Signal-onset detection raises dwell time only when needed, helping MRM monitor more compounds with better precision, reliability, and less crosstalk.
Multi-stage ion trapping and fragmentation raise sequence coverage and structural characterization for complex analytes at high scan rates.
Shifted peak alignment in MS/MS data localizes molecular modification sites automatically, reducing manual interpretation time for chemists.
Automatically flags reagent-derived peaks in mass spectra so operators can avoid false positives in metabolite identification.
Correlates AP-ECD or ETD fragment ions with parent ions using elution or drift times, improving mixture analysis and spectral interpretation.
Offset scanning windows and linear reconstruction sharpen precursor m/z assignment in SWATH data without relying on faster mass-filter scans.
Segmented collision cells resolve the speed-sensitivity trade-off in mass spectrometers by routing ions through optimized paths for rapid SRM transitions.
Dynamic dissociation selection optimizes spectral data quality by adapting CAD, ETD, or ECD modes to specific ion charge states.
Collision cell with differential gas conductance directs CID gas flow along ion path to enhance transmission efficiency.
Dynamic collision energy calculation using precursor ion metrics eliminates manual tuning for optimal fragmentation in complex protein mixtures.
Alternating charge reduction and fragmentation modes resolves overlapping species interference by separating parent ions from fragment ions.