Product Overview:
The mouse interleukin 1 beta (IL-1β) ELISA assay kit (enzyme-linked immunoassay kit) is intended for the quantitative determination of mouse interleukin 1 beta (IL-1β) concentrations in cell culture supernates, serum, and plasma.
Assay Principle:
The mouse interleukin 1 beta (IL-1β) ELISA employs the quantitative sandwich enzyme immunoassay technique. A monoclonal antibody specific for iterleukin 1 beta (IL-1β) has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and any interleukin 1 beta (IL-1β) present is bound by the immobilized antibody. Following incubation unbound samples are removed during a wash step, and then a detection antibody specific for Interleukin 1 Beta (IL-1β) is added to the wells and binds to the combination of capture antibody-IL-1β in sample. Following a wash to remove any unbound combination, and enzyme conjugate is added to the wells. Following incubation and wash steps a substrate is added. A colored product is formed in proportion to the amount of interleukin 1 beta (IL-1β) present in the sample. The reaction is terminated by addition of acid and absorbance is measured at 450nm. A standard curve is prepared from seven interleukin 1 beta (IL-1β) standard dilutions and Interleukin 1 Beta (IL-1β) sample concentration determined.
Dynamic Range:
31.25 – 2000 pg/ml
Incubation Time:
3.5 hours
Sample Type:
Cell culture, serum, plasma
Specimen Collection and Handling:
Cell culture supernates – remove particulates by centrifugation.
Serum – use a serum separator tube (SST) and allow samples to clot for 30 minutes before centrifugation for 15 minutes at approximately 1000 x g. Remove serum, avoid hemolysis and high blood lipid samples.
Plasma – recommended EDTA as an anticoagulant in plasma. Centrifuge for 15 minutes at 1000 x g within 30 minutes of collection.
Assay immediately or aliquot and store samples at -20°C. Avoid repeated freeze-thaw cycles.
Dilute samples at the appropriate multiple (recommended to do pre-test to determine the dilution factor).