Quantification of Murine AAT by Direct ELISA
dc.contributor.author | Cox, Andrew | |
dc.contributor.author | Mueller, Christian | |
dc.date | 2022-08-11T08:10:13.000 | |
dc.date.accessioned | 2022-08-23T16:59:28Z | |
dc.date.available | 2022-08-23T16:59:28Z | |
dc.date.issued | 2017-07-28 | |
dc.date.submitted | 2017-08-28 | |
dc.identifier.citation | Methods Mol Biol. 2017;1639:217-222. doi: 10.1007/978-1-4939-7163-3_21. <a href="https://doi.org/10.1007/978-1-4939-7163-3_21">Link to article on publisher's site</a> | |
dc.identifier.issn | 1064-3745 (Linking) | |
dc.identifier.doi | 10.1007/978-1-4939-7163-3_21 | |
dc.identifier.pmid | 28752461 | |
dc.identifier.uri | http://hdl.handle.net/20.500.14038/43591 | |
dc.description.abstract | This methods chapter elaborates on how a direct enzyme-linked immunosorbent assay (ELISA) is used to specifically detect and quantify murine alpha-1 antitrypsin (AAT). As a direct ELISA, it lacks some sensitivity as compared to the "sandwich" ELISA method; however, it does reliably differentiate between samples with varying amounts of the mouse AAT protein. This protocol relies on the principle of adsorption to coat each well with sera proteins, whereas detection occurs specifically using a two-step antibody combination. This procedure effectively identifies and quantifies murine AAT from a wide variety of samples including mouse serum, cell culture medium, and cell or tissue lysate. | |
dc.language.iso | en_US | |
dc.relation | <a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=28752461&dopt=Abstract">Link to Article in PubMed</a> | |
dc.relation.url | https://doi.org/10.1007/978-1-4939-7163-3_21 | |
dc.subject | AAT | |
dc.subject | Alpha-1 antitrypsin | |
dc.subject | Direct ELISA | |
dc.subject | Enzyme-linked immunosorbent assay | |
dc.subject | Murine AAT | |
dc.subject | Molecular Biology | |
dc.subject | Research Methods in Life Sciences | |
dc.title | Quantification of Murine AAT by Direct ELISA | |
dc.type | Book Chapter | |
dc.source.booktitle | Methods in molecular biology (Clifton, N.J.) | |
dc.source.volume | 1639 | |
dc.identifier.legacycoverpage | https://escholarship.umassmed.edu/peds_pp/161 | |
dc.identifier.contextkey | 10667372 | |
html.description.abstract | <p>This methods chapter elaborates on how a direct enzyme-linked immunosorbent assay (ELISA) is used to specifically detect and quantify murine alpha-1 antitrypsin (AAT). As a direct ELISA, it lacks some sensitivity as compared to the "sandwich" ELISA method; however, it does reliably differentiate between samples with varying amounts of the mouse AAT protein. This protocol relies on the principle of adsorption to coat each well with sera proteins, whereas detection occurs specifically using a two-step antibody combination. This procedure effectively identifies and quantifies murine AAT from a wide variety of samples including mouse serum, cell culture medium, and cell or tissue lysate.</p> | |
dc.identifier.submissionpath | peds_pp/161 | |
dc.contributor.department | Department of Pediatrics, Division of Pulmonary and Allergy | |
dc.contributor.department | Horae Gene Therapy Center | |
dc.source.pages | 217-222 |