ELISA Kit for MYC Induced Nuclear Antigen (MINA)

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 0.056ng/mL

Sample type

Tissue homogenates, cell lysates 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 MYC Induced Nuclear Antigen (MINA). Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody specific to MYC Induced Nuclear Antigen (MINA). 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 MYC Induced Nuclear Antigen (MINA), 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 MYC Induced Nuclear Antigen (MINA) in the samples is then determined by comparing the O.D. of the samples to the standard curve.

Alternative Names

MDIG; NO52; MINA53; ROX; Mineral dust-induced gene protein; Nucleolar protein 52; 60S ribosomal protein L27a histidine hydroxylase; Ribosomal oxygenase MINA

Item Name

MYC Induced Nuclear Antigen

Research Area

Tumor immunity;

Reference