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Immunofluorescence (IF) is a common morphological approach used to determine the distribution of subcellular components. Antibodies that conjugated with fluorescent dyes are required in IF assay. The antibody specifically recognizes the antigen by binding to the epitope of target, and the fluorophore will be detected under a fluorescent microscope. \n

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if protocol cultured cell

IF protocol-Cultured Cell

Note: This method is suitable for immunofluorescence on tissue sample.

Reagents:

PBS: To prepare 1 L 1X PBS: dissolve 8g of NaCl, 0.2g of KCl, 1.44g of Na2HPO4, 0.24g

of KH2PO4 in 800ml distilled H2O, then adjust pH to 7.4 with HCl and adjust volume

to 1L with additional distilled H2O.

Permeablization solution: 0.3% Triton X-100 in PBS. To prepare 100 mL: add 300 µl

Triton X-100 to 100 mL PBS and mix. (Optional)

Blocking buffer: To prepare 10 ml, add 0.5 ml normal serum in PBS and mix well.

While stirring, add 30 µl Triton™ X-100.

NOTE: Select serum that are from the same species as the secondary antibody.

Antibody dilution buffer: To prepare 10 ml, add 30 µl Triton X-100 to 10 ml 1X PBS.

Mix well then add 0.1g BSA.

Antifade Reagent

Equipment:

Adhesive slides

PAP pen

https://www.creative-diagnostics.com/immunofluorescence-protocol-stick-section.h

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