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Elecsys estradiol 2

Manufactured by Roche
Sourced in United States

The Elecsys Estradiol II is a laboratory equipment product developed by Roche. It is an immunoassay used for the quantitative determination of estradiol in human serum and plasma. The Elecsys Estradiol II provides a fully automated solution for the measurement of estradiol levels.

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3 protocols using elecsys estradiol 2

1

Adrenal Hormone Profiling in Fasting Blood

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We collected fasting venous blood samples for measurement of adrenal androgens such as testosterone (normal range, 3–10 ng/dL), dehydroepiandrosterone (DHEA) (normal range, 20–275 ng/dL), androstenedione (normal range, 8–50 ng/dL), and estradiol (normal range lower than 1.5 ng/dL). Testosterone (KIP1709; DIAsource ImmunoAssays S.A., Nivelles, Belgium), DHEA (IMaa38; IMMUNOTECH, Marseille, France), and androstenedione (KIP0451; DIAsource ImmunoAssays, S.A., Louvain-la-Neuve, Belgium) were measured using commercial kits.
The estradiol level in blood was measured only in female subjects (n = 94) by using a competitive electrochemiluminescence immunoassay method with an Elecsys E170 analyzer (Elecsys Estradiol II; Roche Diagnostics GmbH, Mannheim, Germany).
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2

Serum Estradiol Levels After Ovariectomy

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Blood samples were obtained by venipuncture of the tail under 1% isoflurane anaesthesia before bilateral ovariectomy, before the 1st acid injection (3 weeks post-surgery), and at day 14 after the 2nd acid injection (6 weeks post-surgery). The serum concentration of the unconjugated form of 17β-oestradiol was measured with a commercially available electrochemiluminescence immunoassay (ECLIA) kit “Elecsys Estradiol II” (Roche Diagnostics, Indianapolis, IN, USA). The detection limit is 5 pg/mL for ECLIA. Values below the detection limit were arbitrarily deemed 5 pg/mL for the statistical analysis.
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3

Endocrine and Metabolic Biomarker Assessment

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All clinical variables of the study participants were assessed when they first visited the outpatient department. Blood samples for biochemical laboratory analyses were taken from all subjects in the early follicular phase after overnight fasting. Serum E1 was measured using the Dsl-8700 Estrone ELISA kit (Beckman Coulter, Brea, CA, USA) and serum E2 was measured using Elecsys Estradiol II (Roche, Indianapolis, IN, USA) [23 (link)]. Serum insulin and glucose levels were analyzed using an Elecsys Insulin assay (Roche) and an L-Type GluI device (Wako, Osaka, Japan), respectively. Cholesterol and triglyceride levels were measured using Pureauto S (Sekisui, Tokyo, Japan), and serum high-density lipoprotein and low-density lipoprotein levels were measured using Cholestest (Sekisui) [30 (link)]. Both intra- and inter-assay coefficients of variation for all assays were below 8%.
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