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DyLight Protocols for IF

Immunofluorescence microscopy is used to localize specific constituents in tissue sections or immobilized cells using fluorescent tags as labels. The antibody/antigen complex is labelled with any of a variety of fluorochromes emitting light from the near UV to the near IR. Usually FITC, a fluorescein derivative, is used for routine work and shows a yellow/green color. Red is often visualized using Texas Red, rhodamine or Cy3. Blue occurs when AMCA or Cascade Blue is used.

Dylight fluorochromes are the finest ones bringing several advantages:


Fluorescent microscopes contain limit filters that are optimized for each fluorochrome. Confirm that your microscope is optimized for each dye you plan to use in your experiment. Black and white or color photography or enhanced imaging are often used to record data.

Reagents Required

Fluorescein Secondary Antibody. Prepare dilution of fluorescein conjugated secondary antibody (1:200) in Antibody Dilution Buffer. Use secondary antibody conjugate against the same species as the primary antibody.
Dylight Secondary antibody. Prepare dilution of Dylight conjugated secondary antibody (1:5000) in Antibody Dilution Buffer. Use secondary antibody conjugate against the same species as the primary antibody.
Bis-Benzimide Solution. Prepare reagent at 0.5 mg/ml in PBS buffer.
Aqueous Mounting Media. AQUA-POLY/MOUNT

Procedure

  1. Grow cells on sterile 12 mm glass coverslips placed in 24 well culture plates. Remove culture medium.
  2. Gently wash cells 3 times with ice cold PBS for 5 minutes per wash.
  3. Fix cells by adding a volume of 1% formaldehyde in PBS equal to the original volume of culture medium. Incubate on ice for 5 minutes. Remove the fixative and wash as in Step 2.
  4. Permeabilize cells for 20 minutes on ice with Permeabilization buffer.
  5. Prepare primary antibody appropriately diluted in Antibody Dilution Buffer. React cells with primary antibody for 1 h at room temperature.
  6. Wash as in Step 2.
  7. Prepare dilution of fluorescent conjugated affinity purified secondary antibody. React cells for 1 h at room temperature with reagent. Alternatively, use a biotin conjugated secondary antibody followed by a wash as in Step 2. Add fluorescein conjugated streptavidin (code# 039S000-02) diluted 1:200 in PBS buffer. React for 30 minutes at room temperature.
  8. Wash as in Step 2.
  9. Counterstain cells with bis-benzimide solution for 15 minutes at room temperature.
  10. Wash as in Step 2.
  11. Add aqueous mounting agent. Affix coverslips to slides. Allow coverslips to dry in the dark before viewing.


References
1. Ascoli and Maul. 1991. J. Cell Biol. 112:785-795.
2. Antibody Techniques. V.S. Malik and E.P. Lillehoj, eds. Academic Press, 1994.