Category:Team PSU 4

Results: “In contrast, anti-NXR was very specifically observed at the tubule-like structures in the anammoxosome (Fig. 8) in both transverse (Fig. 8C) and longitudinal (Fig. 8A, B, and D) sectioned tubules.”

Fig 7 - “K. stuttgartiensis cells incubated with affinity-purified antibodies against HZS. Thin sections were incubated with 1:200-diluted anti-HZS (A to C) or 1:300-diluted anti-HZS (D). Gold particles were visible only inside the anammoxosome. “

Fig 4 - “K. stuttgartiensis cells incubated with antibodies against kustc0457/58. Thin sections were incubated with 1:150-diluted anti-kustc0457/58 (A and B), 1:50-diluted preimmune serum (C), or 1:100-diluted anti-kustc0457/58 (D). Gold particles were visible only inside the anammoxosome, preferentially located toward the inner side of the anammoxosome membrane. Incubation with preimmune serum led to the detection of a few gold particles throughout the cell.”

Results: “anti-NXR was very specifically observed at the tubule-like structures in the anammoxosome (Fig. 8) in both transverse (Fig. 8C) and longitudinal (Fig. 8A, B, and D) sectioned tubules.”

Fig 7 -“K. stuttgartiensis cells incubated with affinity-purified antibodies against HZS. Thin sections were incubated with 1:200-diluted anti-HZS (A to C) or 1:300-diluted anti-HZS (D). Gold particles were visible only inside the anammoxosome. “

Fig 5- “ Thin sections were incubated with 1:300-diluted anti-HOX (A and B) or 1:100-diluted anti-HOX (C and D). Gold particles were visible only inside the anammoxosome. HOX appeared to be preferentially localized in the proximity of the anammoxosome membrane.”

Fig 4 - "K. stuttgartiensis cells incubated with antibodies against kustc0457/58. Thin sections were incubated with 1:150-diluted anti-kustc0457/58 (A and B), 1:50-diluted preimmune serum (C), or 1:100-diluted anti-kustc0457/58 (D). Gold particles were visible only inside the anammoxosome, preferentially located toward the inner side of the anammoxosome membrane. Incubation with preimmune serum led to the detection of a few gold particles throughout the cell.”

Fig 7- “K. stuttgartiensis cells incubated with antibodies against HZS. Thin sections were incubated with 1:100-diluted anti-HZS (A and B), 1:50-diluted preimmune serum (C), or 1:100-diluted anti-HZS (D). Gold particles were visible only inside the anammoxosome.”

Fig. 6 stuttgartiensis cells incubated with antibodies against HDH. Thin sections were incubated with 1:100-diluted anti-HDH (A and B), 1:50-diluted preimmune serum (C), or 1:100-diluted anti-HDH (D). Gold particles were visible only inside the anammoxosome"

Results: “In contrast, anti-NXR was very specifically observed at the tubule-like structures in the anammoxosome (Fig. 8) in both transverse (Fig. 8C) and longitudinal (Fig. 8A, B, and D) sectioned tubules.”

Figure 1B shows the localization of TonB in the E. coli cell envelope via fluorescence microscopy.

Figure 1A shows FepA localizing at the E. coli cell envelope via fluorescence microscopy.

Figure 5 shows localization of RseA fragments in the inner membrane of E. coli via Western Blot analysis.

Figure 4A shows the localization of IcsA at the polar caps, shown by the arrows, in a wild-type strain of S. flexneri. This was detected by indirect immunofluorescence using an antibody to IcsA.

Figure 3b (middle image) shows localization of SepF at the cell septum using fluorescence microscopy.

Figure 2 shows localization of Su48 at the centrosome. Fluorescence microscopy was used to visualize Su48 inside the cell.

In Figure 6B, DprA is shown to facilitate the annealing of DNA in the present of single-stranded binding proteins via gel electrophoresis. Both double-stranded and single-stranded DNA are present when DprA is present. Only single-stranded DNA is present in the absence of DprA.

In Figure 1B, wild-type cells of E. coli were fixed and the FtsN protein was visualized via immunofluorescence microscopy. FtsN is shown to be localized at the septum, indicated by the arrows.

Figure 5A shows a flagged YciB being expressed in Bacillus subtilis and analyzed via immunofluorescence. The arrows within the figure are locating areas with a main concentration of Ycib-FLAG. These locations are near areas of division and cell poles.