
cytometry and microscopy
Intracellular staining and Fc block
When to block Fc receptors, and how to order surface stain, fixation and intracellular antibody so sticky cells do not fake a result.
8 October 2026 · 8 min read
Topic cluster
How flow cytometers and fluorescence microscopes generate a signal, and which controls make that signal interpretable.
26 articles

cytometry and microscopy
When to block Fc receptors, and how to order surface stain, fixation and intracellular antibody so sticky cells do not fake a result.
8 October 2026 · 8 min read

cytometry and microscopy
Why numerical aperture and wavelength set resolution, and how empty magnification enlarges blur without separating detail.
8 October 2026 · 7 min read

cytometry and microscopy
How to match air, water, oil or silicone immersion and the engraved coverslip thickness so a high-NA objective can form a sharp image.
8 October 2026 · 8 min read

cytometry and microscopy
Which biology, antigen density and spillover rules to name before you assign fluorophores or request a cytometer configuration.
8 October 2026 · 7 min read

cytometry and microscopy
How to tell photobleaching from a dim label, and when to change exposure, illumination, binning or gain before the signal is gone.
8 October 2026 · 7 min read

cytometry and microscopy
Which lasers, detectors, filters, formats and sample constraints to answer before you ask for a cytometer or microscope quotation.
8 October 2026 · 7 min read

cytometry and microscopy
Which voltages, thresholds, compensation matrices, lots and gate hierarchies to store so another person can repeat the run.
8 October 2026 · 7 min read

cytometry and microscopy
How to match a sample filter to the nozzle or flow-cell class, and what to do when the event rate collapses from a clog.
8 October 2026 · 8 min read

cytometry and microscopy
How a calibrated scale bar, a linear lookup table and an unsaturated image decide what a research fluorescence figure may claim.
8 October 2026 · 7 min read

cytometry and microscopy
How to build single-stain controls that are bright enough for compensation, and when to branch to cells, beads, or a fresh tube.
8 October 2026 · 8 min read

cytometry and microscopy
What emission overlap, spillover, spreading and a filter window mean when three fluorophores share one cytometer layout.
8 October 2026 · 7 min read

cytometry and microscopy
What no events means on a cytometer: clog, threshold, trigger, sheath, interlock, or a tube that is not actually sipping.
8 October 2026 · 7 min read