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Becton Dickinson mouse inflammatory cytokine cytometric bead array kit
Concentrations of TNF‐α, IL‐6 and MCP‐1 in the lung lavage of vaccinated mice. Cytokines and chemokines in the lung lavage of vaccinated and control mice on day 3 after SARS‐CoV infection were assayed by flow cytometry using a mouse inflammatory <t>cytokine</t> (IL‐6, IL‐10, MCP‐1, IFN‐γ, TNF‐α and <t>IL‐12p70)</t> cytometric bead array kit. Bar shows the SEM ( n = 3).
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Concentrations of TNF‐α, IL‐6 and MCP‐1 in the lung lavage of vaccinated mice. Cytokines and chemokines in the lung lavage of vaccinated and control mice on day 3 after SARS‐CoV infection were assayed by flow cytometry using a mouse inflammatory <t>cytokine</t> (IL‐6, IL‐10, MCP‐1, IFN‐γ, TNF‐α and <t>IL‐12p70)</t> cytometric bead array kit. Bar shows the SEM ( n = 3).
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Concentrations of TNF‐α, IL‐6 and MCP‐1 in the lung lavage of vaccinated mice. Cytokines and chemokines in the lung lavage of vaccinated and control mice on day 3 after SARS‐CoV infection were assayed by flow cytometry using a mouse inflammatory <t>cytokine</t> (IL‐6, IL‐10, MCP‐1, IFN‐γ, TNF‐α and <t>IL‐12p70)</t> cytometric bead array kit. Bar shows the SEM ( n = 3).
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Concentrations of TNF‐α, IL‐6 and MCP‐1 in the lung lavage of vaccinated mice. Cytokines and chemokines in the lung lavage of vaccinated and control mice on day 3 after SARS‐CoV infection were assayed by flow cytometry using a mouse inflammatory <t>cytokine</t> (IL‐6, IL‐10, MCP‐1, IFN‐γ, TNF‐α and <t>IL‐12p70)</t> cytometric bead array kit. Bar shows the SEM ( n = 3).
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Concentrations of TNF‐α, IL‐6 and MCP‐1 in the lung lavage of vaccinated mice. Cytokines and chemokines in the lung lavage of vaccinated and control mice on day 3 after SARS‐CoV infection were assayed by flow cytometry using a mouse inflammatory <t>cytokine</t> (IL‐6, IL‐10, MCP‐1, IFN‐γ, TNF‐α and <t>IL‐12p70)</t> cytometric bead array kit. Bar shows the SEM ( n = 3).
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Concentrations of TNF‐α, IL‐6 and MCP‐1 in the lung lavage of vaccinated mice. Cytokines and chemokines in the lung lavage of vaccinated and control mice on day 3 after SARS‐CoV infection were assayed by flow cytometry using a mouse inflammatory <t>cytokine</t> (IL‐6, IL‐10, MCP‐1, IFN‐γ, TNF‐α and <t>IL‐12p70)</t> cytometric bead array kit. Bar shows the SEM ( n = 3).
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Concentrations of TNF‐α, IL‐6 and MCP‐1 in the lung lavage of vaccinated mice. Cytokines and chemokines in the lung lavage of vaccinated and control mice on day 3 after SARS‐CoV infection were assayed by flow cytometry using a mouse inflammatory <t>cytokine</t> (IL‐6, IL‐10, MCP‐1, IFN‐γ, TNF‐α and <t>IL‐12p70)</t> cytometric bead array kit. Bar shows the SEM ( n = 3).
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Concentrations of TNF‐α, IL‐6 and MCP‐1 in the lung lavage of vaccinated mice. Cytokines and chemokines in the lung lavage of vaccinated and control mice on day 3 after SARS‐CoV infection were assayed by flow cytometry using a mouse inflammatory <t>cytokine</t> (IL‐6, IL‐10, MCP‐1, IFN‐γ, TNF‐α and <t>IL‐12p70)</t> cytometric bead array kit. Bar shows the SEM ( n = 3).
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Concentrations of TNF‐α, IL‐6 and MCP‐1 in the lung lavage of vaccinated mice. Cytokines and chemokines in the lung lavage of vaccinated and control mice on day 3 after SARS‐CoV infection were assayed by flow cytometry using a mouse inflammatory <t>cytokine</t> (IL‐6, IL‐10, MCP‐1, IFN‐γ, TNF‐α and <t>IL‐12p70)</t> cytometric bead array kit. Bar shows the SEM ( n = 3).
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Concentrations of TNF‐α, IL‐6 and MCP‐1 in the lung lavage of vaccinated mice. Cytokines and chemokines in the lung lavage of vaccinated and control mice on day 3 after SARS‐CoV infection were assayed by flow cytometry using a mouse inflammatory <t>cytokine</t> (IL‐6, IL‐10, MCP‐1, IFN‐γ, TNF‐α and <t>IL‐12p70)</t> cytometric bead array kit. Bar shows the SEM ( n = 3).
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Concentrations of TNF‐α, IL‐6 and MCP‐1 in the lung lavage of vaccinated mice. Cytokines and chemokines in the lung lavage of vaccinated and control mice on day 3 after SARS‐CoV infection were assayed by flow cytometry using a mouse inflammatory <t>cytokine</t> (IL‐6, IL‐10, MCP‐1, IFN‐γ, TNF‐α and <t>IL‐12p70)</t> cytometric bead array kit. Bar shows the SEM ( n = 3).
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Concentrations of TNF‐α, IL‐6 and MCP‐1 in the lung lavage of vaccinated mice. Cytokines and chemokines in the lung lavage of vaccinated and control mice on day 3 after SARS‐CoV infection were assayed by flow cytometry using a mouse inflammatory <t>cytokine</t> (IL‐6, IL‐10, MCP‐1, IFN‐γ, TNF‐α and <t>IL‐12p70)</t> cytometric bead array kit. Bar shows the SEM ( n = 3).
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Concentrations of TNF‐α, IL‐6 and MCP‐1 in the lung lavage of vaccinated mice. Cytokines and chemokines in the lung lavage of vaccinated and control mice on day 3 after SARS‐CoV infection were assayed by flow cytometry using a mouse inflammatory cytokine (IL‐6, IL‐10, MCP‐1, IFN‐γ, TNF‐α and IL‐12p70) cytometric bead array kit. Bar shows the SEM ( n = 3).

Journal: Microbiology and Immunology

Article Title: Neutralizing antibody against severe acute respiratory syndrome (SARS)‐coronavirus spike is highly effective for the protection of mice in the murine SARS model

doi: 10.1111/j.1348-0421.2008.00097.x

Figure Lengend Snippet: Concentrations of TNF‐α, IL‐6 and MCP‐1 in the lung lavage of vaccinated mice. Cytokines and chemokines in the lung lavage of vaccinated and control mice on day 3 after SARS‐CoV infection were assayed by flow cytometry using a mouse inflammatory cytokine (IL‐6, IL‐10, MCP‐1, IFN‐γ, TNF‐α and IL‐12p70) cytometric bead array kit. Bar shows the SEM ( n = 3).

Article Snippet: Cytokines and chemokines were assayed either using a mouse inflammatory cytokine (IL‐6, IL‐10, MCP‐1, IFN‐γ, TNF‐α and IL‐12p70) cytometric bead array kit (Becton Dickinson, San Jose, CA, USA) ( ) or using the Luminex 200 system (Luminex Co., Austin, TX, USA) as previously reported ( ).

Techniques: Control, Infection, Flow Cytometry