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Beckman immage immunochemistry system

Manufactured by Beckman Coulter
Sourced in United States

The Beckman Immage Immunochemistry system is a diagnostic instrument designed for the quantitative determination of various analytes in human biological samples. The system utilizes an immunochemical approach to provide accurate and reliable results for clinical laboratories.

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7 protocols using beckman immage immunochemistry system

1

Evaluation of Biochemical Biomarkers

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Biochemical parameters were measured using routine laboratory methods. Serum high-sensitivity C-reactive protein (hs-CRP) level was determined with a high-sensitivity nephelometric method using the Beckman IMMAGE Immunochemistry System (Beckman Instruments, Fullerton, CA), which has a minimum level of detection of 0.2 mg/L. Serum levels of TNF-α were assayed with enzyme-linked immunosorbent assay (ELISA) kits (R&D Systems Inc., Minneapolis, MN, USA) according to the manufacturer's instructions. The minimum levels of detection were 1.6 pg/mL for TNF-α. The intra- and interassay coefficients of variation for measurements of hs-CRP and TNF-α were 2.7% and 5.0%, respectively, and 3.0% and 6.9%, respectively.
High-sensitive troponin T was measured using Cobas Troponin T hs (highly sensitive) STAT (short turn-around time) (Roche Diagnostics). The assay working range is reported as 3–10 000 ng/L, with an interassay CV, according to the manufacturer, of 3.1% at 24 ng/L and 1.3% at 300 ng/L. The lower limit of quantification is 13 ng/L, the limit of detection is 5 ng/L, and the limit of blank is 3 ng/L, as listed by the manufacturer.
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2

Albumin-based Blood-CSF Barrier Evaluation

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Serum and CSF albumin concentrations were measured by immunonephelometry on a Beckman Immage Immunochemistry system (Beckman Instruments, Beckman Coulter, Brea, CA, USA). QAlb was calculated as the ratio of CSF albumin (mg/L) to serum albumin (g/L)33 (link).
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3

Albumin Ratio Measurement Protocol

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Participants underwent morning fasting venous blood draw and samples were immediately stored at −80°C. Whole blood was centrifuged at 2000g and 4°C for 15 min and plasma was extracted and stored in ten 0.5mL aliquots. Albumin levels (plasma and CSF) were measured by immunonephelometry on a Beckman Immage Immunochemistry system (Beckman Instruments, Beckman Coulter, Brea, CA, USA). The albumin ratio was calculated as CSF albumin (mg/L) / plasma albumin (g/L).
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4

Blood-Brain Barrier Permeability Assessment

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Serum and CSF concentrations of albumin were measured by immunonephelometry on a Beckman IMMAGE Immunochemistry system (Beckman Instruments, Beckman Coulter, Brea, CA, USA) at the Clinical Neurochemistry Laboratory in Mölndal, Sweden, using a method accredited by the Swedish Board for Accreditation and Conformity Assessment (SWEDAC). Intra- and inter-assay coefficients of variation were below 10%. The ratio between the albumin concentration in CSF (mg/L) and serum (g/L) was calculated and used to assess blood–brain barrier function [21 (link)].
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5

Albumin Levels in CSF and Serum

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Albumin levels in CSF and serum were measured at the Clinical Neurochemistry Laboratory in Mölndal, Sweden, by immunonephelometry on a Beckman Immage Immunochemistry system (Beckman Instruments, BeckmanCoulter, Brea, CA, USA). The method was accredited by the Swedish Board for Accreditation and Conformity Assessment (SWEDAC). Experienced and board-certified laboratory technicians who were blinded to clinical information performed all measurements. Intra- and inter-assay coefficients of variation were below 10%. To assess the blood CSF barrier function, the ratio between albumin concentration in CSF (mg/L) and serum (g/L) was calculated.
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6

Biomarker Measurement in Neurodegeneration

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Albumin levels in serum and CSF were measured by immunonephelometry on a Beckman Immage Immunochemistry system (Beckman Instruments, Beckman Coulter, Brea, CA, USA). The albumin ratio was calculated as CSF albumin (mg/L)/serum albumin (g/L) and was used as a measure of the blood-brain barrier function. T-tau was measured using a sandwich ELISA (INNOTEST hTAU-Ag, Fujirebio, Ghent, Belgium) specifically constructed to measure all tau isoforms irrespective of phosphorylation status. Tau phosphorylated at threonine 181 (P-tau) was measured using a sandwich ELISA (INNOTEST Phospho-Tau[181P], Fujirebio). Aβ-related biomarkers (A38, A40, A42, secreted amyloid precursor protein  [sAPP] and secreted amyloid precursor protein  [sAPP]) were analyzed using Meso Scale assays (Meso Scale Discovery, Rockville, MD, USA) according to kit inserts. All samples were analyzed on the same plates using the same batch of reagents by board-certified laboratory technicians who were blinded to clinical information. Intra-assay coefficients of variation were below 10% for all analytes.
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7

Albumin Concentration Analysis in Serum and CSF

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Serum and CSF concentrations of albumin were analyzed by immunonephelometry on a Beckman Immage Immunochemistry system (Beckman Instruments, Beckman Coulter, Brea, CA, USA), using a method accredited by the Swedish Board for Accreditation and Conformity Assessment (SWEDAC). Intra-and inter-assay coefficients of variation were below 10%. The ratio between the albumin concentration in CSF (mg/L) and serum (g/L) was calculated and used to assess blood-CSF barrier function (Andersson et al. 1994 ).
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