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Hydrasys platform

Manufactured by Sebia
Sourced in France

The Hydrasys platform is a fully automated system for the electrophoresis and densitometry analysis of biological samples. It is designed to perform various electrophoresis techniques, including serum protein, urine, and hemoglobin analysis. The Hydrasys platform automates the entire process, from sample preparation to data analysis, providing consistent and reliable results.

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Lab products found in correlation

2 protocols using hydrasys platform

1

Comprehensive Immunological Analysis of CSF and Blood

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Blood and CSF were collected for all patients and analyzed in the Nice University Hospital immunology laboratory. Blood and CSF IgG, albumin, and KFLC were measured by turbidimetry with the analyzer Optilite (The Binding Site, Birmingham, UK) using the serum-free light chain immunoassay Freelite (The Binding Site, Birmingham, UK), according to the manufacturer's instructions. Oligoclonal bands were determined by isoelectric focusing on agarose gel using subsequent immunoblotting using IgG-specific antibody staining (Hydrasys platform; Sebia, Lisses, France). Oligoclonal band patterns were evaluated by an experienced biologist and classified as positive (patterns II and III) or negative (other patterns). A cutoff of ≥ 2 CSF-restricted bands was used to define OCB positivity. The determination of intrathecal synthesis of KFLC was evaluated by the calculation of the K-index using the formula:
K-index = (CSF KFLC/serum KFLC)/(CSF albumin/serum albumin). According to previously published data, a K-index of ≥8.9 was considered as positive.17 (link)
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2

Immunological Biomarkers in Neurological Diagnosis

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Blood and cerebrospinal fluid (CSF) were collected and analyzed in the Nice University Hospital immunology laboratory. Blood and CSF IgG, albumin, and KFLC were measured by turbidimetry with the analyzer Optilite (The Binding Site, Birmingham, UK) using the serum‐free light chain immunoassay Freelight (The Binding Site, Birmingham, UK), according to the manufacturer's instructions. Oligoclonal bands (OCB) were determined by isoelectric focusing on agarose gel using subsequent immunoblotting using IgG‐specific antibody staining (Hydrasys platform; Sebia, Lisses, France). OCB patterns were evaluated by an experienced biologist and classified as positive (patterns II and III) or negative (other patterns). The determination of intrathecal synthesis of KFLC was evaluated by calculating the K‐index using the formula: K‐index = (CSF KFLC/serum KFLC)/(CSF albumin/serum albumin).
32 (link),
33 (link) A cutoff ≥2 CSF restricted bands or K‐index ≥8.92 defined CSF positivity.
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