Human NBL1 (Neuroblastoma, Suppression Of Tumorigenicity 1) ELISA Kit

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 Neuroblastoma, Suppression Of Tumorigenicity 1(NBL1). Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody specific to Neuroblastoma, Suppression Of Tumorigenicity 1(NBL1). 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 Neuroblastoma, Suppression Of Tumorigenicity 1(NBL1), 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 Neuroblastoma, Suppression Of Tumorigenicity 1(NBL1) in the samples is then determined by comparing the OD of the samples to the standard curve.

Research Area: Tumor immunity

Alternative Names:
NB, DAN, NO3, DAND1, Differential Screening-Selected Gene Aberrant In Neuroblastoma, DAN domain family member 1

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

Assay Type: Sandwich

Standard: 10 ng/mL

Assay Length: 4.5h

Assay Length: For Research Use Only