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TNFB (bovine) AlphaLISA Detection Kit, 5,000 Assay Points

ITEM#: 2013-AL534F

MFR#: AL534F

The AlphaLISA immunoassay kit for detection and quantitation of bovine TNFa in serum, plasma, cell culture supernatants, and other sample types allows for fast, reproducible, and sensitive detection without the need for time-consuming wash steps or c

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The AlphaLISA immunoassay kit for detection and quantitation of bovine TNFa in serum, plasma, cell culture supernatants, and other sample types allows for fast, reproducible, and sensitive detection without the need for time-consuming wash steps or complicated assay development..Formats: Our HV (100 assay point) kits allow you to run 100 wells in 96-well format, using a 100 µL reaction volume (10 µL of sample). Our 500 assay point kit allows you to run 500 wells in 96-well or 384-well format, using a 50 µL reaction volume (5 µL of sample). Our 5,000 assay point kit allows you to run 5,000 wells in 96-well or 384-well format, using a 50 µL reaction volume (5 µL of sample). Features: No-wash steps, no separation steps ELISA alternative technology Sensitive detection Broad sample compati Small sample volume Results in less than 3 hours Half the time of an ELISA assayi> TNFa is a polypeptide hormone mainly produced by activated macrophages and T cells. It is one of the most powerful mediators of inflammation, either playing a beneficial or deleterious role in disease progression. In particular, TNFa plays a clinically-relevant role as a mediator of immune responses associated to mastitis, endotoxic shock and bovine tuberculosis caused by Mycoplasma bovis. The present kit permits detection of bovine TNFa (i.e. analyte) in bovine serum, plasma, and cell culture supernatants. AlphaLISA technology allows the detection of molecules of interest in a no-wash, highly sensitive, quantitative assay. In an AlphaLISA assay, a biotinylated anti-analyte antibody binds to the Streptavidin-coated Donor beads while another anti-analyte antibody is conjugated to AlphaLISA Acceptor beads. In the presence of the analyte, the beads come into close proximity. The excitation of the Donor beads causes the release of singlet oxygen molecules that triggers a cascade of energy transfer in the Acceptor beads, resulting in a sharp peak of light emission at 615 nm.