ELISA Kit for Paraneoplastic Antigen MA2 (PNMA2)

Format

48T, 96T, 96T×5, 96T×10, 96T×100

Detection range

0.156-10ng/mL

Application

Enzyme-linked immunosorbent assay for Antigen Detection.

Organism species

Homo sapiens (Human)

Sensitivity

The minimum detectable dose of this kit is typically less than 0.058ng/mL

Sample type

Tissue homogenates and other biological fluids.

Assay length

3h

Method

Double-antibody Sandwich

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 Paraneoplastic Antigen MA2 (PNMA2). Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody specific to Paraneoplastic Antigen MA2 (PNMA2). 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 Paraneoplastic Antigen MA2 (PNMA2), 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 Paraneoplastic Antigen MA2 (PNMA2) in the samples is then determined by comparing the O.D. of the samples to the standard curve.

Alternative Names

Ma2/Ta; Ma2Ta; RGAG2; Autoantigen Ta; 40 kDa neuronal protein; Onconeuronal antigen Ma2; Paraneoplastic neuronal antigen MM2

Item Name

Paraneoplastic Antigen MA2

Research Area

Tumor immunity;

Reference