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|Sample type||Average %||Range|
|Cell culture supernatant||95||% - %|
|Serum||100||% - %|
Abcam’s Human High Sensitivity IL-2 ELISA is to be used for the in-vitro quantitative determination interleukin-2 (IL-2) in Human sera, plasmas, buffered solutions or cell culture media.
A monoclonal antibody specific for IL-2 has been coated onto the wells of the microtiter strips provided. Samples, including standards of known IL-2 concentrations, control specimens or unknowns are pipetted into these wells. During the first incubation, the standards or samples and a biotinylated monoclonal antibody specific for IL-2 are simultaneously incubated. After washing, the enzyme Streptavidin-HRP, that binds the biotinylated antibody is added, incubated and washed. A TMB substrate solution is added which acts on the bound enzyme to induce a colored reaction product. The intensity of this colored product is directly proportional to the concentration of IL-2 present in the samples.
This kit will recognize both endogenous and recombinant Human IL-2.
Get results in 90 minutes with Human IL-2 ELISA Kit (ab174444) from our SimpleStep ELISA® range.
|Components||Identifier||1 x 96 tests|
|10X Standard Diluent Buffer||Black||1 x 25ml|
|200X Wash Buffer||White||1 x 10ml|
|Amplification Diluent||Brown & blue spot||1 x 25ml|
|Amplifier||Yellow||1 x 200µl|
|Biotinylated anti IL-2||Red||1 x 400µl|
|Biotinylated Antibody Diluent||Red||1 x 7.5ml|
|Chromogen TMB Substrate Solution||1 x 11ml|
|HRP Diluent||Red||1 x 25ml|
|IL-2 Microplate (12 x 8 well strips)||1 unit|
|IL-2 Standard (Lyophilized)||Yellow||2 vials|
|Standard Diluent (Human Serum)||1 x 7ml|
|Stop Reagent||Black||1 x 11ml|
|Streptavidin-HRP||2 x 5µl|
Our Abpromise guarantee covers the use of ab46054 in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
|Sandwich ELISA||Use at an assay dependent concentration.|
Representative standard curve using ab46054
ab46054 has not yet been referenced specifically in any publications.