3h
Human MINA(MYC Induced Nuclear Antigen) ELISA Kit
Human MINA(MYC Induced Nuclear Antigen) ELISA Kit
Assay length
Standard
10ng/mL
Assay Type
Sandwich
Sensitivity
0.056ng/mL
Detection range
0.156-10ng/mL
Research Area
Tumor immunity;
Test
ELISA Enzyme-linked immunosorbent assays Code 90320007 SNOMED
Alternative Names
MDIG; NO52; MINA53; ROX; Mineral dust-induced gene protein; Nucleolar protein 52; 60S ribosomal protein L27a histidine hydroxylase; Ribosomal oxygenase MINA
Description
Antigens are peptides or recombinant or native dependent on the production method.Induced protein genes, factors or kinases, increase the production of (an enzyme or other protein) at the level of genetic transcription.
Properties
E05 478 566 350 170 or Enzyme-Linked Immunosorbent Assays,E05 478 566 350 170 or Enzyme-Linked Immunosorbent Assays,Human proteins, cDNA and human recombinants are used in human reactive ELISA kits and to produce anti-human mono and polyclonal antibodies. Modern humans (Homo sapiens, primarily ssp. Homo sapiens sapiens). Depending on the epitopes used human ELISA kits can be cross reactive to many other species. Mainly analyzed are human serum, plasma, urine, saliva, human cell culture supernatants and biological samples.
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.