immunofluorescence microscopy
Sign in to savethumb|278x278px|Vasculature of porcine skin under fluorescence ([[Smooth muscle actin with AlexaFluor 488). Green = smooth muscle actin (SMA) with Alexa 488 fluorophore. Blue = DAPI counterstain. Red = auto-fluorescence. ]]
Article
10 sectionsContents
- Types
- Preparation of fluorescence
- Primary (direct)
- Secondary (indirect)
- Limitations
- Advances
- Notable people
- See also
- References
- External links
thumb|278x278px|Vasculature of porcine skin under fluorescence ([[Smooth muscle actin with AlexaFluor 488). Green = smooth muscle actin (SMA) with Alexa 488 fluorophore. Blue = DAPI counterstain. Red = auto-fluorescence. ]]
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.