Mouse MKX ELISA KIT
Packing 96Tests
FOR RESEARCH USE ONLY; NOT FOR THERAPEUTIC OR DIAGNOSTIC APPLICATIONS! PLEASE READ ENTIRE PROCEDURE!
Gene Name MKX
Protein Name Homeobox protein Mohawk
Alternative Name
Mouse MKX ELISA KIT ELISA KIT ,Mouse Homeobox protein Mohawk ELISA KIT ELISA KIT ,Mouse C10orf48 ELISA KIT ELISA KIT ,Mouse IFRX ELISA KIT ELISA KIT ,Mouse IRXL1 ELISA KIT ELISA KIT ,Mouse iroquois homeobox protein-like 1 ELISA KIT ELISA KIT ,Mouse mohawk homeobox ELISA KIT ELISA KIT
Mouse MKX ELISA KIT Range 15.6-1000pg/mL
Intended use
Mouse MKX ELISA KIT allows for the in vitro quantitative determination of MKX concentrations in serum, plasma, tissue homogenates, cell culture supernates or other biological fluids.
| Reagent | Quantity |
| Assay plate | 1 |
| Standard | 2 |
| Sample Diluent | 1 × 20mL |
| Assay Diluent A | 1 × 10mL |
| Assay Diluent B | 1 × 10mL |
| Detection Reagent A | 1 × 120μL |
| Detection Reagent B | 1 × 120μL |
| Wash Buffer(25 x concentrate) | 1 × 30mL |
| Substrate | 1 × 10mL |
| Stop Solution | 1 × 10mL |
| Plate sealer | 5 |
Test principle
The microtiter plate provided in Mouse MKX ELISA KIT has been pre-coated with an MKX antibody specific to MKX. Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody preparation specific for MKX and then avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. Then a TMB substrate solution is added to each well. Only those wells that contain MKX, biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of a sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450 nm ± 2 nm. The concentration of MKX in the samples is then determined by comparing the O.D. of the samples to the standard curve.
Sample collection and storage
Serum - Use a serum separator tube (SST) and allow samples to clot for 30 minutes before centrifugation for 15 minutes at approximately 1000 × g. Remove serum and assay immediately or aliquot and store samples at -20
