Fcap Array: Software Link

The first critical step is the separation of different bead populations. Unlike cellular analysis where scatter plots differentiate lymphocytes from granulocytes, bead arrays rely on consistent fluorescence intensity. FCAP software uses two-dimensional dot plots (e.g., FL-1 vs. FL-2) to draw polygonal or rectangular gates around distinct bead clusters. Advanced algorithms can even compensate for spectral overlap between the bead’s intrinsic dye and the reporter dye, ensuring that a bead’s identity is never misassigned.

After administering a novel vaccine, a core lab uses FCAP software to measure antigen-specific immunoglobulin titers (IgG1, IgG2a, IgA). The software’s ability to handle serial dilutions and report endpoint titers is invaluable. fcap array software

: Supports both qualitative (presence/absence based on controls) and quantitative analysis. Workflow for CBA Data Analysis The first critical step is the separation of

Raw data is useless if it is trapped in a proprietary format. Leading FCAP software exports to: FL-2) to draw polygonal or rectangular gates around