We're working hard to help you work smarter. Mass cytometry is an end-to-end solution combining reagents, off-the-shelf preconjugated antibodies, data analysis and instrumentation for high-parameter single-cell protein research. Streamlined experimental design is even simpler with our new interactive web-based panel design tool. We’re continually growing our catalog of preconjugated antibodies to help your lab generate data faster in the quest to uncover hidden drivers of biological systems.
Mass cytometry's expanding breadth and depth empower researchers to answer questions that hadn’t even been imagined previously. CyTOF users are publishing results of novel discoveries at the functional protein level; you can find that research on this page. We're doing our best to help you work smarter so you'll choose Fluidigm as your lab partner.
Maxpar panel designer
An interactive web application to simplify and optimize panel design, the Maxpar® panel designer uses metal-conjugated antibodies from the Fluidigm catalog and custom conjugates. The tool calculates predicted signal overlap for each panel and provides a visualization and algorithm for optimizing each target's metal tag selections for peak performance. Save, export and share panels with collaborators and import reports with CyTOF instrument software.
To access Maxpar antibodies, select "Design" in the Fluidigm custom assay application.
New Maxpar metal-conjugated antibodies
To accelerate your research, we’re constantly adding off-the-shelf metal-conjugated antibodies to our existing catalog. There are already 13 predefined panel kits and more than 300 antibodies available. Review the newest selections, or review the full Maxpar catalog.
Mass cytometry inroads
Researchers around the world are discovering potentially world-changing advances using CyTOF. See our collection of relevant research citations below, or download the Mass Cytometry Publications list.
Becher, B. et al. "High-dimensional analysis of the murine myeloid cell system." Nature Immunology 15(12) (2014): 1,181–9.
Behbehani, G.K. et al. "Transient partial permeabilization with saponin enables cellular barcoding prior to surface marker staining." Cytometry Part A 85(12) (2014): 1,011–9.
Edgar, L.J. et al. "Identification of hypoxic cells using an organotellurium tag compatible with mass cytometry." Angewandte Chemie 53(43) (2014): 11,473–7.
Fergusson, J.R. et al. "CD161 defines a transcriptional and functional phenotype across distinct human T cell lineages." Cell Reports 9(3) (2014): 1,075–88.
Gaudilliere, B. et al. "Clinical recovery from surgery correlates with single-cell immune signatures." Science Translational Medicine 6(255) (2014): 255ra131.
Krishnaswamy, S. et al. "Systems biology. Conditional density-based analysis of T cell signaling in single-cell data." Science 346(6213) (2014): 1250689.
Mingueneau, M. et al. "Single-cell mass cytometry of TCR signaling: amplification of small initial differences results in low ERK activation in NOD mice." Proceedings of the National Academy of Sciences of the United States of America. 111 (46) (2014): 16,466–71.
O'Gorman, W.E. et al. "The split virus influenza vaccine rapidly activates immune cells through Fc(gamma) receptors." Vaccine 32(45) (2014): 5,989–97.
Sachs, Z. et al. "NRASG12V oncogene facilitates self-renewal in a murine model of acute myelogenous leukemia." Blood 124(22) (2014): 3,274–83.
Strauss-Albee, D.M. et al. "Coordinated regulation of NK receptor expression in the maturing human immune system." The Journal of Immunology 193(10) (2014): 4,871–9.
Swadling, L. et al. "A human vaccine strategy based on chimpanzee adenoviral and MVA vectors that primes, boosts, and sustains functional HCV-specific T cell memory." Science Translational Medicine 6(261) (2014): 261ra153.
Yao, Y. et al. "CyTOF supports efficient detection of immune cell subsets from small samples. Journal of Immunological Methods 415 (2014): 1–5.