| dc.contributor.author | Nilsson, Per | |
| dc.contributor.author | Pettersen, Kristin | |
| dc.contributor.author | Oppermann, Martin | |
| dc.contributor.author | Skjeflo, Espen Waage | |
| dc.contributor.author | Fure, Hilde | |
| dc.contributor.author | Christiansen, Dorte | |
| dc.contributor.author | Mollnes, Tom Eirik | |
| dc.date.accessioned | 2022-04-26T12:49:21Z | |
| dc.date.available | 2022-04-26T12:49:21Z | |
| dc.date.created | 2022-01-31T13:16:39Z | |
| dc.date.issued | 2021 | |
| dc.identifier.citation | Methods in molecular biology. 2021, 2227 51-59. | en_US |
| dc.identifier.issn | 1064-3745 | |
| dc.identifier.uri | https://hdl.handle.net/11250/2992870 | |
| dc.description.abstract | Enzyme-linked immunosorbent assay (ELISA) enables fast and simple quantification of analytes in the pico- to nanogram range in complex samples. Here, we describe an ELISA for the detection of porcine C3a as a marker for complement activation. Antibody specificity is critical for a robust assay. This assay is based on a pair of antibodies specific for the porcine C3a molecule and thus does not react with native C3. | en_US |
| dc.language.iso | eng | en_US |
| dc.publisher | Springer | en_US |
| dc.title | Quantification of Porcine Complement Activation Fragment C3a by a Neoepitope-Based Enzyme-Linked Immunosorbent Assay | en_US |
| dc.type | Peer reviewed | en_US |
| dc.type | Journal article | en_US |
| dc.description.version | acceptedVersion | en_US |
| dc.rights.holder | This is the authors' accepted manuscript to an article published by Springer. | en_US |
| dc.source.pagenumber | 51-59 | en_US |
| dc.source.volume | 2227 | en_US |
| dc.source.journal | Methods in molecular biology | en_US |
| dc.identifier.doi | 10.1007/978-1-0716-1016-9_5 | |
| dc.identifier.cristin | 1994727 | |
| dc.relation.project | Norges forskningsråd: 223255 | en_US |
| cristin.ispublished | true | |
| cristin.fulltext | postprint | |
| cristin.qualitycode | 1 | |
