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Jca bm9030

Manufactured by JEOL
Sourced in Japan

The JCA-BM9030 is a benchtop X-ray photoelectron spectrometer (XPS) designed for surface analysis. It provides high-resolution data on the elemental composition, chemical states, and depth profiling of solid sample surfaces.

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15 protocols using jca bm9030

1

Biochemical Markers of Biliary Damage

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Serum AST, ALT, and T-bil were measured using the standard spectrophotometric method with an automated clinical analyzer (JCABM9030; JEOL Ltd., Tokyo, Japan). The volume of bile sample was measured. LDH in bile samples were measured as an index of biliary damage,31 (link) by using the standard spectrophotometric method with an automated clinical analyzer (JCABM9030; JEOL Ltd., Tokyo, Japan).
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2

Cardiovascular Risk Factor Assessment

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Smoking and alcohol status; exercise habit; skipping breakfast; and history of dyslipidemia, diabetes, and hypertension were assessed using a self-reported questionnaire at each annual examination. BMI (kg/m2) was calculated from height and weight without shoes or heavy clothing. Blood pressure was measured in a sitting position. Blood samples were collected from the median cubital vein after an overnight fast and were measured for TC, LDL-C, TG, and HDL-C using automatic clinical chemistry analyzers (HITACHI 7250, 7600, 7700; Hitachi, Tokyo, Japan) and for blood glucose and HbA1c levels (JCA-BM9030; JEOL, Tokyo, Japan). The National Glycohemoglobin Standardization Program equivalent value (%) was used to convert the HbA1c value.25 (link)
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3

Serum Alanine Aminotransferase Measurement

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Serum alanine aminotransferase (sALT) levels in peripheral blood, an indicator of hepatocellular injury, were measured by a standard spectrophotometric method with an automated clinical analyzer (JCA‐BM9030; JEOL, Ltd., Tokyo, Japan).
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4

Measuring Serum ALT Levels

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Serum alanine aminotransferase (ALT) levels in peripheral blood, an indicator of hepatocellular injury, were measured using a standard spectrophotometric method with an automated clinical analyzer (JCA-BM9030; JEOL, Ltd., Tokyo, Japan).
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5

Hepatic Injury Biomarkers in Reperfusion

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Hepatic effluent was withdrawn at 10, 30, 60, 90, and 120 minutes of reperfusion and analyzed for aspartate aminotransferase (AST), alanine aminotransferase (ALT), and lactate dehydrogenase (LDH) levels with a standard spectrophotometric method with an automated clinical analyzer (JCA‐BM9030; JEOL, Ltd., Tokyo, Japan). Glutamate dehydrogenase (GLDH) was also measured as a parameter for mitochondrial injury upon reperfusion using a GLDH activity colorimetric assay kit (BioVision, Inc., Milipitas, CA). LDH leakage into the bile was determined as an index for biliary damage.30
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6

Measuring Liver Injury with sALT

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Serum alanine aminotransferase (sALT) levels, used as a measure of liver injury, were determined by a standard spectrophotometric method with an automated clinical analyzer (JCABM9030, JEOL Ltd.).
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7

Comprehensive Blood and Metabolic Panel

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White blood cell count, red blood cell count, hemoglobin, hematocrit, platelet count, total protein, albumin, total bilirubin, AST, ALT, LDH, γ-GTP, ALP, urea nitrogen, uric acid, creatinine, total cholesterol, HDL-Cholesterol, LDL cholesterol, triglyceride, sodium, potassium, chloride, HbA1c, and fasting blood glucose were measured. White blood cells, red blood cells, hemoglobin, hematocrit, and platelets were measured using Sysmex XE-2100 automated hematology analyzer (Sysmex, Kobe, Japan). Total protein, albumin, total bilirubin, AST, ALT, LDH, γ-GTP, ALP, urea nitrogen, uric acid, creatinine, total cholesterol, HDL-cholesterol, LDL cholesterol, triglyceride, sodium, potassium, and chloride were measured with LABOSPECT 008α (Hitachi High-Tech, Tokyo, Japan) and JCA-BM8060 (JEOL Ltd., Tokyo, Japan). HbA1c and fasting blood glucose levels were measured with JCA-BM9030 and JCA-BM9130 (JEOL Ltd., Tokyo, Japan).
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8

Cardiometabolic Risk Factor Assessment

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A questionnaire was used to assess smoking, alcohol, breakfast and physical activity habits, and history of dyslipidemia, hypertension, and diabetes at each annual examination. Height and weight were measured without shoes or heavy clothing, and body mass index (BMI) was calculated (kg/m2). Blood pressure was measured with the participant in a sitting position. Blood samples were collected after an overnight fast and measurements were made using automatic clinical chemistry analyzers (HITACHI 7250, 7600, and 7700; Hitachi, Tokyo, Japan) for triglyceride, low-density lipoprotein (LDL)-, and high-density lipoprotein (HDL)-cholesterol. Blood glucose and HbA1c levels were determined using an automated analyzer (JCA-BM9030; JEOL, Tokyo, Japan). The HbA1c value was converted to the National Glycohemoglobin Standardization Program equivalent value (%) using the following formula: HbA1c = 1.02 × HbA1c (Japan Diabetes Society) + 0.25.18 (link)
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9

Evaluating Hepatocellular Injury Markers

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The sALT level, an indicator of hepatocellular injury, was measured using a standard spectrophotometric method with an automated clinical analyzer (JCA-BM9030; JEOL Ltd.). Serum BHB was measured using an enzymatic method (ORIENTAL YEAST Co., Ltd.).
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10

Serum ALT Determination Protocol

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Serum ALT levels in peripheral blood, an indicator of hepatocellular injury, were determined using a standard spectrophotometric method with an automated clinical analyzer (JCA-BM9030; Jeol, Tokyo, Japan).
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