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cise quanti fi cation of Cu , Zn-SOD in human red blood cells using species-speci fi c double and triple IDMS †
| Content Provider | Semantic Scholar |
|---|---|
| Author | Gleitzmann, Julia Raab, Andrea Schulze, Dirk Wätzig, Hermann Feldmannb, Jörg Swarta, Claudia |
| Copyright Year | 2016 |
| Abstract | Cu,Zn-superoxide dismutase (SOD1) is a protein involved in the antioxidant defense system of the body responsible for the dismutation of the superoxide anion. It contains two Cu and two Zn ions per molecule. As this protein is also involved in several diseases it is used in clinical diagnostics as a biomarker, which requires the accurate and reliable determination of SOD1. Therefore, a candidate reference measurement procedure for the quantification of this protein in human erythrocytes was developed using species-specific isotope dilution mass spectrometry (IDMS), a method giving results traceable to the International System of Units (SI). The measurement procedure was validated with regard to a metrological point of view. Commercially available SOD1 was thoroughly characterized to be used as a pure protein calibration standard in IDMS approaches. Furthermore, Cu and Zn labeled SOD1 was produced to be used as a spike material required for species-specific IDMS. Finally, SOD1 was quantified in human erythrocytes using both double and triple IDMS and a complete uncertainty budget for both approaches was estimated according to the Guide to the Expression of Uncertainty in Measurement (GUM). A calculated mass fraction of SOD1 with its associated expanded uncertainty of (63.94 0.93) mg g 1 (n 1⁄4 30) for double and (64.02 0.96) mg g 1 (n 1⁄4 30) for triple IDMS was obtained. |
| File Format | PDF HTM / HTML |
| Alternate Webpage(s) | https://pubs.rsc.org/en/content/articlepdf/2016/ja/c5ja00459d |
| Language | English |
| Access Restriction | Open |
| Content Type | Text |
| Resource Type | Article |
