{"product_id":"elk2816","title":"Human PK2(Prokineticin 2) ELISA Kit","description":"\u003cstrong\u003eAlternative Names:\u003c\/strong\u003e PK-2; Bv8; MIT1; KAL4; Protein Bv8 Homolog\u003cbr\u003e\u003cstrong\u003eAssay Type:\u003c\/strong\u003e Competitive Inhibition\u003cbr\u003e\u003cstrong\u003eSensitivity:\u003c\/strong\u003e 95.3 pg\/mL\u003cbr\u003e\u003cstrong\u003estandard:\u003c\/strong\u003e 20000 pg\/mL\u003cbr\u003e\u003cstrong\u003eDetection range:\u003c\/strong\u003e 312.5-20000 pg\/mL\u003cbr\u003e\u003cstrong\u003eSample type:\u003c\/strong\u003e serum, plasma and other biological fluids\u003cbr\u003e\u003cstrong\u003eAssay length:\u003c\/strong\u003e 2.5h\u003cbr\u003e\u003cstrong\u003eResearch Area:\u003c\/strong\u003e Neuro science;\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 PK2 protein. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human PK2. 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 PK2 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 Q9HC23","brand":"ELK Biotechnology","offers":[{"title":"96T","offer_id":47539737755872,"sku":"ELK2816","price":558.0,"currency_code":"KRW","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0601\/9330\/8896\/files\/ELK_c58a5cf9-ed64-4fbb-8a64-84347acf54d0.jpg?v=1751005745","url":"https:\/\/rndmate.com\/products\/elk2816","provider":"알앤디메이트","version":"1.0","type":"link"}