Immunofluorescent tissue (cell) chemical staining method - Direct method, a fluorescent antibody staining method.
Principle
An antibody labeled with fluorescein of known specificity binds directly to the corresponding antigen in the tissue cells, and specific fluorescence is seen under a fluorescence microscope at the site where the antigen is present.
Appliance
It is suitable for the detection of protein antigens with high concentration, such as the examination of kidney and skin antigens. Also commonly used in clinical practice for the detection of bacteria, spirochetes, protozoa and fungi.
Operation method
Check antigen method; check antibody method
Materials and Instruments
[Materials] Specific antigen; specific antibody;
Move
1. Staining After fixation, the sections were stained with fluorescent antibody diluted to the staining potency for 30 minutes at room temperature or 37~C in a wet box.Wash the sections to remove the fluorescent antibody, immerse the sections in PBS at pH 7.2-7.4 and wash with shaking or vibration for 5 minutes each time, then wash with distilled water for 1 minute to remove salt crystals.3. Sealing and observation The sections were sealed with 50% glycerol buffer (0.5 mol/L phosphate buffer, pH 9.0-9.5) or anti-quenching agent, and then placed under a fluorescence microscope for observation.
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Da — when not otherwise indicated, molecular weight units are daltons. Mw — weight-average molecular weight. Mn — number-average molecular weight.
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Cite this article
Aladdin Scientific. "Immunofluorescence histochemical direct method" Aladdin Knowledge Base, updated 9 juin 2025. https://www.aladdinsci.com/eu_fr/faqs/immunofluorescence-histochemical-direct-en.html
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