ICC/IF

Immunocytochemistry (ICC) and Immunofluorescence (IF) are powerful techniques used to detect and visualize specific proteins or antigens within cells or tissues. ICC focuses on identifying the localization of a target protein within cells by using a primary antibody that binds to the protein. The signal is then visualized through a secondary antibody conjugated to a fluorophore, allowing researchers to observe antigen expression and its subcellular localization under a fluorescence microscope. Similarly, IF is a light microscopy-based method that detects biomolecules at a quantitative level, using antibodies to bind specific epitopes on antigens. The high binding specificity of antibodies enables the precise detection of target molecules. AREX offers a wide range of high-quality antibodies optimized for both ICC and IF, ensuring reliable and reproducible results in research applications

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 ICC(Immunocytochemistry)

Immunocytochemistry (ICC) is a common laboratory technique that is used to anatomically visualize the localization of a specific protein or antigen in cells by use of a specific primary antibody that binds to it. The primary antibody allows visualization of the protein under a fluorescence microscope when it is bound by a secondary antibody that has a conjugated fluorophore. ICC allows researchers to evaluate whether or not cells in a particular sample express the antigen in question. In cases where an immunopositive signal is found, ICC also allows researchers to determine which sub-cellular compartments are expressing the antigen.

IF(Immunofluorescence)

Immunofluorescence (IF) is a light microscopy-based technique that allows detection and localization of a wide variety of target biomolecules within a cell or tissue at a quantitative level. The technique utilizes the binding specificity of antibodies and antigens. The specific region an antibody recognizes on an antigen is called an epitope. Several antibodies can recognize the same epitope but differ in their binding affinity. The antibody with the higher affinity for a specific epitope will surpass antibodies with a lower affinity for the same epitope.

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