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Even when two laboratories use the same number of ordinal categories, category definitions may differ (compare, for example, Cropley et al. [18] with Dolinoy et al. [19]), thus adding to the difficulty of comparison between studies.
Both laboratories use the same radioimmunoassay kit, which has less than 1% cross-reactivity with C-peptide and proinsulin.
Thirdly, calibration of creatinine assays can also introduce systematic bias, but as both laboratories use the same analytical process, this should be limited.
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Chefs like Ferran Adrià had noticed that a hundred years ago kitchens and science laboratories used the same techniques, but in recent years labs had pulled far ahead.
One lesson learned from inter-genomics studies is that there are core molecular networks that can be identified by multiple laboratories using the same platform.
A reagent grade calcite powder submitted to two independent laboratories using the same method and model instrument gave Kr-BET surface area values that were off by a factor of 3. In this study, we used a total of four different batches of starting material.
The goal of these studies was to determine whether assessment of contractility and hemodynamics, when measured across different laboratories using the same protocol, could consistently detect drug-induced changes in the inotropic state of the heart using drugs known to have clinically relevant positive and negative effects on myocardial contractility.
The same RNA samples were processed independently five times in four different laboratories using the same Affymetrix GeneChip platform.
Following the pioneering electron crystallographic studies of Henderson, Glaeser and colleagues [1], [2] an atomic model for bacteriorhodopsin was first determined from cryo-electron microscopy by Henderson et al and confirmed and extended by work in a number of laboratories using the same method [3] [6].
Experiments were performed in two laboratories using the same procedures.
All laboratories used the same protocol for the whole study period.
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