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      High Range Rat Insulin EIA
      名稱(chēng) High Range Rat Insulin EIA
      型號
      更新時(shí)間 2023-09-25
      特點(diǎn) High Range Rat Insulin EIA背景介紹:Mercodia High Range Rat Insulin ELISA provides a method for the quantitative determination of insulin in rat serum or plasma.}
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      品牌其他品牌貨號10-1145-01
      供貨周期現貨應用領(lǐng)域醫療衛生

      High Range Rat Insulin EIA背景介紹:Mercodia High Range Rat Insulin ELISA provides a method for the quantitativedetermination of insulin in rat serum or plasma.


      High Range Rat Insulin EIA Summary and explanation of the test

      Insulin is the principal hormone responsible for the control of glucose metabolism.It is synthesised 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.


      High Range Rat Insulin EIA  Principle of the procedure

      Mercodia High Range Rat Insulin ELISA is a solid phase two-site enzymeimmunoassay. 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 a colorimetric endpoint that is read spectrophotometrically。

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