ADD flow mabs
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\begin{tabular}{@{\extracolsep{5pt}} ccccc}
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\\[-1.8ex]\hline
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\hline \\[-1.8ex]
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Antigen & Fluorophore & Vendor & Catalog Number & Purpose \\
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\hline \\[-1.8ex]
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CD3 & APC-Fire & \bl{} & 34839 & Differentiation, Degranulation \\
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CD4 & PerCP-Cy5.5 & \bl{} & 344607 & Differentiation, Degranulation \\
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CCR7 & AF647 & \bd{} & 560816 & Differentiation \\
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CD62L & PE & \bd{} & 341012 & Differentiation \\
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CD107a & AF647 & \bd{} & 562622 & Degranulation \\
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\hline \\[-1.8ex]
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\end{tabular}
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@ -195,6 +195,7 @@
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\newcommand{\thermo}{Thermo Fisher}
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\newcommand{\miltenyi}{Miltenyi Biotech}
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\newcommand{\bl}{Biolegend}
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\newcommand{\bd}{Becton Dickenson}
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% the obligatory misc category
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\newcommand{\inlinecode}{\texttt}
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@ -1143,7 +1144,12 @@ context of pure error). Statistical significance was evaluated at $\upalpha$ =
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\end{figure*}
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% METHOD add flow cytometry
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% TABLE add a list of all antibodies used
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\begin{table}[!h] \centering
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\caption{\glspl{mab} used for flow cytometry}
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\label{tab:flow_mabs}
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\input{../tables/flow_mabs.tex}
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\end{table}
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\section{results}
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@ -1448,7 +1454,6 @@ cells after \SI{14}{\day} were on the interior surface of the \glspl{dms}
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% TODO double check the timing of this experiment (it might not be day 14)
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% TABLE provide the regression results and coefficients from this
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\begin{figure*}[ht!]
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\begingroup
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