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Modular d2400

Manufactured by Hitachi
Sourced in Japan

The Modular D2400 is a versatile and reliable laboratory equipment designed for a variety of analytical applications. It features a modular construction that allows for customization and adaptation to specific research needs. The core function of the Modular D2400 is to provide accurate and precise measurements for scientific investigations.

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2 protocols using modular d2400

1

Blood Sample Collection and Analysis

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Following a 12-hour overnight fast, blood samples were obtained from the antecubital vein of each subject by venipuncture and were immediately centrifuged, aliquoted, and frozen at -20℃. The frozen serum and plasma samples were stored at -80℃ until analysis. Fasting serum glucose, total cholesterol, triglyceride, and HDL-cholesterol (HDL-C) levels were measured by enzymatic methods using a Hitachi Modular D2400 automated chemistry analyzer (Hitachi, Tokyo, Japan). Levels of low-density lipoprotein-cholesterol (LDL-C) were calculated using the following formula: LDL-C=total cholesterol-HDL-C-(triglyceride/5). Serum aspartate aminotransferase (AST) and alanine aminotransferase (ALT) levels were measured. Fasting insulin levels were measured using a chemiluminescent microparticle immunoassay (Abbott Architect system, Irving, TX, USA). Insulin resistance was estimated using the homeostatic model assessment of insulin resistance (HOMA-IR) and calculated using the following formula: HOMA-IR=[fasting insulin (µIU/mL)×fasting glucose (mg/dL)/18]/22.522) (link).
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2

Fasting Blood Sample Analysis Protocol

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After a 12-hour overnight fast, blood specimens were attained from the antecubital vein of the participants by venipuncture and were promptly centrifuged, aliquoted, and frozen at -20°C. The frozen serum and plasma samples were accumulated at -80°C until final analysis. Fasting plasma glucose, total cholesterol, triglyceride, and high-density lipoprotein-cholesterol (HDL-C) levels were quantified by enzymatic methods using a Hitachi Modular D2400 automated chemistry analyzer (Hitachi, Tokyo, Japan). Levels of low-density lipoprotein-cholesterol (LDL-C) were determined using the following equation: LDL-C=total cholesterol − HDL-C − (triglyceride/5). Fasting insulin concentrations were assessed using a chemiluminescent microparticle immunoassay (Abbott Architect System, Irving, TX, USA). We also subjected the fasting data to various transformations and ultimately defined quantitative insulin sensitivity check index (QUICKI=1/[log(I0)+log(G0)]), where I0 is the fasting insulin, and G0 is the fasting glucose. Insulin resistance was computed using the homeostatic model assessment of insulin resistance (HOMA-IR) and assessed using the following formula: HOMA-IR=(fasting insulin [μIU/mL]×fasting glucose [mg/dL]/18)/22.5 [16 (link)].
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