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Standard biochemical kits

Manufactured by Pars Azmoon

Standard biochemical kits are a collection of reagents, solutions, and consumables designed for performing various biochemical analyses and experiments in a laboratory setting. These kits provide the necessary components to conduct tests, assays, and procedures related to the study of biological molecules, such as proteins, enzymes, and nucleic acids. The core function of these kits is to facilitate the reliable and consistent execution of established biochemical techniques, allowing researchers and laboratory professionals to obtain accurate and reproducible results.

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3 protocols using standard biochemical kits

1

Fasting Metabolic Biomarkers Measurement

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Venous blood samples were collected after 10–12 h of overnight fasting. Enzymatic colorimetric method was used to measure the levels of fasting blood glucose. Serum levels of Triglyceride (TG), Total Cholesterol (TC), and high-density lipoprotein (HDL) were calculated by the use of enzymatic assays and standard biochemical kits (Pars Azmun Co., Iran). Between- and within-run coefficient of variations were less than 6.2%. Low-density lipoprotein (LDL) was calculated by modified version of Friedewald equation (20 (link)). ECLIA method and Roche Diagnostics kits (Roche Cobas 6000 analyzer) were used to measure serum insulin. HOMA-IR (Homeostatic Model Assessment for Insulin Resistance) was calculated by the following equation: [fastinginsulin(μU/mLfastingglucose(mmol/L)]/22.5 (21 (link)). QUICKI (Quantitative Insulin Sensitivity Check Index) was computed as 1/[log(fastinginsulin[cpsbreak]inμU/mL)+log (fastingglucoseinmg/dL)] (22 (link)). TyG (Triglyceride and glucose) index was determined as Ln[TG(mg/dL)×fasting[cpsbreak]glucose(mg/dL)/2] (23 (link)).
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2

Biochemical Analysis of Breastmilk Composition

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The nutrient content of BM samples was also assessed using standard biochemical kits (Pars Azmoon, Tehran, Iran) for the total levels of protein, calcium, and triglyceride. All photometric analyses were performed at 37 °C using a plate reader (EpochTM, BioTek, Winooski, VT, USA). To evaluate all absorbance information, monochromatic readings were taken [36 (link)].
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3

Fasting Metabolic Biomarkers

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Patients were visited after an overnight fasting of 10–14 hours. Past medical history of patients was assessed. Patients’ sera were collected at the end of the experimental period to analysis biochemical parameters. Biochemical measurements of serum glucose, lipids, and glycated hemoglobin (HbA1c) were performed. Glucose was measured by glucose oxidase method kit (Pars Azmoon, Tehran, Iran). Serum total cholesterol and triglycerides were measured using standard biochemical kits (Pars Azmoon, Tehran, IR Iran). Blood glycated hemoglobin levels were measured by using Elisa kit (Bioassay technology laboratory, Elisa kit).
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