{"product_id":"elk4071","title":"Human HBb(Hemoglobin Beta) ELISA Kit","description":"\u003cstrong\u003eAlternative Names:\u003c\/strong\u003e HB-B; HBD; CD113t-C; Beta Globin; Spinorphin\u003cbr\u003e\u003cstrong\u003eAssay Type:\u003c\/strong\u003e Competitive Inhibition\u003cbr\u003e\u003cstrong\u003eSensitivity:\u003c\/strong\u003e 2.82 pg\/mL\u003cbr\u003e\u003cstrong\u003estandard:\u003c\/strong\u003e 500 pg\/mL\u003cbr\u003e\u003cstrong\u003eDetection range:\u003c\/strong\u003e 7.82-500 pg\/mL\u003cbr\u003e\u003cstrong\u003eSample type:\u003c\/strong\u003e serum, plasma and erythrocyte lysates\u003cbr\u003e\u003cstrong\u003eAssay length:\u003c\/strong\u003e 2.5h\u003cbr\u003e\u003cstrong\u003eResearch Area:\u003c\/strong\u003e Hematology;\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 Human HBb protein. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human HBb. 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 Human HBb in the samples is then determined by comparing the OD of the samples to the standard curve.\u003cbr\u003e\u003cstrong\u003eUniProt ID:\u003c\/strong\u003e P68871","brand":"ELK Biotechnology","offers":[{"title":"96T","offer_id":50409861087512,"sku":"ELK4071","price":558.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0590\/5652\/1400\/files\/ELK_da45208f-8e63-4857-88f1-2422b9ccbddf.jpg?v=1751010326","url":"https:\/\/danabiosci.com\/products\/elk4071","provider":"Dana Bioscience","version":"1.0","type":"link"}