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Access analyzer

Manufactured by Beckman Coulter
Sourced in United States

The Access Analyzer is a fully automated clinical chemistry analyzer designed for high-throughput testing in medical laboratories. It performs a variety of immunoassay tests to aid in the diagnosis and monitoring of various health conditions.

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5 protocols using access analyzer

1

Comprehensive Laboratory Assessment Protocol

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Complete blood counts were measured with Unicel DxH800 Coulter Cell Analyzer (Beckman Coulter, USA) from K2EDTA samples. Serum LDH, creatinine, and ALT parameters were analyzed with AU 680 (Beckman Coulter, USA) spectrophotometrically. Ferritin levels were measured with a two-site immunoenzymatic assay in Access Analyzer (Beckman Coulter, USA). D-dimer parameter was quantitated with an immunoturbidimetric assay in 3.2% sodium citrated venous plasma (STA Compact, Diagnostica Stago, France). hs-CRP levels were measured nephelometrically (BN Prospec, Dade Behring, Germany). TSH, FT3, FT4, TPOAb, and TGAb parameters were measured by paramagnetic particle, chemiluminescent immunoassays in serum samples (DxI800, Beckman Coulter, USA). The reference range for TSH was 0.34–5.60 mU/L, for FT3 was 2.6–4.37 ng/L (0.061–0.103 pmol/L), and for FT4 was 0.61–1.12 ng/dl (0.144–0.26 pmol/L). TGAb was 0–115 IU/ml, and TPOAb was 0–34 IU/ml.
FSH and LH levels were also measured by paramagnetic particle, chemiluminescent immunoassays in serum samples (DxI800, Beckman Coulter, USA). Estradiol and testosterone levels were determined by electrochemiluminescence immunoassay (Modular Analytics E170, Roche Diagnostics, Germany).
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2

Serum Biomarkers in Prostate Cancer

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Patient serum was collected at the Mayo clinic on an Institutional Review Board–approved study of prospective biomarker collection. Patients enrolled were almost exclusively low and intermediate risk by NCCN criteria. Most patients were treated with EBRT as monotherapy. No patients underwent a radical prostatectomy. Serum specimens were collected, analyzed, and stored at baseline before the initiation of radiotherapy and at the first follow-up visit after treatment (3–7 months post-RT). Both serum PSA and free-PSA were measured utilizing the Hybritech assays on an Access analyzer (Beckman Coulter, Inc). Free-hK2 levels were measured utilizing a selective pair of monoclonal antibodies. The assay was implemented on the Access analyzer, and the cross-reactivity with PSA is negligible as previously described.(11 (link)) The hK2 limit of detection was 1.5 pg/mL and the day-to-day coefficient of variation set at <15%, was <4 pg/mL.
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3

Comprehensive Metabolic Profiling Protocol

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Blood concentration of fasting glucose, low and high density lipoprotein (LDL and HDL) cholesterol, and triglycerides was measured using commercially available kits on a Roche/Hitachi 912 (Roche Diagnostics, Switzerland). Insulin, C-reactive protein (CRP), apoliprotein-A1, and-B100 (Apo-A1 and Apo-B) levels were assessed using immunochemical methods and an Access Analyzer (Beckman Coulter, CA, USA). Creatinine was measured by Jaffè method, fibrinogen by Clauss method, and urea by a colorimetric method. Glycosylated hemoglobin (HbA1c) levels were measured in all subjects using an HPLC auto-analyzer Adams HA 8160 (Menarini, Italy). All these determinations were performed according to the manufacturer's specifications, and quality control was within the recommended precision for each test.
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4

Comprehensive Clinical Laboratory Analyses

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Complete blood counts were measured with a Unicel DxH800 Coulter Cell Analyzer (Beckman Coulter) from K2EDTA samples. Serum LDH, creatinine and ALT were analyzed spectrophotometrically with AU 680 (Beckman Coulter). Ferritin levels were measured with a two‐site immunoenzymatic assay in Access Analyzer (Beckman Coulter). The D‐dimer parameter was quantitated with an immuno‐turbidimetric assay in 3.2% sodium citrated venous plasma (STA Compact, Diagnostica Stago). Hs-CRP levels were measured with a nephelometric method (BN Prospec, Dade Behring). The electrochemiluminescence immunoassay method was used in the measurement of procalcitonin (Cobas e‐411 Analyzer, Roche Diagnostics).
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5

Startle Response and Cortisol Measurement

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At each assessment, participants were exposed to standardized 2-minute virtual reality scenes Startle responses were elicited by 40ms, 106dB white noise bursts during each scene, as well as in the presence of blank blue squares at a variable 15–45 sec interstimulus interval. They were measured using electromyography (EMG) of the orbicularis oculi muscle contraction using the EMG module of the Biopac MP150 system. Immediately before, immediately after, and 15 minutes after scene presentation, salivary cortisol samples were collected via Salivette (Sarsedt Inc, Newton, NC). Samples were immediately frozen and batch-processed using a chemiluminescent immunoassay on a Beckman Access analyzer. All samples were run in duplicate and 3 levels of quality control were processed in every assay. The detection limit for the salivary assay was 0.1 nmol/L. The inter-assay and the intra-assay coefficients of variations were under 10%.
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