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MS spectra were processed in flexAnalysis.
The acquired spectra were processed in FlexAnalysis (Bruker).
Mass spectra were processed in FlexAnalysis (Bruker Daltonics) with baseline subtraction and peak detection of the IgG1 and IgG2 glycopeptide signals.
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Spectra were processed in VnmrJ®.
Samples were generated and processed in triplicate.
The mass spectra were visualized and processed using FlexAnalysis software.
Data were processed with FlexAnalysis 3.0 (Bruker Daltonics).
Data were processed using FlexAnalysis v3.4 and FlexImaging v3.0 (Bruker Daltonics); ion filters were set to m/ z ± 0.25 and images normalized to total ion count.
Next, IgG galactosylation was analysed by performing matrix-assisted laser desorption/ionization time of flight mass spectrometry to detect tryptic glycopeptides, and mass spectra of IgG1 and IgG2 were processed using FlexAnalysis software (Bruker Daltonics, Wormer, The Netherlands).
The sample spectra acquired were processed using flexAnalysis v3.3 (Bruker Daltonics GmbH) by performing baseline subtraction, smoothening and internal calibration based on the theoretical monoisotopic masses of APLP1 fragments 1β17 (1615.79 m/z), 1β18 (1728.88 m/z), 1β22 (2143.11 m/z), 1β25 (2328.19 m/z), 1β27 (2472.24 m/z) and 1β28 (2585.32 m/z).
The spectra were processed using the flexAnalysis software (Bruker Daltonics).
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