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PivotTables are powerful tools and with that power comes some unavoidable complexity. This section covers the more common problems that users encounter when creating and using PivotTables and suggests solutions.

(7.9)

Caution You won t be able to use this behavior until you name your frames as detailed in the section Naming your frames, earlier in this chapter

Figure 6-18: Layout parts as they look in Layout mode (top) and in Preview mode or when printed (bottom).

sub delroute { my ($routeid) = @_; $dbh->do(sprintf( delete from ch13_routesimple where routeid=%s , $routeid)); $dbh->do(sprintf( delete from ch13_routepoints where routeid=%s , $routeid)); xmlmessage( Route deleted ); }

5.9 For people who seriously need help getting organized, OmniFocus is a good option it s something of an investment up front, but it can save you lots of time in the long run.

The Save As dialog box opens, where you choose the disk and folder to store the exported Web page, as well as the page s file name. After you click Save, the XHTML Export Options dialog box opens, in which you specify how InDesign converts the layout to the Web format. The following sections describe the options in that dialog box s three panes, although you want to be sure to consult with your Webmaster on preferred settings if you re new to working on a specific Web site s pages.

For an easy way to draw free-form shapes, use the Pencil tool. It simply traces the movement of your mouse (or pen tablet) as you move it, in much the same way as a pencil works on paper. Although not as exact as the Pen tool, the Pencil tool does create B zier curves that you can later edit.

VxB=p, J + E - ,

have needed to be developed. These include the following: liquid liquid diffusion, vapour diffusion and dialysis. The liquid liquid diffusion method (Figure 6.8) uses a narrow bore glass capillary to place a layer of precipitant (approximately 5 l) in contact with a layer of biological macromolecule solution (approximately 5 l) over a small surface area. The two layers are intended to gradually diffuse together to bring about crystallisation. There are two alternative vapour diffusion methods, namely the hanging drop method (Figure 6.9) and the sitting drop method (Figure 6.10). The former method relies upon surface-tension effects to position a combined aliquot of biological macromolecule solution and precipitant (approximately 10 l) on a glass slide, inverted over a well containing precipitant solution (approximately 1 ml), all in a sealed box. The latter method is an alternative method used if surface-tension effects are insuf cient to sustain a hanging drop during the crystallisation process. In both cases, the separated solutions are expected to diffuse together by slow vapour diffusion to bring about crystallisation. Finally, the dialysis method (Figure 6.11) separates biological macromolecule solution from precipitant by means of a semipermeable membrane, through which precipitant will diffuse to initiate crystallisation. This technique is quite versatile in that the precipitant may be altered at will and crystallisations may be performed on a range of different scales. Once crystals have been obtained, they must be isolated and prepared for X-ray crystal diffraction studies. This too is problematic, since biological macromolecule crystals are not the dense packed structures familiar to chemists used to working with small molecules. Rather,

Figure 14.15. Best-effort data spectral ef ciency. 10-MHz case (10-MHz DL + 10-MHz UL)

(6.5-4)

Click the View Keywords for Selection button on the toolbar to display the Keywords dialog box. Click the Auto-Apply button at the top to display the Auto-Apply pane (see figure 8.12). This pane contains the same list of keywords as the Inspector tab it just gives you a different way to apply them.

If you want to use the last saved version of the document (and disregard the recovered data), close the file (choose File Close or press +W or Ctrl+W) without saving and then open the file (choose File Open or press +O or Ctrl+O).