Ki67 expression correlate with a proliferative condition.
So, first of all, because this is a intranuclear staining, you need an unlabeled control (to exclude Ab aspecific interactions and cellular auto-fluorescence).
After that, you have to gate on your cellular population and you must be sure that in every samples (unlabeled, unstimulated and stimulated, for example) there are THE SAME photomultiplier tube (PMT) voltages and compensation matrix.
FInally, you can show your data as SSC/Ki67 or overlay Ki67-histograms of your different conditions.
To know if your data is statistically significant, you can use a stastitic programm, such us Prisma.
Hi Usama, you need to provide more information in detail. Generally speaking, you can first gate T cells, and then measure the propotion of Ki67 under T cells. Higher Ki67 levels represent high proliferation, vice versa.
I have to write a review on Ki67 assay to measure T cell proliferation.
After we apply flow cytometry , we make diagram represents the Ki67 (logarithmic mode) and propidium Iodide (linear mode) , so how can we use this diagram image to understand T cell proliferation ?
Ki67 expression correlate with a proliferative condition.
So, first of all, because this is a intranuclear staining, you need an unlabeled control (to exclude Ab aspecific interactions and cellular auto-fluorescence).
After that, you have to gate on your cellular population and you must be sure that in every samples (unlabeled, unstimulated and stimulated, for example) there are THE SAME photomultiplier tube (PMT) voltages and compensation matrix.
FInally, you can show your data as SSC/Ki67 or overlay Ki67-histograms of your different conditions.
To know if your data is statistically significant, you can use a stastitic programm, such us Prisma.