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Mass cytometers combine time-of-flight mass spectrometry and flow cytometry. Cells are labeled with heavy metal ion-tagged antibodies (usually from the lanthanide series) instead of fluorescently-tagged antibodies and detected using time-of-flight mass spectrometry.
Advantages include minimal overlap in metal signals meaning the instrument is theoretically capable of detecting 100 parameters per cell, entire cell signaling networks can be inferred organically without reliance on prior knowledge, and one well-constructed experiment produces large amounts of data.