ELISA Kit for Macrophage Inflammatory Protein 1 Gamma (MIP1g)

Format

48T, 96T, 96T×5, 96T×10, 96T×100

Detection range

15.6-1,000pg/mL

Application

Enzyme-linked immunosorbent assay for Antigen Detection.

Organism species

Rattus norvegicus (Rat)

Sensitivity

The minimum detectable dose of this kit is typically less than 6.0pg/mL

Sample type

Serum, plasma, tissue homogenates, cell lysates, cell culture supernates 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 Macrophage Inflammatory Protein 1 Gamma (MIP1g). Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody specific to Macrophage Inflammatory Protein 1 Gamma (MIP1g). 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 Macrophage Inflammatory Protein 1 Gamma (MIP1g), 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 Macrophage Inflammatory Protein 1 Gamma (MIP1g) in the samples is then determined by comparing the O.D. of the samples to the standard curve.

Alternative Names

CCL9; CCL10; SCYB9; CCF18; MRP2; C-C motif chemokine 9; Macrophage inflammatory protein-related protein 2; Small-inducible cytokine A9

Item Name

Macrophage Inflammatory Protein 1 Gamma

Research Area

Cytokine;Infection immunity;Human gene deletion;

Reference