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. After fully centrifuged, all blood samples were stored at –80°C. Sandwich ELISA kits purchased from Elabscience (Wuhan, China) were used to measure serum SDF-1 levels. EZSACAN test During the test, patients placed their hands, feet and foreheads
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TPH-2 (OriGene Technologies Inc. Rockville, MD, USA) were assayed with a validated in-house ELISA as previously described in detail ( 9 ). Sera from healthy blood donors obtained from the Finnish Red Cross blood service served as reference. The cut
Department of Molecular Medicine and Surgery, Karolinska Institute, Stockholm, Sweden
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Department of Medicine, Karlstad Hospital, Karlstad, Sweden
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ranges were used to determine IGF-I SDS. Serum (S) suPAR was analysed using a commercial suPARnostic ELISA assay (ViroGates, Copenhagen, Denmark). All samples were analysed for S-suPAR at the same time and in the same batch with an interassay
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glucose (mmol/L)/22.5. Serum Nrg4 concentrations were measured using ELISA kits from Phoenix Pharmaceuticals Inc. (EK-056-24). Animal experiments Male C57BL/6 mice aged 8–10 weeks were housed at 22 ± 1°C with a humidity of 35 ± 5% under a 12-h
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A level Serum Sema 5A levels were measured with ELISA kits (SEL924Hu) according to the manufacturer’s instructions (CLOUD-CLONE CORP, Wuhan, China). The intra-assay CV value is less than 10% and the inter-assay CV value is less than 12
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at −80°C for testing. An ELISA was used for detecting the FGF21. The kit was provided by BIM Company (USA), and the detection was performed according to the manufacturer’s instructions. The serum insulin level was detected using a chemiluminescence
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determined by commercial ELISA kits following the manufacturer’s protocol (Jingmei Engineering, Jiangsu Province, China). For all kits, the interassay and intra-assay coefficients of variation were <12 and < 8%, respectively. The minimum detectable
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Department of Cardiology, Yanbian University Hospital, Yanji, China
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tissue wet weight (−80℃ was placed after anticoagulant treatment with aprotinin and EDTA in an ANP radioimmunoassay kit before collection of human, rat perfusate, and mouse plasma). ELISA Plasma from 163 patients was subjected to ELISA experiments
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collection All blood samples were collected from the abdominal aorta and immediately centrifuged at 3000 g for 10 min at 4°C under anesthesia before sacrifice. Serum IGF-1 levels were measured with ELISA kits (Cloud-Clone Corp., Wuhan, China) according
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former described pcD-ps vector with a removed poly-A fragment 3′ of the MSC-cloning region ( 9 ). The correctness of the mutant V2 receptor plasmids was verified by sequencing. For receptor detection by ELISA, wild-type (WT) and all mutant AVPR2-coding