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 3


Fig. 3. PLCβ1a and PtdIns(4,5)P2. (A) HeLa cells were stimulated with histamine (100 µM, arrow) after overnight incubation with 1 µM PMA. The red trace depicts the mean normalized fluorescence intensity of GFP-PLCβ1a; the black trace depicts the mean normalized fluorescence intensity of the Fura Red dye in a region of interest in the cytosol (n=7; the error bars depict standard error). The Fura Red dye was excited at 488 nm and detected with a long-pass 650-nm filter. Therefore, an increase in intracellular Ca2+ correlates with a decrease in fluorescence intensity. For the exact settings used, see Materials and Methods. (B) HeLa cells expressing RFP-PH{delta}1. Scale bar: 10 µm. (C) HeLa cells coexpressing PLCβ1a (red trace), PH{delta}1 (black trace) and bradykinin type 2 receptor (B2R) were first stimulated with histamine (100 µM; at t=15 seconds, first arrow) and then with bradykinin (1 µM; at t=115 seconds, second arrow).





Right arrow Return to article