Neut, IHC-Fr, ELISA and reacts with Human cytomegalovirus samples. Cited in 6 publications.
Preservative: 0.09% Sodium azide
Constituents: PBS
This antibody is specific for Cytomegalovirus glycoprotein B late neutralizing antigen. Reacts with MRC-5 infected cells but not uninfected cells.
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ab54023, staining Cytomegalovirus Glycoprotein B in monocyte-derived dendritic cells infected with Human cytomegalovirus (VHL/E strain), cultured for 3 hours (left panels) and 24 hours (right panels), by Immunocytochemistry/ Immunofluorescence.
Cells were fixed with paraformaldehyde and permeabilized with 0.2% Triton X-100 in PBS for 10 minutes at room temperature. Samples were incubated with primary antibody and an AlexaFluor®568-conjugated goat anti-mouse monoclonal IgG was used as the secondary antibody.
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