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Porcine IFN-gamma ELISpot Kit

Porcine IFN-gamma ELISpot Kit

Catalogue No BSEK-330PO
Species Porcine
Size 96 T | 48 T
Price POR
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SKU: BSEK-330PO Categories: ,
Porcine IFN-gamma ELISpot Kit
PART DESCRIPTION
Microplate 96-well PVDF-backed microplate coated with a monoclonala ntibody
Detection Antibody Concentrate 120 uL of a 100X concentrated solution of biotinylated monoclonal antibody
Streptavidin-AP Concentrate A 120 μL of a 100X concentrated solution of Streptavidin con jugated to Alkaline Phosphatase with preservatives
Dilution Buffer 1 12 mL of a buffer for diluting Detection Antibody Concentra te with preservatives.
Dilution Buffer 2 12 mL of a buffer for diluting Streptavidin-AP Concentrate A with preservatives.
Wash Buffer Concentrate 20 mL of a 25X concentrated solution of a buffered surfact ant with preservative
Principle The enzyme-linked immunospot (ELISpot) assay was originally developed for the detection of individual B cells secreting antigen-specific antibodies. This method has since been adapted for the detection of individual cells secreting specific cytokines or other antigens. ELISpot assays employ the quantitative sandwich enzyme-linked immunosorbent assay (ELISA) technique. A monoclonal antibody specific for porcine IFN-γ has been pre-coated onto a PVDF (polyvinylidene difluoride)-backed microplate.Appropriately stimulated cells are pipetted into the wells and the microplate is placed into a humidified 37 °C CO2 incubator for a specified period of time. During this incubation period, the immobilized antibody in the immediate vicinity of the secreting cells binds secreted IFN-γ. After washing away any cells and unbound substances, a biotinylated monoclonal antibody specific for porcine IFN-γ is added to the wells. Following a wash to remove any unbound biotinylated antibody, alkaline-phosphatase conjugated to streptavidin is added. Unbound enzyme is subsequently removed by washing and a substrate solution (BCIP/NBT) is added. A blue-black colored precipitate forms at the sites of cytokine localization and appear as spots, with each individual spot representing an individual IFN-γ secreting cell. The spots can be counted with an ELISpot reader system or using a stereomicroscope.

For the quantitative determination of the frequency of cells releasing porcine Interferon gamma (IFN-γ).