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The ELISPOT assay is designed to enumerate cytokine producing cells in a single cell suspension. This method has the advantage of requiring a minimum of in-vitro manipulations allowing cytokine production analysis as close as possible to in-vivo conditions in a highly specific way. This technique is designed to determine the frequency of cytokine producing cells under a given stimulation, and the follow-up of such frequency during a treatment and/or a pathological state. Elispot assay constitutes an ideal tool in the TH1 / TH2 response, vaccine development, viral infection monitoring and treatment, cancerology, infectious diseases, autoimmune diseases and transplantation.
Abcam Elispot assay is based on sandwich immuno-enzyme technology. Cell secreted cytokines or soluble molecules are captured by coated antibodies avoiding diffusion in supernatant, protease degradation or binding on soluble membrane receptors. After cell removal, the captured cytokines are revealed by tracer antibodies and appropriate conjugates. The dual colour Elispot allows you to monitor the production of two cytokines simultaneously in the same well.
Recognizes natural human Interferon gamma and Perforin
|Components||5 x 96 tests||10 x 96 tests||15 x 96 tests||20 x 96 tests|
|10 x concentrate buffer for the preparation of AEC buffer||1 x 5ml||2 x 5ml||3 x 5ml||4 x 5ml|
|50 x concentrate AEC substrate buffer||1 x 1ml||2 x 1ml||3 x 1ml||4 x 1ml|
|Anti-FITC antibody HRP conjugate||1 x 100µl||2 x 100µl||3 x 100µl||4 x 100µl|
|Bovine Serum Albumin||1 x 1g||2 x 1g||3 x 1g||4 x 1g|
|Human IFN? Capture antibody||1 x 500µl||2 x 500µl||3 x 500µl||4 x 500µl|
|Human Perforin Capture Antibody||1 x 500µl||2 x 500µl||3 x 500µl||4 x 500µl|
|IFNγ FITC conjugated detection antibody||1 vial||2 vials||3 vials||4 vials|
|Perforin Biotinylated Detection Antibody||1 vial||2 vials||3 vials||4 vials|
|Ready-to-use BCIP/NBT substrate buffer||1 x 50ml||2 x 50ml||3 x 50ml||4 x 50ml|
|Streptavidin - Alkaline Phosphatase conjugated||1 x 50µl||2 x 50µl||3 x 50µl||4 x 50µl|
ab59703 has not yet been referenced specifically in any publications.