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High Range Rat Insulin EIA
名称 High Range Rat Insulin EIA
型号
更新时间 2023-09-25
特点 High Range Rat Insulin EIA背景介绍:Mercodia High Range Rat Insulin ELISA provides a method for the quantitative determination of insulin in rat serum or plasma.}
  • 详细内容
品牌其他品牌货号10-1145-01
供货周期现货应用领域医疗卫生

High Range Rat Insulin EIA背景介绍: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 ß-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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