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Hydrasys 2 system

Manufactured by Sebia
Sourced in Netherlands, France

The Hydrasys 2 system is a high-performance electrophoresis instrument designed for the separation and analysis of proteins in biological samples. It is capable of performing a variety of electrophoresis techniques, including agarose gel electrophoresis and immunofixation electrophoresis.

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3 protocols using hydrasys 2 system

1

Hydrashift Assay for Daratumumab Detection

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Patient samples were run on both the Hydrashift assay and a standard IF gel for comparison. Both assays were performed on the Hydrasys 2 system (Sebia) using the Hydragel 4 IF kit (Sebia). The Hydrashift procedure is similar to that of a normal IF, except that the antidaratumumab antiserum is applied to the gel with an additional applicator. A positive control sample was run daily. Both assays were performed according to the manufacturer’s instructions.
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2

Exercise-induced vWF and Platelet Function

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Blood samples were collected at baseline, 4 min after the start of exercise, during peak exercise and at 5, 10 and 30 min after exercise (figure 1) using peripheral venous access with a 3 mm needle in the arm or hand. From these blood samples, the HMW-multimer ratio of vWF (HMWMs) and CT-ADP were measured. HMWMs was defined as the relative amount of HMW-multimers (larger than 15-mers) in the sample compared with normal pooled plasma (NPP; standard human plasma) as previously described.29 (link) This ratio of HMW-multimers to normal pooled plasma equals 1 without any abnormalities and becomes <1 when the HMW-multimer ratio is reduced. The CT-ADP was measured using the Platelet Function Analyzer (PFA)−100 (Siemens Medical Solutions Diagnostics, Netherlands), vWF multimers were analysed on a Hydrasys 2 system using ‘Hydragel von Willebrand Multimers’ and ‘von Willebrand Multimers Visualisation’ kits (all from SEBIA, Belgium). Analysis of CT-ADP with the point-of-care assay PFA-100 is used as a surrogate marker of vWF loss. Higher values correspond to a longer closure time and more loss of vWF. All assessments were done in our tertiary hospital laboratory with laboratory personnel blinded to clinical data.
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3

Serum Protein Analysis Protocol

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The serum samples used for this study were submitted to the laboratory for serum protein analysis in the Region Västra Götaland, Sweden, during 2015–2020. The data was accessed for research on July 5th, 2021. All samples were analyzed on both an automated capillary electrophoresis system (Capillarys 2 Flex Piercing, SEBIA, Issy-les-Moulineaux, France), for quantification, as well as by a semi-automated agarose gel technology system (serum gel electrophoresis) (Hydrasys 2 System and PENTA PN 1260 kit, SEBIA, Issy-les-Moulineaux, France) [8 (link),9 (link)] to not miss small fractions of M-protein. For samples where a suspected M-protein was present (based on the results from the capillary SPEP and gel SPEP), immunofixation (Hydrasys 2 System and Hydrasys IF kit, SEBIA, Issy-les-Moulineaux, France) was performed to determine the type of M-protein. M-proteins were quantified based on the capillary zone electrophoresis (CZE) (S1 Fig) using the SEBIA software (Phoresis, SEBIA, Issy-les-Moulineaux, France).
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