Table 2. If you have no prior experience with your cells of interest, it is important to check the literature as a guide.
Ordering Payment methods we support: We wish you all the best with your research. All rights reserved. Depending on their nature, spectral emission overlaps and emission peaks, conjugated antibodies should be wisely chosen for every protocol to avoid the overlapping with fluorochromes with broader excitation curves.
A flow cytometric method to assess antigen-specific proliferative responses of different subpopulations of fresh and cryopreserved human peripheral blood mononuclear cells.. Optimization of 5- and-6 - carboxyfluorescein diacetate succinimidyl ester for labeling human intervertebral disc cells in vitro.. Skip to main content.
Each graph contains an FMO of the stainings red , a blank sample representation blue , single staining green and the same staining in the tube containing all stains yellow.
The journal aims as well to support the medical-biological sciences related to health as to have a space for history, philosophy and ethics. Intracellular staining was performed as follows..
Checking proper compensation of our samples. Following the previously described gating procedures and experimental setups, cells were followed in cell cultures for up to 18 days.
For each sample at least 250 000 cells were collected, and 10 000 signals analyzed.
I'm asking your suggestions and valuable comments in this particular issue. Before beginning, you should also ensure that you include proper controls for accurate data analysis.
Figure 4. An appropriate marker with an important amount of expression must be selected in this channel i.
Figure 5. Determination of lymphocyte division by flow cytometry.. So adding a viability marker such as 7-AAD to identify dead or apoptotic cells is crucial i.