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Corticosterone elisa kit

Manufactured by Arbor Assays

The Corticosterone ELISA Kit is a quantitative in-vitro diagnostic test used to measure the concentration of corticosterone, a glucocorticoid hormone, in biological samples such as serum, plasma, urine, or cell culture supernatants. The kit utilizes a competitive enzyme-linked immunosorbent assay (ELISA) technique.

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4 protocols using corticosterone elisa kit

1

Saphenous Vein Blood Sampling for Corticosterone

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Blood was collected at around ZT 1 by saphenous venipuncture within 3 min of mouse cage handling. Mice were placed in a restrainer (a perforated 50-ml centrifuge tube), and their lateral saphenous vein was punctured using a 25-gauge needle. Blood (~50 μl) was collected into microcentrifuge tubes. Samples were left at room temperature for 30 min, then centrifuged for 8 min at 12,000 RPM. Serum was immediately stored at −80°C until analysis. Serum corticosterone was measured by a competitive immunoassay (Corticosterone ELISA Kit, Arbor Assays) following manufacturer’s protocol.
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2

Chicken Endocrine and Immune Markers

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Chicken CRH ELISA kit (Wuhan Colorful Gene Biotechnology Co., Ltd., JYM0155Ch), Corticosterone ELISA kit (Arbor Assays Co., Ltd., K014-H1), Chicken Tumor Necrosis Factor α (TNF-α) ELISA kit (Wuhan Colorful Gene Biotechnology Co., Ltd., JYM0033Ch), and Chicken Factor Related Apoptosis Ligand (FASL) ELISA kit (Shanghai Jianglai Biotechnology Co., Ltd., JL26226) were used to measure CRH, corticosterone, TNF-α and FasL, respectively, in serum and/or follicular fluid. The CRH detection range was 2 to 180 pg/mL (R > 0.92); the minimum level of corticosterone detection was 16.9 pg/mL; TNF-α detection range was 1.2 to 100 pg/mL (R > 0.92); and FasL detection range was 6.25 to 200 pg/mL. To start the measurement, 50 μL of standards or samples were added to wells of a microtiter plate. Then, after experimental procedures were performed in accordance with instructions of the respective kits, the plates were incubated at 37°C for 10 min (corticosterone was incubated at room temperature for 30 min). Finally, the optical density were read at 450 nm wavelength using a plate reader within 15 min after the reaction was terminated by adding 50 μL of the stop solution.
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3

Multiplex ELISA Profiling of Mouse Neonatal Plasma

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Mouse FABP4 (Mouse FABP4/A-FABP ELISA, RayBiotech), insulin (Insulin ELISA Mouse UltraSensitive, Mercodia), glucagon (Glucagon ELISA Human/Rat/Mouse, Mercodia), catecholamines (QuickDetect Catecholamine, Biovision), and corticosterone (Corticosterone ELISA Kit, Arbor Assays) concentrations were determined in mouse neonatal plasma samples using ELISAs according to the manufacturer’s instructions.
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4

Quantification of Corticosteroid Levels

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Serum and supernatant from oviduct homogenates were prepared as previously described (Zheng et al., 2016 (link)). Corticosterone concentrations were measured using corticosterone elisa kit (Arbor Assays, K014-H1), according to the manufacturer’s instructions. The minimum level of detection was 7.7 pg/ml, and the intra- and inter-assay CVs were <6.5% and <9.9%, respectively. Cortisol levels were measured by radioimmunoassay at the Central Hospital of Tai-An City using commercial kits (Wei-Fang (3 V) Bioengineering Co. Ltd., Wei-Fang city, China). The minimum level of detection was 0.15 ng/ml, and the intra- and inter-assay CVs were 5.3 and 6.7%, respectively.
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