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Vista 1500

Manufactured by Siemens
Sourced in United States, France

The Vista 1500 is a versatile lab equipment product manufactured by Siemens. It is designed to perform a wide range of analytical tasks in a laboratory setting. The core function of the Vista 1500 is to provide precise and reliable measurements and data analysis for scientific research and testing purposes.

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11 protocols using vista 1500

1

CSF Biomarker Analysis Methods

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Technical specifications for the analytical equipment used in CSF analysis have been outlined in the methods section of the 2017 manuscript by McCudden et al3 (link):
CSF-TP was analysed on three different instruments over the course of the 20 years included in the study as follows: Roche Hitachi 917, 1 January 1996 to 30 September 2001; Beckman Lx20, 30 September 2001 to 1 April 2009 and Siemens Vista 1500, 1 April 2009 to 1 December 2016. The Roche method is based on a benzethonium chloride turbidimetric analysis, whereas the Beckman and Siemens methods use a pyrogallol red-molybdate complex, which is measured at 600 nm. In all cases, analyses were performed according to the manufacturer’s directions.
Other laboratory values were measured on different instruments across the two decades included in the study. Serum creatinine, TP and CSF glucose were measured on the platforms described above for the same time frames; creatinine was measured by the Jaffe method from 30 September 2001 to 13 April 2013 and by the enzymatic method thereafter. CSF WCC and RCC counts were determined using the Beckman Coulter between 1996 and 2009 and the Sysmex XE5000 from 2009 to 2016. All laboratory analyses were determined according to the manufacturer’s instructions throughout the study in a routine clinical laboratory in an academic medical centre (The Ottawa Hospital).
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2

Establishing Chloride Concentration Range

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The laboratory tools used in our institution are as follows: 1) arterial blood gas analyzer (RAPIDLab 1265; Siemens Healthcare Diagnostics Inc., Tarrytown, NY, USA); 2) CBC (ADVIA2120i, Siemens Healthcare Diagnostics Inc.); and 3) chemical electrolyte analyzer (VISTA 1500; Siemens Healthcare Diagnostics Inc.). According to our machine, the normal range of the concentration of serum chloride is 98 to 107 mmol/L. Above 107 mmol/L will be defined as hyperchloremia.
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3

Metabolic Biomarkers in Experimental Analyses

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Serum total cholesterol (TC), high density lipoprotein cholesterol (HDL-C) and low density lipoprotein cholesterol (LDL-C), triglycerides (TGs), glucose (Glu), aspartate aminotransferase (AST), and alanine aminotransferase (ALT) levels were measured by the enzymatic procedures run on Siemens Vista 1500 instrumentation (Clinical laboratory of Richmond VA Medical Center). Serum insulin was measured by the sensitive ELISA sandwich assay method using Crystal Chem Ultra-sensitive mouse insulin ELISA kit (Elk Grove Village, IL, catalogue # 90080) according to manufacturer’s instruction. IR was assessed by using homeostasis model assessment of insulin resistance (HOMA-IR) score calculated as [glucose (mg/dl) x insulin (ng/ml) × 26 / 405]. Liver TC was measured by the enzymatic assay using the Cholesterol E Kit (FUJIFILM Wako Chemicals, catalogue # 999-02601). Infinity Triglycerides Kit (Thermo Fisher Scientific, catalogue # 22421) was used for liver TG measurement. Abcam free fatty acid (FFA) assay kit (catalogue # Ab65341) was used for the liver FFA measurements.
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4

Quantification of Iron Homeostasis Markers

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Serum iron, ferritin, transferrin, C-reactive protein (CRP) and soluble transferrin receptor (sTfR) were quantified using the Dimension RXL and Vista 1500 system (Siemens Healthcare, Saint-Denis, France). Transferrin saturation (TS) was calculated as the percent of [serum iron (μmol/L) / serum transferrin (g/L) × 25]. The hemoglobin level was measured on an automated counter (Sysmex, Roissy, France), and quantification of IL-6 was performed using a cytometric bead array (BD Bioscience, Le Pont de Cliax, France). Serum hepcidin was quantified by the previously published method of LC-MSMS.30 (link) Biological markers for each subgroup were expressed in mean±Standard Error of Mean (SEM).
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5

Vitamin D and Calcium Analysis Protocol

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Blood samples were collected and centrifuged at 3500 rpm for 15 minutes prior to freezing at −20°C. Serum was thawed prior to analysis for quantification of 25-hydroxyvitamin D (25(OH)D) via a manual radioimmunoassay (Immunodiagnostics Systems Limited, UK) using 125iodine-labelled 25-hydroxyvitamin D. The method measures total (D2 plus D3) 25-hydroxyvitamin D. Serum calcium was quantified with the RXL Dimension or Vista 1500 platforms (Siemens Healthcare Diagnostics, USA). Analysis was performed in a tertiary referral laboratory, fully accredited to the standard required by the National Australian Testing Authority (NATA) (Pathology North, Hunter New England). Vitamin D status in analysis was categorised as deficiency (50 nmol/L (≤20 ng/mL)), insufficiency (52.5–72.5 nmol/L (>20.0 ≤29 ng/mL)), and normal (72.5 nmol/L (>30 ng/mL)) [3 (link)].
All samples were collected within spring season of 2006 (September–November), average daily temperature 24.4°C (range 21.5–28.5°C), and average daily global solar exposure 20.0 MJ/m2 (range 17.2–23.2 MJ/m2) [24 ]. Longitude and latitude of study area ranged between 151.16E and 152.01E and 32.68S and 33.5S.
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6

Comprehensive Metabolic Biomarker Measurement

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Serum creatinine was determined with an enzymatic assay on a cobas 8000 c 702 (Roche Diagnostics) or a Vista 1500 (Siemens Healthineers). HbA1c was assessed with the TOSOH G8 and G11 HPLC Analyzer (Sysmex). Plasma adrenaline and noradrenaline were measured with high-performance liquid chromatography in combination with fluorometric detection. Plasma glucagon was measured with radioimmunoassay analysis (Euro Diagnostica). Plasma insulin was analyzed with an in-house radioimmunoassay. Plasma cortisol and growth hormone were measured via a routine analysis method with an electrochemiluminescent immunoassay on a MODULAR ANALYTICS E170 (Roche Diagnostics, GmbH, Mannheim, Germany).
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7

Serum Biomarker Profiling: IL-6, CRP, TNF-aR1

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Non-fasting blood (serum) was drawn at baseline. Aliquots were stored, using customary secure procedures, at −70° C at both field centers. For this analysis, the following soluble protein biomarkers were measured: IL-6, CRP, and TNF-aR1. IL-6 was measured using a solid-phase immunometric assay on the IMMULITE 2000 (Siemens Healthineers). Assay detection was conducted via an enzyme-labeled, sequential assay in which a substrate was converted to the chemiluminescent product. The total imprecision of this method was acceptable as indicated by a 4-6% between-run coefficient of variation. High-sensitivity CRP (hsCRP) was measured using a Vista 1500 (Siemens Healthineers) by immunonephelometry in which polystyrene particles coated with monoclonal antibodies against human CRP aggregate with this protein in samples. The between-run imprecision (coefficient of variation) was typically 4 to 6%. TNF-aR1 was measured using a quantitative sandwich enzyme immunoassay (R&D Systems, Inc) where assay detection was colorimetric. Total imprecision of the runs was acceptable as indicated by a 3-4% between-run coefficient of variation.
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8

Assessing Acute Renal Failure Severity

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Acute renal failure was assessed 24 h after reperfusion by measuring the serum concentration of creatinine. Serum creatinine was measured enzymatically (Vista 1500, Siemens Healthcare, Erlangen, Germany). The renal tissue was embedded in formaldehyde. Four-micrometer sections were stained with periodic acid-Schiff reagents. Tubular injury was scored semi-quantitatively from zero to four by a blinded pathologist who examined at least 10 fields at ×200 magnification. Tubular injury was defined as a tubular dilatation, sloughing of tubular epithelial cells, or a naked tubular basement membrane. Only tubules in the outer stripe of the outer medulla (the most sensitive zone for ischemic injury) were included in the following scoring system: 0, no tubular injury; 1, < 20% of damaged tubules; 2, 21–50% of damaged tubules; 3, > 51% of damaged tubules; 4, total destruction of all epithelial cells [6 (link)].
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9

Comprehensive Iron Status Assessment

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Serum iron, ferritin, transferrin, CRP and soluble transferrin receptor (sTfR) and alpha-1 acid glycoprotein (AGP) were quantified using the Dimension RXL and Vista 1500 system (Siemens Healthcare, Saint-Denis, France). Transferrin saturation (TS) was calculated as the percent of (serum iron (µmol/L)/serum transferrin (g/L) × 25). The hemoglobin level was measured on an automated counter (Sysmex, Roissy, France), and quantification of IL-6 was performed using a cytometric bead array (BD Bioscience, Le Pont de Cliax, France).
Erythrocyte protoporphyrin was measured as previously described according to the European Porphyria Network guidelines [28 (link)].
Serum hepcidin was quantified by the previously published method of LC-MSMS [29 (link)].
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10

Hepatic Function Assessment in Mice

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Serum total bilirubin, serum alanine (ALT), and aspartate (AST) aminotransferase activities were determined by automated measurement (Vista 1500, Siemens Health Care Diagnostics Inc., Newark, Delaware, US) performed routinely at the biochemistry laboratory of the Edouard Herriot Hospital. As these hepatic functions are considered not to vary over time in WT mice [20] , serum ALT, AST, and bilirubin were assessed only at 20 weeks of age, whereas they were evaluated for each Atp7b -/-subgroup.
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