ELK4864-48T, Rat NES1(Nesfatin 1) ELISA Kit, 48T

ELK4864-48T, Rat NES1(Nesfatin 1) ELISA Kit, 48T

ELK4865-48T, Human PLOD2(Procollagen Lysine-2-Oxoglutarate-5-Dioxygenase 2) ELISA Kit, 48T

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ELK4864-96T, Rat NES1(Nesfatin 1) ELISA Kit, 96T

2.963,10 RON

Rat NES1(Nesfatin 1) ELISA Kit

SKU
ELK4864-96T

Alternative Names: Nesfatin-1

Species: Rat

Assay Type: Competitive Inhibition

Sensitivity: 182.5 pg/mL

Standard: 40000 pg/mL

Detection range: 625-40000 pg/mL

Sample type: Serum, plasma and other biological fluids

Assay length: 2h

Research Area: Glycolipid metabolism

Test principle: This assay employs the competitive inhibition enzyme immunoassay technique. The microtiter plate provided in this kit has been pre-coated with Rat NES1 protein. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Rat NES1. 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 NES1 in the samples is then determined by comparing the OD of the samples to the standard curve.

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Description

Alternative Names: Nesfatin-1

Species: Rat

Assay Type: Competitive Inhibition

Sensitivity: 182.5 pg/mL

Standard: 40000 pg/mL

Detection range: 625-40000 pg/mL

Sample type: Serum, plasma and other biological fluids

Assay length: 2h

Research Area: Glycolipid metabolism

Test principle: This assay employs the competitive inhibition enzyme immunoassay technique. The microtiter plate provided in this kit has been pre-coated with Rat NES1 protein. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Rat NES1. 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 NES1 in the samples is then determined by comparing the OD of the samples to the standard curve.