Replication Data for:CELL-REPORTS-D-23-04977R2

Published: 18 March 2024| Version 1 | DOI: 10.17632/7jj9zs9rrj.1
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Figure 2A: BALB/c mice were transurethrally infected with WT, Δndk, or Δndk+ for 6 h p.i. The bladder tissues were analyzed for the amount of UpIII by western blotting Figure 3A:Western blot analysis of the NDK protein levels in the culture supernatant and pellet of WT, Δndk, or Δndk+ that was cultured in logarithmic phase (OD600=0.6), and a periplasm protein DnaK was used as a loading control to eliminate the possibility that the presence of NDK in culture supernatant is from dead bacteria. Figure 3C:5637 cells were infected with WT, Δndk, or Δndk+ for 4 h p.i. The cell lysates were analyzed for the amount of cleaved Caspase-1 p10 and pro-Caspase-1 by western blotting. Figure 3D:The amount of full-length GSDMD and N-GSDMD in 5637 cells infected with WT, Δndk, or Δndk+, respectively, at 4 h p.i. Figure 3E:The amount of full-length GSDMD and N-GSDMD in mouse bladders infected with WT, Δndk, or Δndk+, respectively, at 6 h p.i. Figure 3F:Western blot analysis of the NDK protein levels in CFT073 infected 5637 cells supernatant and pellet.

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