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Access estradiol assay

Manufactured by Beckman Coulter
Sourced in United States

The Access Estradiol Assay is a quantitative immunoassay used to measure the concentration of estradiol in human serum and plasma samples. It is designed for use on the Access family of immunoassay systems.

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3 protocols using access estradiol assay

1

Comprehensive Biomarker Analysis in Plasma

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Serum total cholesterol, triglyceride, low-density lipoprotein cholesterol (LDL), high-density lipoprotein cholesterol (HDL), fasting glucose, estradiol and follicle-stimulating hormone (FSH) were measured using standard procedures at the Department of Laboratory Medicine, Changhua Christian Hospital. Brief, the levels of estradiol and FSH were measured in frozen plasma specimens using the Access Estradiol assay and the Access hFSH assay on the Beckman Access Immunoassay system with a dynamic range of ≥ 3.5 logs (Beckman Coulter, Fullerton, CA.). Values for estradiol were reported as pg/ml and those for FSH were reported as mIU/mL. The lower limit value of detection was 20 pg/ml for estradiol and was 0.2 mIU/mL for FSH, respectively. The samples of estradiol and FSH were run undiluted. None of the others were outside the linear-range detection of standard curve. All samples were analyzed in duplicates. For quality control purposes, two duplicates of commercial control samples were tested on each microplate in any given run. The interassay and intraassay laboratory coefficients of variation (CVs) were < 8% and 8.6% for estradiol, respectively, and were < 8% and 5.6% for FSH, respectively. Insulin resistance was assessed based on the homeostatic model assessment of insulin resistance (HOMA-IR) using the following formula: [fasting glucose (mmol/L) × insulin (μU/L)/22.5].
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2

Measuring Hormones and Lipid Profiles

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The concentrations of follicle-stimulating hormone (FSH) and estradiol were measured according to the standard procedures of the Department of Laboratory Medicine, Changhua Christian Hospital. Briefly, we measured FSH and estradiol in plasma specimens using the Access hFSH Assay and the Access Estradiol Assay, respectively, on the Beckman Access Immunoassay System (Beckman Coulter, Fullerton, CA, USA). The unit measurement of FSH and estradiol was mIU/mL and pg/ml, respectively. For estradiol, the inter- and intra-assay laboratory coefficients of variation were less than 8% and 8.1%, respectively, and for FSH, they were less than 8% and 6%, respectively. We measured the levels of high-sensitivity C-reactive protein (hs-CRP) and total cholesterol (including low-density lipoprotein (LDL) cholesterol, high-density lipoprotein (HDL) cholesterol, and triglycerides (TG)) using an automatic lab instrument at the Department of Laboratory Medicine, Changhua Christian Hospital.
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3

Immunoassay for Plasma E2 and P4

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Plasma E2 and P4 concentrations were measured by paramagnetic particle and chemiluminescent immunoassay (Access Estradiol Assay and Access Progesterone Assay, respectively, Beckman Coulter, Inc.) using the Access Immunoassay Systems (Unicel Dxl 800 Access, Beckman Coulter, Inc.) according to the manufacturer's recommendations. The sensitivity of the E2 and P4 assays was 20 pg/mL and 0.10 ng/mL respectively. The total imprecision of E2 assay was ≤12% at concentrations ≥120 pg/mL. For P4 assay, the imprecision of within run and between run was ≤12% and ≤10% respectively.
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