Micropatterned coverslips were fixed with 4% paraformaldehyde (Electron Microscopy Sciences 15713) in warm medium for 30 min, rinsed three times with PBS−/−, and blocked and permeabilized for 30 min with 3% normal donkey serum (Jackson ImmunoResearch 017-000-121) and 0.5% Triton X-100 (Sigma-Aldrich 93443) in PBS−/−. Specimens were incubated with primary antibodies for 1.5 hr at room temperature, washed three times for 5 min each in PBS−/−, incubated with secondary antibodies conjugated with Alexa 488, Alexa 555, Alexa 594, or Alexa 647 (Molecular Probes) at 1/1000 dilution for 1 hr at room temperature. After 30 min incubation with 100 ng/ml 4′,6-diamidino-2-phenylindole (DAPI; Thermo Fisher Scientific D1306), specimens were washed three times with PBS−/−. Coverslips were mounted on slides using ProLong Gold antifade mounting medium (Molecular Probes P36934).
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How to cite:
Readers should cite both the Bio-protocol preprint and the original research article where this protocol was used:
M Piccolo, F and Brivanlou, A(2022). Immunofluorescence. Bio-protocol Preprint. bio-protocol.org/prep1887.
Beaudoin, A. J., Brivanlou, A. H., Carroll, T. S., Kastan, N. R., Laundos, T. L., Piccolo, F. M., Santis, R. D., Etoc, F., Gnedeva, K., Haremaki, T., Hudspeth, A., Luo, J. and Tian, Q. Role of YAP in early ectodermal specification and a Huntington's Disease model of human neurulation. eLife. DOI: 10.7554/eLife.73075
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