AlphaLISA Mutant Ataxin 2 Detection Kit, 100 Assay Points

The ATXN2 gene encodes the RNA-binding protein called Ataxin 2. When bearing lengthy polyglutamine tracts, Ataxin 2 causes neurodegeneration, which speeds up the onset of ALS illness. According to recent research in neurodegenerative diseases, TDP-43 regulates the expression of Ataxin 2, and in cellular and animal models, Ataxin 2 changes the toxicity of TDP-43. New research indicates that reduced Ataxin 2 levels prevent TDP-43 aggregation, suggesting that future therapy efforts should investigate both proteins in tandem.

Formats

• Our 100 assay point kit allows 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 compatibility
• Small sample volume
• Results in less than 3 hours
• Half the time of an ELISA assay

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.