For anti-phospho-Stat antibody staining, female flies were dissected in dissection medium containing 1× phosphatase inhibitors (PhosSTOP, Sigma-Aldrich), and fixed (4% paraformaldehyde, 1X PBS and 1× phosphatase inhibitors) for 2 hours at 4℃. Finally, samples were washed once with 0.5% PBT then washed again with 0.3% PBT before primary antibody treatment. The anit-phospho-Stat antibodies (1:400) were prepared in 0.3% PBT and incubated with samples overnight at 4℃. The following secondary antibodies, conjugated with fluorescent dye were used at 1:400 dilutions: Alexa-488, Alex-568 or Alexa-647 (Invitrogen, Molecular Probes).
Readers should cite both the Bio-protocol preprint and the original research article where this protocol was used:
Wu, J, Chang, Y and Jang, A(2024). Quantitative assessment of Stat92E-GFP expression and anti–p-Stat staining during oogenesis. Bio-protocol Preprint. bio-protocol.org/prep2626.
Wu, J., Wang, C., Chen, R., Hung, L., Tsai, Y., Chan, Y., Chang, Y. and Jang, A. C.(2022). Spatiotemporal gating of Stat nuclear influx by Drosophila Npas4 in collective cell migration. Science Advances 8(29). DOI: 10.1126/sciadv.abm2411
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