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Au2700 automatic biochemistry analyzer

Manufactured by Olympus
Sourced in Japan

The AU2700 is an automatic biochemistry analyzer designed for clinical laboratory testing. It performs quantitative analysis of various biochemical components in biological samples, such as blood, urine, or other bodily fluids. The analyzer utilizes spectrophotometric techniques to measure the concentrations of specific analytes.

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6 protocols using au2700 automatic biochemistry analyzer

1

Unilateral Renal Ischemia-Reperfusion Injury in Rats

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Clean, healthy male SD rats were purchased from Jinan Yuepeng Animal Center, weighing approximately 150–180 g. Forty SD rats were adaptively fed for one week and then randomly divided into the following 6 groups: control group, after AKI 1-day group (AKI 1D), after AKI 1-week group (AKI 1W), after AKI 2-week group (AKI 2W), after AKI 4-week group (AKI 4W), and after AKI 8-week group (AKI 8W). After being anesthetized, the right kidneys of all experimental rats were removed, and the left renal pedicles were closed with non-invasive vascular clamp for 40 min and then unclamped. During this process, we observed that the kidney color gradually changed from bright red to dark red, and then rapidly from dark red to bright red after unclamped. The left kidney of the control group was not clipped. We collected 2 ml of blood from the rat heart and removed the left kidneys at different time after the operation. The levels of serum creatinine (Scr) were detected by Olympus AU2700 automatic biochemistry analyzer.
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2

Physiological Responses to Simulated High Altitude

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To verify the responses of rats after exposure to high altitudes, capillary oxygen saturation (ScO2) was measured using a TuffSat TTM Oximeter (GE-Datex Ohmeda, United States). A routine blood examination contains red blood cells, white blood cells, hemoglobin, lymphocyte levels, granulocyte, and platelet count were determined with an XFA6100 automatic hematology analyzer (Nanjing Perlove Medical Equipment, Co., Ltd., China). Blood biochemical parameters comprises ScO2, alanine aminotransferase, aspartate aminotransferase, total bilirubin, total protein, albumin, glutamate, total cholesterol, and globulin were examined by an AU2700 automatic biochemistry analyzer (Olympus Corporation, Japan) in rats after exposure to simulated high altitude hypoxia.
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3

Hematological and Biochemical Analysis of X-Ray Irradiated Rats

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A routine blood examination was performed with an XFA6100 automatic hematology analyzer (Nanjing Perlove Medical Equipment, Co., Ltd., China), and blood biochemical parameters were determined by applying an AU2700 automatic biochemistry analyzer (Olympus Corporation, Japan) to rats after exposure to X-ray irradiation.
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4

Contrast-Induced Nephropathy Biomarkers

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SCr and other biochemical indicators were measured. Fasting blood specimens were collected prior to and at 24 and 48 h after the procedure in the biochemical laboratory and subjected to analysis using an Olympus AU2700 Automatic Biochemistry Analyzer (Olympus, Center Valley, PA, USA) for determination. Urine specimens were collected prior to and at 2, 6, 12, 24 and 48 h after the procedure and immediately centrifuged (1,409 × g, 20 min, 4°C). The supernatant fractions were collected and stored frozen at −80°C until use. Urinary levels of IL-18 were measured using an ELISA kit purchased from R&D Systems (Minneapolis, MN, USA). All procedures were performed strictly following the manufacturer’s instructions. Renal function was assessed by the eGFR using the Modification of Diet in Renal Disease formula for Chinese patients (8 (link)): GFR (ml/min/1.73 m2) = 175 × SCr (mg/dl)−1.1549 × age−0.2039 (x 0.79 if female). This equation gives a more accurate assessment of renal function than SCr alone. CIN was defined as an increase of ≥0.5 mg/dl or ≥25% in SCr concentration over baseline 24–48 h after the intravascular administration of contrast medium, without an alternative etiology (9 (link)).
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5

Biomarker Profiling in Acute Decompression Illness

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Blood samples from the vein were taken from the patients within 24 hours of DEACMP onset. White blood cell (WBC) count was measured using an automatic blood cell analyzer (Sysmex, Kobe, Japan). The serum was separated by centrifugation at 2500 g for 15 min. The serum level of COHb was measured using a pulse co-oximeter (Masimo Rad-7, Masimo, Irvine, CA, USA), cTnI using a chemiluminescent immunoassay on Access 2 analyzer (Beckman Counter, Brea, California, USA), Lac using a Cobas 6000 analyzer (Roche Diagnostics GmbH, Mannheim, Germany), CK by a colorimetric method using a creatine kinase activity assay kit (Abcam, Cambridge, MA, USA), CKMB isoenzyme using a Beckman CX3 automatic biochemistry analyzer (Hitachi, Tokyo, Japan), LDH using an AU 2700 automatic biochemistry analyzer (Olympus, Tokyo, Japan), NSE using a solid-phase immunoassay with double monoclonal antibodies with an Elecsys 2010 (Roche Diagnostics GmbH, Germany), and CRP using a turbidity method based on latex agglutination on a CRP-Latex (II) X2 reagent Hitachi 7020 analyzer (Hitachi, Tokyo, Japan).
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6

Comprehensive Blood Analysis in Rats

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Venous blood was collected from all rats, and red blood cells (RBC), white blood cells (WBC), and hemoglobin (HGB) were determined using an XFA6100 automatic hemocyte analyzer (Perlong Medical Inc, China). Blood oxygen saturation (ScO2) was measured using a TUFFSAT oximeter (Ohmeda medicalMedical Inc, USA). Albumin (ALB) and bilirubin (BIL) were determined by an AU2700 automatic biochemistry analyzer (Olympus Inc, Japan).
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