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AlphaLISA Human and Rat IL-22 Detection Kit, 5,000 Assay Points

The AlphaLISA® Human/rat IL-22 Detection Kit is designed for detection and quantitation of human or rat interleukin 22 in cell culture media or serum using a homogeneous (no-wash steps, no separation steps) assay.

For research use only. Not for use in diagnostic procedures. All products to be used in accordance with applicable laws and regulations including without limitation, consumption & disposal requirements under European REACH regulations (EC 1907/2006).
Part Number: AL320HV
Unit Size:
Part Number: AL320C
Unit Size:
Part Number: AL320F
Unit Size:
  • 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).


    • 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

    IL22 is a member of a group of cytokines called the IL10 family (including IL19, IL20, IL24, and IL26), a class of potent mediators of cellular inflammatory responses. IL22, ~20 kDa in size, is produced by activated DC,TH1, TH17, and NK cells acting primarily on epithelial cells such as respiratory and gut epithelial cells.. On binding to its receptor (IL22R1), which is associated to the interleukin 10 receptor 2 (IL10R2), IL22 promotes activation of multiple signals including the STAT1, STAT3, ERK, p38, and JNK pathways. IL22 can contribute to immune disease through the stimulation of inflammatory responses, S100s and defensins. In some contexts, the pro-inflammatory versus tissue-protective functions of IL22 are regulated by the often co-expressed cytokine IL17A

    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.

  • Application
    Protein Analysis & Detection
    Assay Points
    Assay Target Class
    Automation Compatible
    Detection Method
    Experimental Type
    In vitro
    Quantity in a Package Amount
    1.0 Units
    Therapeutic Area