The AlphaLISA anti-PEG IgM Detection Kit is designed for the quantitative determination of anti-PEG IgM antibodies in sera using a homogeneous (no wash steps, no separation steps) assay.
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|Part Number||Unit Size||List Price||Your Price||Quantity|
|AL313HV||100 assay points||737.00 USD|
|AL313C||500 assay points||2758.00 USD|
|AL313F||5,000 assay points||16600.00 USD|
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The conjugation of small proteins, peptides, and oligonucleotides with polyethylene glycol (PEG), or PEGylation, has been shown to improve the pharmacokinetics of biological products by preventing their degradation, as well as improve tissue biodistribution and reducing immunogenicity and toxicity. However, there is an increasing body of data showing that PEG-conjugated compounds elicit IgG and IgM responses and anti-PEG antibodies also occur in 25% of healthy individuals. The presence of circulating anti-PEG antibodies may compromise the immunogenicity and limit the efficacy of therapeutic pegylated compounds. This AlphaLISA kit is designed to accurately measure levels of IgM anti-PEG antibodies in cell culture media, serum, and plasma.
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.
Disclaimer: For research use only. Not for use in diagnostic procedures.
|Assay Target||PEG IgM|
|Assay Target Class||Antibody|
|Experimental Type||In vitro|
|Product Brand Name||AlphaLISA|
|Shipping Condition||Blue Ice|
|Unit Size||5,000 assay points|
|Resource Type||File Name||File Format|
|Event||Society of Laboratory Automation & Screening (SLAS)||Event|