View the results from a comparative study that was performed using a flow cytometer and an image cytometer to examine the T-cell populations from primary human PBMC samples.
Immune cell phenotyping was performed by flow cytometry, and a total of 72 analytes were quantified in heat-inactivated serum samples by multiplex magnetic bead assays or enzyme-linked immunosorbent assay. The hierarchical clustering of cytokines was also pursued.
To develop a more effective approach to identifying different types of blood clots, Zhou and her colleagues took blood samples from a healthy individual and then exposed them to different clotting agents. The team captured thousands of images of the different types of clots using high-throughput imaging flow cytometry.
Spectral flow cytometry was used to look at many different types of immune cells all at the same time, and identify various changes that take place throughout the course of parasitic infection.
Traditionally, flow cytometry is favored for B-cell screening because of its high-throughput, and antibodies secreted from the B-cells can potentially be screened using cold capture. However, this is a representation rather than direct measurement of antibody secretion.
