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Human eia kit

Manufactured by Phoenix Pharmaceuticals
Sourced in United States

The Human EIA Kit is a laboratory equipment product designed for the measurement of analytes in human samples. It provides a standardized and reliable method for quantitative analysis. The kit includes necessary reagents and components to perform the enzyme-linked immunosorbent assay (EIA) technique.

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2 protocols using human eia kit

1

Insulin Resistance and Myokine/Adipokine Levels

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Patient medical history and clinical characteristics were collected from medical records. Fasting blood was analyzed to determine glucose (GLU), glycosylated hemoglobin (HbA1c), and immunoreactive insulin (IRI) levels. We evaluated the endogenous effect of insulin resistance on vascular function. Insulin resistance was assessed using the homeostasis model assessment of insulin resistance (HOMA-IR). HOMA-IR was calculated as follows: HOMA-IR = (IRI × fasting plasma GLU) / 405. Additionally, we measured the plasma levels of myokines, adiponectin, leptin, and irisin. Blood samples were stored at − 80 °C, and both myokine and adipokine levels were measured according to the manufacturer’s instructions. Serum myostatin and irisin levels as myokines were measured using the GDF-8/Myostatin Quantikine ELISA Kit (R&D Systems, Minneapolis, MN, USA) and human EIA Kit (Phoenix Pharmaceuticals Inc., Burlingame, CA, USA). Serum adiponectin and leptin levels as adipokines were measured using the human Quantikine ELISA Kit (R&D Systems, respectively. Minneapolis, MN, USA). The intra- and inter-assay coefficients of variation were 2.5–4.7% and 5.8–6.9% for adiponectin, 3.0–3.3% and 3.5–5.4% for leptin, 1.8–5.4% and 3.6–6.0% for myostatin, and < 10% and < 15% for irisin, respectively.
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2

Metabolic Biomarker Profiling in Women

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Although this study included premenopausal and postmenopausal women, the timing of blood collection was not determined by the menstrual cycle. Fasting blood samples were collected for determining the serum levels of triglycerides, HDL cholesterol, LDL cholesterol, plasma glucose, HbA1c, C-reactive protein (CRP), and immunoreactive insulin (IRI). Homeostasis model assessment of insulin resistance (HOMA-IR) was calculated based on the blood insulin level after fasting early in the morning [HOMA-IR = (IRI × fasting plasma glucose)/405].
Blood samples were stored at −80°C, and both adipokine and myokine levels were measured according to the manufacturer’s instructions. Serum adiponectin and leptin levels as adipokines were measured using the human Quantikine ELISA Kit (R&D Systems, Minneapolis, MN, USA). Serum myostatin and irisin levels as myokines were measured using the GDF-8/Myostatin Quantikine ELISA Kit (R&D Systems, Minneapolis, MN, USA) and human EIA Kit (Phoenix Pharmaceuticals Inc., Burlingame, CA, USA), respectively. The intra- and inter-assay coefficients of variation were 2.5–4.7% and 5.8–6.9% for adiponectin, 3.0–3.3% and 3.5–5.4% for leptin, 1.8–5.4% and 3.6–6.0% for myostatin, and < 10% and < 15% for irisin, respectively.
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