Product Description
Human NIPA1(Non Imprinted In Prader Willi/Angelman Syndrome Region Protein 1) ELISA Kit is availabe at Gentaur for next week delivery.
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 Length: 4.5h
Research AreaResearch 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 then added to the appropriate microtiter plate wells 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.
