Blood specimens were harvested immediately after the diagnosis of PE was confirmed, or after a routine antenatal visit. Specimens of blood were centrifuged at 4000 revolutions per minute for 10 minutes and analyzed within 2 hours. Briefly, a Sysmex XN9000 hematology analyzer (Sysmex Corporation, Japan) was used for blood routine analysis. Fib, APTT, PT, and D-D levels were analyzed using a Werfen ACLTOP700 hematology analyzer (Werfen Corporation, Spain). In addition, we collected 5 mL of venous blood in a gold tube with a clot activator and gel, and the serum was collected to measure ALB, Cr, and Ca levels using a Cobas C702 automatic analyzer (Roche Corporation, Switzerland). FAR was determined by dividing the plasma Fib concentration by the serum ALB levels. In our clinical laboratory, all tests were performed in accordance with ISO15189.
Cobas c702 automatic analyzer
Manufactured by Roche
Sourced in Switzerland, Germany
The Cobas C702 is an automatic analyzer designed for clinical chemistry testing. It is capable of performing a wide range of diagnostic tests on blood, urine, and other biological samples. The Cobas C702 is a high-throughput instrument that can process multiple samples simultaneously, providing efficient and reliable results.
Automatically generated - may contain errors
Lab products found in correlation
3 protocols using cobas c702 automatic analyzer
1
Biomarker Analysis for Pulmonary Embolism
2
Fasting Serum Biomarker Profiling
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Venous samples were collected after a 12 h overnight fast and serum white blood cell (WBC) count, serum lipids, high-sensitivity C-reactive protein (hsCRP), hemoglobin A1C (HbA1C), and serum uric acid were examined. The biochemical tests were done using a Roche/Hitachi cobas c702 automatic analyzer (Roche Diagnostics) at the Department of Laboratory Medicine at Dongguk University Ilsan Hospital, which is accredited by the Korean Society for Laboratory Medicine and the Korean Association of Quality Assurance.
3
Cystatin C Assay Comparison
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The cysC value of each aliquot was simultaneously measured using the Gentiancys and Tina-quant Gen.2 assays (Rochecys; Roche, Mannheim, Germany), both on a Cobas c702 automatic analyzer (Roche). Each instrument was set based on the manufacturer’s recommendations and application notes. The Gentiancys calibrator (REF 1012, GentianAS) and Rochecys calibrator (C.f.a.s. Cystatin C, Roche) were standardized against the ERM-DA471/IFCC. The details of the cysC assay conditions are presented in Supplemental Data Table S1 .
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