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Fig. 1 | Clinical Proteomics

Fig. 1

From: An LC–MS-based designated comparison method with similar performance to the Lp(a) reference measurement procedure to guide molar Lp(a) standardization

Fig. 1

Comparison of imprecision of RMP and DCM based on CLSI EP-15 protocol results. Tests should fulfill predefined analytical performance specifications. For apo(a), the minimum total allowable error (TEa) is concentration dependent (grey line). To divide the error budget over the stakeholders of the metrological traceability chain, ½ of the TEa is allocated for the RMP, and thus ideally also the DCM (red line). EP-15 results are plotted as blue dots (RMP) or green dots (DCM)

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