Cell Signaling Technology

Immunofluorescence Protocol without Permeabilization

IMPORTANT: Please refer to the APPLICATIONS section on the front page of the datasheet to determine if this product is validated and approved for use on cultured cell lines (IF-IC) or frozen tissue sections (IF-F).

A. Solutions and Reagents

NOTE: Prepare solutions with Milli-Q or equivalently purified water.

B. Specimen Preparation

I. Cultured Cell Lines (IF-IC)

NOTE: Cells should be grown, treated, fixed and stained directly in multi-well plates, chamber slides or on coverslips.

  1. Aspirate liquid, then cover cells to a depth of 2–3 mm with 4% formaldehyde in PBS.
    NOTE: Formaldehyde is toxic, use only in fume hood.
  2. Allow cells to fix for 15 minutes at room temperature.
  3. Aspirate fixative, rinse three times in PBS for 5 minutes each.
  4. Proceed with Immunostaining (Section C).

II. Frozen/Cryostat Sections (IF-F)

  1. For fixed frozen tissue proceed with Immunostaining (Section C).
  2. For fresh, unfixed frozen tissue, please fix immediately, as follows:
    1. Cover sections with 2–4% formaldehyde in PBS.
      NOTE: Formaldehyde is toxic, use only in fume hood.
    2. Allow sections to fix for 15 minutes at room temperature.
    3. Rinse slides three times in PBS for 5 minutes each.
    4. Proceed with Immunostaining (Section C).

C. Immunostaining

NOTE: All subsequent incubations should be carried out at room temperature unless otherwise noted in a humid light-tight box or covered dish/plate to prevent drying and fluorochrome fading.

  1. Block specimen in Blocking Buffer for 60 minutes.
  2. While blocking, prepare primary antibody by diluting as indicated on datasheet in Antibody Dilution Buffer.
  3. Aspirate blocking solution, apply diluted primary antibody.
  4. Incubate overnight at 4°C.
  5. Rinse three times in PBS for 5 minutes each.
    NOTE: If using primary antibodies directly conjugated with Alexa Fluor® fluorochromes, skip to step C8.
  6. Incubate specimen in fluorochrome-conjugated secondary antibody* diluted in Antibody Dilution Buffer for 1–2 hours at room temperature in dark.
  7. Rinse in PBS as in step 5.
  8. Coverslip slides with Prolong® Gold Antifade Reagent.
  9. For best results, examine specimens immediately using appropriate excitation wavelength. For long-term storage, store slides flat at 4°C protected from light.

*Recommended Secondary Antibodies:

Anti-Rabbit

Anti-Mouse

Anti-Rat

posted December 2010

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