spacer gif spacer gif spacer gif spacer gif spacer gif
 QUICK SEARCH:   [advanced]


spacer gif
     Home     Help     Feedback     Subscriptions     Archive     Search     Table of Contents    


Right arrow Help viewing high resolution images
Right arrow Return to article
(Downloading may take up to 30 seconds.
If the slide opens in your browser, select File -> Save As to save it.)

Click on image to view larger version.


Figure 5


Fig. 5. Both CG10806 and CG31052 localise to the apical plasma membrane. Flies transgenic for UAS-CG10806::eYFP or UAS-CG31052::eYFP fusions were crossed to GAL4 line c42 to drive expression in the Malpighian tubule principal cells, and subcellular localisation in 1-week-old adult progeny was established by confocal microscopy. DAPI was used to visualise the nuclei (blue) to demonstrate the apical localisation of the transgenic proteins. (A) CG10806 transcript A; (B) CG10806 transcript B; (C) CG31052. (D,E) For comparison, a vha55::GFP transgene marking the apical membrane (D) and immunocytochemistry against the Na+-K+ ATPase {alpha} subunit (a marker of the basolateral membrane), together with GFP-tagged vhaSFD to mark the apical membrane (E) are also shown. Lu, apical tubule lumen; AM, apical plasma membrane; BM, basal plasma membrane. Scale bars: 10 µm.





Right arrow Return to article