4–7 Currently, isotopic-label antibody panels spanning over 35 proteins are already run regularly via mass cytometry (110 different proteins is the upper limit), and much more information may be obtained from each cell. An illustration of

the revolution in scale this transformative technology provides is that while 10 labels may yield approximately 1,000 possible combinations of cell subsets, 30 yield 1,000,000 (using the Inhibitors,research,lifescience,medical formula X = 2n−1, where X is the number of combinations and n is the number of labels). Of note, useful site repeated runs of a flow cytometer on the same sample, each time measuring a different combination of antibodies, will not have equivalent coverage to the mass cytometer as the data will not be obtained on the same single cell. Thus there is much greater resolving power with the number of labels possible with this new technology, enabling simultaneous quantification of the majority of known immune cell types from an Inhibitors,research,lifescience,medical individual sample, including rare cell subsets (Figure 2). Figure 2 Mass cytometry captures a snapshot of immune system alterations

in cell subset abundance between conditions. Functional Signaling Assays at the Single Inhibitors,research,lifescience,medical Cell Level For primary tissue, original applications of flow cytometry allowed only the quantification of cell surface markers. However, developments over the past decade, primarily in the lab of Garry Nolan at Stanford Inhibitors,research,lifescience,medical University, have enabled the quantification of intracellular proteins, and of particular interest, phosphorylated epitopes.8,9 This allows for accurate quantification at the single cell level of phospho-signaling

biochemistry (phospho-flow). Performed comparatively for a sample between an selleck products unstimulated and stimulated condition, the resultant difference or fold-change is interpreted as the degree of activation of Inhibitors,research,lifescience,medical the specific signaling pathways probed.9,10 With mass cytometry, the strength of this approach has grown even further as it allows multi-parameterization at an even greater scale including Entinostat both cell type and functional response to stimulation by cell surface intracellular markers respectively.4,5,11,12 Thus, the machinery and systems now exist to access the heterogeneity of cellular subsets in the immune system and enable phenotypic characterization and functional assays at a resolution previously unavailable to immunologists. Multiplex Measures of Serum Proteins The immune system is very much dependent on the interactions of various white blood cells with each other, either in synaptic contacts, or at a distance using secreted proteins such as cytokines or chemokines for regulation and response.