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Variant 2 hemoglobin a1c analyzer

Manufactured by Bio-Rad
Sourced in United States

The Variant II Hemoglobin A1c Analyzer is a laboratory instrument designed to measure the level of glycated hemoglobin (HbA1c) in human blood samples. It utilizes high-performance liquid chromatography (HPLC) technology to separate and quantify the different hemoglobin fractions, including HbA1c, which is an important biomarker for monitoring long-term blood glucose control in individuals with diabetes.

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2 protocols using variant 2 hemoglobin a1c analyzer

1

Diabetes Diagnostic Procedures Protocol

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Each patient underwent a physical examination that included measurements of height and weight. The body mass index was calculated as weight (kg) divided by height in meters squared (m2). Fasting venous blood sample was drawn on 6 a.m. after a 10‐h overnight fast to test the laboratory examinations. Fasting plasma glucose and 2‐h postprandial plasma glucose concentrations were immediately determined by the glucose oxidase method using the Hitachi 7600 autoanalyzer. HbA1c was assayed using high‐performance liquid chromatography (Variant II Hemoglobin A1c analyzer; Bio‐Rad Laboratories, Hercules, CA, USA), with inter‐ and intra‐assay CVs of <3.5 and <3.0%, respectively.
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2

Standardized Meal Test Protocol for Metabolic Markers

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Each subject had standardized meal tests at baseline and at the 12-week follow-up visit. Fasting blood samples were collected after an 8-hour overnight fast and postprandial blood was collected 2-hour later. The standard meal test was standardized instant noodles containing 69.3 g of carbohydrates, 9.3 g of protein, and 1.5 g of fat [15 (link)]. Blood pressure, height and waist were measured. BMI = weight (kg)/height(m)2.
Plasma glucose including fasting plasma glucose (FPG) and 2-h postprandial plasma glucose (2-h PG) levels were measured by glucose oxidase method. HbA1c was measured by using high-performance liquid chromatography with a VARIANT II Hemoglobin A1c analyzer (Bio-Rad Laboratories, Hercules, CA). Triglycerides (TG), total cholesterol (TC), high-density lipoprotein cholesterol (HDL-c), and low-density lipoprotein cholesterol (LDL-c) were determined by applying standard enzymatic methods using a biochemical analyzer (7600–120; Hitachi, Tokyo, Japan). The criteria for the serum sample included: 1) the volume of the serum sample was enough for the assay; 2) serum sample was stored properly. For fasting serum GDF15 levels, 51 of subjects from MET group and 53 subjects from ACA group were measured at the baseline and endpoint by quantitative sandwich enzyme-linked immunosorbent assay (R&D Systems, Minneapolis, USA).
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