Research detection kit AlphaLISA®
for antigenslipidfor hepatitis B virus

research detection kit
research detection kit
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Characteristics

Applications
for research
Tested parameter
for antigens, lipid
Micro-organism
for hepatitis B virus
Sample type
blood, serum, plasma, cell
Analysis mode
ELISA
Sample volume

0.005 ml, 0.01 ml
(0.00017 US fl oz, 0.00034 US fl oz)

Description

The AlphaLISA® immunoDetection Kit for Hepatitis B Virus Surface antigen (HBsAg) enables the quantitative determination of HBsAg in cell culture media and buffer using a homogeneous AlphaLISA assay (no wash steps). Formats: Our 100 assay point kit allows you to run 100 wells in 96-well format, Our 500 assay point kit allows you to run 500 wells in 96-well or 384-well format, Our 5,000 assay point kit allows you to run 5,000 wells in 96-well or 384-well format, Features: No-wash steps, no separation steps ELISA alternative technology Sensitive detection Broad sample compatibility Small sample volume Half the time of an ELISA assay AlphaLISA technology allows the detection of molecules of interest in buffer, cell culture media, serum and plasma in a highly sensitive, quantitative, reproducible and user-friendly mode. In an AlphaLISA assay, a Biotinylated Anti-Analyte Antibody binds to the Streptavidin-coated Alpha 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 provokes 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. Hepatitis B surface antigen (HBsAg) is a protein from Hepatitis B virus (HBV). HBV circulates in infected blood when the virus is actively replicating. Infection with HBV induces a spectrum of clinical manifestations and chronic liver diseases. HBsAg can be found on the surface of the lipid envelope containing HBeAg. These antigens are recognized by antibody proteins which bind them.
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