{"product_id":"elk0251","title":"Rat 3-MH(3-Methylhistidine) ELISA Kit","description":"\u003cstrong\u003eAlternative Names:\u003c\/strong\u003e 3MH\u003cbr\u003e\u003cstrong\u003eAssay Type:\u003c\/strong\u003e Competitive Inhibition\u003cbr\u003e\u003cstrong\u003eSensitivity:\u003c\/strong\u003e 2.71 nmol\/mL\u003cbr\u003e\u003cstrong\u003estandard:\u003c\/strong\u003e 400 nmol\/mL\u003cbr\u003e\u003cstrong\u003eDetection range:\u003c\/strong\u003e 6.25-400 nmol\/mL\u003cbr\u003e\u003cstrong\u003eSample type:\u003c\/strong\u003e serum, plasma, tissue homogenates and other biological fluids\u003cbr\u003e\u003cstrong\u003eAssay length:\u003c\/strong\u003e 3.5h\u003cbr\u003e\u003cstrong\u003eResearch Area:\u003c\/strong\u003e Metabolism\u003cbr\u003e\u003cstrong\u003eTest principle:\u003c\/strong\u003e This assay employs the competitive inhibition enzyme immunoassay technique. The microtiter plate provided in this kit has been pre-coated with Rat 3-MH protein. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Rat 3-MH. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of Rat 3-MH in the samples is then determined by comparing the OD of the samples to the standard curve.","brand":"ELK Biotechnology","offers":[{"title":"96T","offer_id":47539480232160,"sku":"ELK0251","price":558.0,"currency_code":"KRW","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0601\/9330\/8896\/files\/ELK_cf421cda-d767-4dfc-b8d8-f4d67295244f.jpg?v=1750996639","url":"https:\/\/rndmate.com\/products\/elk0251","provider":"알앤디메이트","version":"1.0","type":"link"}