Human NIPA1 (Non Imprinted In Prader Willi/Angelman Syndrome Region Protein 1) ELISA Kit | ELK5358

Human NIPA1 (Non Imprinted In Prader Willi/Angelman Syndrome Region Protein 1) ELISA Kit | ELK5358 | Gentaur UK, US & Europe Distribution

Alternative Names: FSP3; SPG6; Magnesium transporter NIPA1; Spastic Paraplegia 6 (Autosomal Dominant)

Species: Human

Assay Type: Sandwich

Sensitivity: 0.059 ng/mL

Standard: 10 ng/mL

Detection Range: 0.16-10 ng/mL

Sample Type: Tissue homogenates, cell lysates and other biological fluids

Assay Lenght: 3.5h

Research Area: Signal transduction

Test Principle: The test principle applied in this kit is Sandwich enzyme immunoassay. The microtiter plate provided in this kit has been pre-coated with an antibody specific to Non Imprinted In Prader Willi/Angelman Syndrome Region Protein 1 (NIPA1) . Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Non Imprinted In Prader Willi/Angelman Syndrome Region Protein 1 (NIPA1) . Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added, only those wells that contain Non Imprinted In Prader Willi/Angelman Syndrome Region Protein 1 (NIPA1), biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. 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 Non Imprinted In Prader Willi/Angelman Syndrome Region Protein 1 (NIPA1) in the samples is then determined by comparing the OD of the samples to the standard curve.