Human CERS1 ELISA KIT
Packing 96Tests
FOR RESEARCH USE ONLY; NOT FOR THERAPEUTIC OR DIAGNOSTIC APPLICATIONS! PLEASE READ ENTIRE PROCEDURE!
Gene Name CERS1
Protein Name Ceramide synthase 1
Alternative Name
Human CERS1 ELISA KIT ,Human LAG1 ELISA KIT ,Human EPM8 ELISA KIT ,Human LASS1 ELISA KIT ,Human UOG1 ELISA KIT ,Human ceramide synthase 1 ELISA KIT ,Human longevity assurance (LAG1 ELISA KIT ,Human S. cerevisiae)homolog 1 ELISA KIT ,Human longevity assurance gene 1 protein homolog 1 ELISA KIT ,Human protein UOG-1 ELISA KIT ,Human upstream of GDF1 ELISA KIT
Intended use
Human CERS1 ELISA KIT allows for the in vitro quantitative determination of CERS1 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 Human CERS1 ELISA KIT has been pre-coated with an CERS1 antibody specific to CERS1. Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody preparation specific for CERS1 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 CERS1, 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 CERS1 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