Author:
Wang Xianxia,Wu Liqing,Huang Yanjie,Su Ping,Yang Yi,Yang Bin,Zhang Ning
Publisher
Springer Science and Business Media LLC
Subject
Biochemistry,Analytical Chemistry
Reference41 articles.
1. ISO 17511:2020 In vitro diagnostic medical devices — requirements for establishing metrological traceability of values assigned to calibrators, trueness control materials and human samples.
2. JJF 1752–2019. Calibration specification for automatic enclosed luminescence immunoassay analyzer.
3. Westwood S, Choteau T, Daireaux A, et al. Mass balance method for the SI value assignment of the purity of organic compounds. Anal Chem. 2013;85(6):3118–26.
4. Stoppacher N, Josephs RD, Daireaux A, et al. Accurate quantification of impurities in pure peptide material – angiotensin I: comparison of calibration requirements and method performance characteristics of liquid chromatography coupled to hybrid tandem mass spectrometry and linear ion trap high-resolution mass spectrometry. Rapid Commun Mass Sp. 2015;29(18):1651–60.
5. Melanson JE, Thibeault M-P, Stocks BB, et al. Purity assignment for peptide certified reference materials by combining qNMR and LC-MS/MS amino acid analysis results: application to angiotensin II. Anal Bioanal Chem. 2018;410(26):6719–31.
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