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- W2892347345 abstract "Abstract Immunoglobulin G (IgG) N - glycosylation is crucial for its effector functions. It is a complex trait, and large sample sets are needed to discover multiple genetic factors that underlie it. While in humans such high-throughput studies of IgG N-glycans became usual, only one has been carried out in mice. Here we describe and validate a method for the relative quantification of IgG Fc-linked N - glycans in a subclass-specific manner using nano-reverse phase liquid chromatography coupled with mass-spectrometry (nanoRP-LC-MS) applied to murine IgG. High-throughput data processing is ensured by the LaCyTools software. We have shown that IgG isolation procedure is the main source of technical variation in the current protocol. The major glycoforms were quantified reliably with coefficients of variation below 6% for all the analytes with relative abundances above 5%. We have applied our method to a sample set of 3 inbred strains: BALB/c, C57BL/6 and C3H and observed differences in subclass-specific and strain - specific N - glycosylation of IgG, suggesting a significant genetic component in the regulation of Fc-linked IgG N - glycosylation." @default.
- W2892347345 created "2018-09-27" @default.
- W2892347345 creator A5003751922 @default.
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- W2892347345 date "2018-09-12" @default.
- W2892347345 modified "2023-10-12" @default.
- W2892347345 title "MIgGGly (mouse IgG glycosylation analysis) - a high-throughput method for studying Fc-linked IgG N-glycosylation in mice with nanoUPLC-ESI-MS" @default.
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- W2892347345 doi "https://doi.org/10.1038/s41598-018-31844-1" @default.
- W2892347345 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/6135756" @default.
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- W2892347345 hasPublicationYear "2018" @default.
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