diff --git a/tables/flow_mabs.tex b/tables/flow_mabs.tex
new file mode 100644
index 0000000..edaf0bd
--- /dev/null
+++ b/tables/flow_mabs.tex
@@ -0,0 +1,12 @@
+\begin{tabular}{@{\extracolsep{5pt}} ccccc}
+  \\[-1.8ex]\hline 
+  \hline \\[-1.8ex] 
+  Antigen & Fluorophore & Vendor & Catalog Number & Purpose \\
+  \hline \\[-1.8ex]
+  CD3 & APC-Fire & \bl{} & 34839 & Differentiation, Degranulation \\
+  CD4 & PerCP-Cy5.5 & \bl{} & 344607 & Differentiation, Degranulation \\
+  CCR7 & AF647 & \bd{} & 560816 & Differentiation \\
+  CD62L & PE & \bd{} & 341012 & Differentiation \\
+  CD107a & AF647 & \bd{} & 562622 & Degranulation \\
+  \hline \\[-1.8ex]
+\end{tabular} 
\ No newline at end of file
diff --git a/tex/thesis.tex b/tex/thesis.tex
index 6b834bd..209e4c2 100644
--- a/tex/thesis.tex
+++ b/tex/thesis.tex
@@ -195,6 +195,7 @@
 \newcommand{\thermo}{Thermo Fisher}
 \newcommand{\miltenyi}{Miltenyi Biotech}
 \newcommand{\bl}{Biolegend}
+\newcommand{\bd}{Becton Dickenson}
 
 % the obligatory misc category
 \newcommand{\inlinecode}{\texttt}
@@ -1143,7 +1144,12 @@ context of pure error). Statistical significance was evaluated at $\upalpha$ =
 \end{figure*}
 
 % METHOD add flow cytometry
-% TABLE add a list of all antibodies used
+
+\begin{table}[!h] \centering
+  \caption{\glspl{mab} used for flow cytometry}
+  \label{tab:flow_mabs}
+  \input{../tables/flow_mabs.tex}
+\end{table}
 
 \section{results}
 
@@ -1448,7 +1454,6 @@ cells after \SI{14}{\day} were on the interior surface of the \glspl{dms}
 
 % TODO double check the timing of this experiment (it might not be day 14)
 
-% TABLE provide the regression results and coefficients from this
 \begin{figure*}[ht!]
   \begingroup