| 名稱 | Ultrasensitive Mouse Insulin EIA |
| 型號 | |
| 更新時間 | 2023-09-25 |
| 特點 | Ultrasensitive Mouse Insulin EIA背景介紹：Mercodia Ultrasensitive Mouse Insulin ELISA provides a method for the quantitative determination of insulin in mouse serum or plasma.} |
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| 品牌 | 其他品牌 | 貨號 | 10-1249-01 |
|---|---|---|---|
| 供貨周期 | 現(xiàn)貨 | 應(yīng)用領(lǐng)域 | 醫(yī)療衛(wèi)生,化工 |
Ultrasensitive Mouse Insulin EIA背景介紹：
Mercodia Ultrasensitive Mouse Insulin ELISA provides a method for the quantitative determination of insulin in mouse serum or plasma.
Ultrasensitive Mouse Insulin EIA Summary and explanation of the test
Insulin is the principal hormone responsible for the control of glucose metabolism.It is synthesized in the ?-cells of the islets of Langerhans as the precursor,proinsulin, which is processed to form C-peptide and insulin. Both are secretedin equimolar amounts into the portal circulation. The mature insulin moleculecomprises two polypeptide chains, the A chain and the B chain. The two chainsare linked together by two inter-chain disulphide bridges. There is also an intrachain disulphide bridge in the A chain.?Secretion of insulin is mainly controlled by plasma glucose concentration,and the hormone has a number of important metabolic actions. Its principalfunction is to control the uptake and utilisation of glucose in peripheral tissuesvia the glucose transporter. This and other hypo-glycaemic activities, such as theinhibition of hepatic gluconeogenesis and glycogenolysis are counteracted by thehyperglycaemic hormones including glucagon, epinephrine (adrenaline), growthhormone and cortisol.
Ultrasensitive Mouse Insulin EIA Principle of the procedure
Mercodia Ultrasensitive Mouse Insulin ELISA is a solid phase two-site enzyme immunoassay. It is based on the direct sandwich technique in which twomonoclonal antibodies are directed against separate antigenic determinantson the insulin molecule. During incubation insulin in the sample reacts withperoxidase-conjugated anti-insulin antibodies and anti-insulin antibodiesbound to the microtitration well. A simple washing step removes unboundenzyme labeled antibody. The bound conjugate is detected by reaction with3,3’,5,5’-tetramethylbenzidine. The reaction is stopped by adding acid to give acolorimetric endpoint that is read spectrophotometrically.
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電話/傳真：13366128764
手機：15311648455
地址：北京市海淀區(qū)廂黃旗2號樓1層4-179室