Assay for galactose-deficient IgA1 enables mechanistic studies with primary cells from IgA nephropathy patients
Aims: IgA nephropathy, the most common primary glomerulonephritis worldwide, is characterized by glomerular deposition of galactose-deficient IgA1 and elevated serum levels of this IgA1 glycoform. Current ELISA methods lack sensitivity to assess galactose deficiency using small amounts of IgA1, whic...
Wedi'i Gadw mewn:
| Prif Awduron: | , , , |
|---|---|
| Fformat: | Artigo |
| Iaith: | Inglês |
| Cyhoeddwyd: |
Taylor & Francis Group
2018-08-01
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| Cyfres: | BioTechniques |
| Pynciau: | |
| Mynediad Ar-lein: | https://www.future-science.com/doi/10.2144/btn-2018-0042 |
| Tagiau: |
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