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Beckman synchron lx20

Manufactured by Beckman Coulter
Sourced in United States

The Beckman Synchron LX20 is a clinical chemistry analyzer designed for high-throughput testing in clinical laboratories. It provides automated analysis of a variety of clinical chemistry tests, including enzymes, electrolytes, and metabolites, using a range of sample types such as serum, plasma, and urine.

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30 protocols using beckman synchron lx20

1

Serum Bicarbonate Measurement in NHANES

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In the NHANES 1999 to 2000, serum bicarbonate concentrations were measured by a Hitachi Model 917 multichannel analyzer (Roche Diagnostics). Starting from the 2001 to 2006 cycle, serum bicarbonate concentrations were measured by a Beckman Synchron LX20 (Beckman Coulter Inc). Starting from the 2007 to 2008 cycle, serum bicarbonate concentrations were measured by a Beckman Synchron LX20 and Beckman UniCel DxC800 Synchron (Beckman Coulter Inc). Starting from the 2009 to 2014 cycle, serum bicarbonate concentrations were measured by a Beckman UniCel DxC800 Synchron (Beckman Coulter Inc). Starting from the 2015 to 2016 cycle, serum bicarbonate concentrations were measured by a Beckman UniCel DxC800 Synchron (Beckman Coulter Inc) and Beckman Coulter UniCel DxC 660i Synchron Access chemistry analyzer (Beckman Coulter Inc). Starting from the 2017 to 2018 cycle, serum bicarbonate concentrations were measured by a Roche Cobas 6000 Chemistry Analyzer (Roche Diagnostics Corp). The baseline concentration of bicarbonate in serum was measured at the baseline level of the study and analyzed according to the following clinically relevant stratification as categorical variables: low (< 22 mEq/L), normal (22-26 mEq/L), and high (> 26 mEq/L).
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2

Biochemical Analyses of Fructose, tPSA, and Zinc

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Analyses of fructose, tPSA, and zinc have been previously performed (n = 201, missing = 2) and described.20 (link) Briefly, fructose was measured with a spectrophotometric method (Beckman Synchron LX20, Brea, CA, USA) and the inter-assay CV was 5% (at 12.7 mmol l−1); tPSA was measured with the Delfia™ method (Wallac Oy, Turku, Finland) and the inter-assay CV was 12% (at 660 mg l−1); and zinc was measured with a colorimetric method (Beckman Synchron LX20) and the inter-assay CV was 7% (at 2.0 mmol l−1).20 (link)
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3

Biomarker Analyses in Fasted Blood

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Fasting blood samples were collected by a licensed phlebotomist and transported directly to the UCLA Clinical Immunology Research Laboratory (CIRL) for processing and storage at −80°C until analysis. C-reactive protein (CRP) and insulin testing was performed by the CIRL. Glucose, triglycerides, and high density lipoprotein- (HDL-) cholesterol testing was performed by the UCLA Clinical Laboratory.
Serum CRP was measured by a high-sensitivity sandwich enzyme immunoassay from Immundiagnostik. Interassay precision (expressed as percent coefficient of variation) ranged from 8.1% to 11.4% over a wide range of CRP concentrations. Plasma glucose was measured by the glucose oxidase method (measures oxygen consumption using an oxygen detecting electrode) on a Beckman Synchron LX20 automated system. Plasma insulin was measured by a sandwich immunoassay on the Siemens IMMUNLITE 2000 automated system. Serum triglycerides were measured on the Beckman Synchron LX20 automated system by a coupled enzymatic method that produces a red-colored complex. HDL-cholesterol was quantitated on the Beckman Synchron LX20 automated system using an elimination enzymatic assay from Polymedco. All tests were performed using the same lot of reagents or assay plates in order to minimize variability due to differences in reagent lots.
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4

Serum Iron, ALT, and AST Measurement

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According to the NHANES, a timed-endpoint method was used to measure serum iron level. Iron is released from transferrin by acetic acid and is reduced to the ferrous state. Then the ferrous ion is immediately complexed with the FerroZine Iron Reagent. The system monitors the changes in absorbance at 560 nm at a fixed-time interval and these changes in absorbance are proportional to the iron concentration in the samples. The Beckman Synchron LX20 or Beckman UniCel® DxC800 Synchron was used in 2003–2016, and the Roche Cobas 6000 (c501 module) analyzer was used in 2017–2018. Additionally, an enzymatic rate method or a kinetic rate method was used to measure the levels of serum ALT and AST using the Beckman Synchron LX20 or the Beckman UniCel® DxC800 Synchron in 2003–2018.
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5

Serum and Urinary Uric Acid Assessment

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After an overnight fast, venous blood samples were collected to assess serum uric acid and creatinine concentrations with standard (enzymatic and/or colorimetric) methods by an automatic analyzer [Beckman Synchron LX20; Beckman Coulter Inc., Brea California, USA or the Roche Cobase601 hs-cTnT assay (F Hoffmann-La Roche, Basel, Switzerland) on the Cobas 6000 analyzer for the last 2585 samples] at Maastricht University Medical Centre (The Netherlands).
To assess urinary uric acid and creatinine excretion, participants were requested to collect a 24-h urine sample. Participants were instructed both orally and in writing on the procedure concerning the 24-h urine collection. Only urine collections with a collection time between 20 and 28-h were considered valid, in case of violation participants were asked to collect urine once more. Urinary uric acid and creatinine concentration were measured with a standard immunoturbidimetric assay by an automatic analyzer (Beckman Synchron LX20; Beckman Coulter Inc.) and multiplied by collection volume to obtain the 24-h urinary uric acid excretion. According to the DuBois and DuBois equation, 24-h urinary uric acid and creatinine excretion were adjusted for body surface [14] .
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6

Uric Acid and Bone Mineral Density

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The principal variables of this study were sUA (independent variable) and total BMD (dependent variable). SUA levels were measured using a Hitachi Model 917 multichannel analyser (Roche Diagnostics, Indianapolis, IN) from 1999 to 2001 and a Beckman Synchron LX20 (Beckman Coulter, Inc., Brea, CA) in 2002. Distributions of UA results from the two laboratories were compared at the time of transition, and no significant differences were observed. Total BMD was measured by dual-energy X-ray absorptiometry.
In addition, the following covariates were included: age, sex, race/ethnicity, BMI, income-poverty ratio, physical activity, blood urea nitrogen, total protein, total cholesterol, serum phosphorus, and serum calcium. Details of sUA and total BMD measurement process and other covariate acquisition process are available at www.cdc.gov/nchs/nhanes/.
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7

Demographic Factors and Biomarker Analysis

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In-person interviews were used to collect demographic factors, such as age, gender, race, cigarette smoking status, and previous medical history. The race and ethnicity of participants were classified as Hispanic, non-Hispanic Black, non-Hispanic White, non-Hispanic Asian, and others. Participants were asked “Do you now smoke cigarettes?” to determine cigarette smoking use. Medical history was obtained from a self-reported questionnaire, including coronary heart disease, angina pectoris, and liver condition. Body mass index (BMI) was estimated by dividing the weight (kg) by the square of height (m) (kg/m2). Height was estimated using a portal stadiometer, a digital measurement device connected to the acrylic headpiece and interfaced directly with the NHANES Integrated Survey Information System (ISIS) anthropometry application. Weight was estimated using a portal digital weight scale, which was a high-performance instrument linked directly to the ISIS anthropometry application. Serum calcium concentration was analyzed using Beckman Synchron LX20 (Beckman Coulter, Brea, CA). Laboratory biochemical data included glucose, alanine aminotransferase, platelet, creatinine, high density-lipoprotein cholesterol, and C-reactive protein, which were collected by trained medical technologists using standard procedures.
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8

Antibody Synthesis and Biochemical Assays

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α1-R Ab was synthesized and donated by Huazhong University of Science and Technology, as previously described (31 ) and streptozotocin (STZ; cat. no. S0130) was purchased from Sigma-Aldrich (Merck KGaA, Darmstadt, Germany). Rabbit anti-mouse TGF-β1 (cat. no. BA0290), immunohistochemical streptavidin-biotin complex (SABC) kits (cat. no. SA1025) and diaminobenzidine (DAB) colorant (cat. no. AR1022) were obtained from Boster Systems, Inc. (Plesanton, CA, USA). A glucose assay kit (Glucose Oxidase Peroxidase; cat. no. F006) was purchased from the Nanjing Jiancheng Bioengineering Institute (Nanjing, China). A urinary albumin kit (cat. no. A028-1) for use in a radioimmunoassay was obtained from Beijing Furui Bioengineering Co., Ltd. (Beijing, China) and a serum creatinine (Scr) kit (cat. no. C011-2) was purchased from Nanjing Jiancheng Bioengineering Institute for use with a Beckman Syn Chron-LX20 full-automatic biochemical analyzer (Beckman Coulter, Inc., Brea, CA, USA). FEI Tecnai G2 20 TWIN electron microscopes were provided by the Wuhan Institute of Virology at the Chinese Academy of Sciences (Wuhan, China).
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9

Comprehensive Metabolic Profile Assessment

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Blood was obtained through capillary blood collection; fasting blood glucose (FBG) was examined instantly using the One-Touch FreeStyle Freedom Lite blood glucose monitor (Abbott Diabetes Car Inc., CA, USA). Blood biomarkers, such as insulin, triglycerides, total cholesterol (TC), aspartate transaminase (AST), alanine transaminase (ALT), creatinine, blood urea nitrogen (BUN), uric acid, high-sensitivity C-reactive protein (hs-CRP), and LDL-C, and high-density lipoprotein-cholesterol (HDL-C), were analyzed from a 4-mL blood sample by using the Beckman Synchron LX-20 (Beckman Coulter Inc., CA, USA). Glycated hemoglobin (HbA1c) levels were analyzed from another 1.5-mL blood sample by using Spotchem SP-4410 (Arkray Inc., Kyoto, Japan). All the listed experiments and procedures were performed in the authorized Yea-Tong laboratory center, in Chung-Li City, Taiwan.
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10

Birth Cohort and ALT Levels for Anti-HCV Testing

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Participants’ birth year and ALT levels were selected as the variables for evaluation of anti-HCV testing strategies. Birth year was estimated by subtracting participant age at time of survey from the estimated year in which the participant was surveyed.51 (link) Persons with birth year 1945–1965 were classified as being within the birth cohort. Elevated ALT was defined as ≥40 IU/L based on a one-time measurement of serum ALT activity (Hitachi 917, Roche Diagnostics, Indianapolis IN [1999–2001]; Beckman Synchron LX20 and DxC800, Beckman Coulter, Inc., Fullerton CA [2002–2008]). The analytic sensitivity and range of the different analyzers were similar and the distributions of ALT activity did not differ significantly.52 (link)–58
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