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Table 3-2: Summary of PivotTable Tools Tab Groups TAB GROUP PivotTable PURPOSE Accessing the PivotTable Options dialog box, changing the PivotTable report name, showing Report Filter pages, and toggling the Generate Get PivotTable option. Access the Field Settings dialog boxes, expand and collapse fields in the Row Labels or Column Labels area. Group and ungroup items in the Row Labels or Column Labels areas of the PivotTable. Sort data and items in the PivotTable. Refresh the PivotTable report, change the data source, and access the Connection Properties dialog box. Clearing filters, removing all fields from the PivotTable report, selecting PivotTable areas, and moving the PivotTable report. Create PivotCharts, manage Calculated Fields and Calculated Items, and access OLAP tools. Toggle the display of the PivotTable Field List dialog box, report expansion indicators, and field headers.

The vast majority of Dreamweaver s settings are controlled through the Preferences dialog box. You can open Preferences by choosing Edit Preferences (Dreamweaver Preferences) or by using the keyboard shortcut Ctrl+U (Command+U). Within Preferences, you find 20 different subjects listed on the left side of the screen. As you switch from one category to another by selecting a name from the Category list, the options available for that category appear in the main area of the dialog box. Most changes to Preferences take effect immediately after you close the window by clicking the OK button. This chapter covers all the options available in each category; the categories are grouped by function rather than by order of appearance in the Category list.

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If a printer has options for printer s marks, they display in the Type popup menu, but most simply have one option: Default. You can also adjust the thickness of the printer s marks using the Weight popup menu settings of 0.125, 0.25, and 0.5 points; the default is 0.25 points (a hairline rule). You can also control the offset of crop marks from the page corners by adjusting the Offset value; the default of 0.833 inches (6 points) usually suffices. For all of these, check with your service bureau. Because printer s marks print outside the page, your paper size may not be large enough to print the printer s marks. For example, if your page is 81 2 11 inches and your paper is the same size, no room is available for the printer s marks. (The page preview subpane on the left of the Print dialog box shows you whether printer s marks fall outside the page s boundaries.) Be sure that your paper size is at least 1 inch wider and taller than your page size if you use printer s marks.

The keys listed assume that you re not using the Transition Navigation Keys, which are designed to emulate Lotus 1-2-3. You can select the Transition Navigation Keys option in the Advanced tab of the Excel Options dialog box. This option is in the Lotus Compatibility section.

Listing 6-10: ch06_gmaps_geotags.js (Part 4 of 8)

uorescent protein variants (known as BFP, CFP and YFP respectively). A further alternative to GFP is DsRed, which is naturally found in the coral Discosoma. Wild-type DsRed is an obligate tetramer but mutant DsRed proteins that are monomeric can now be used in place of GFP in fusion proteins. Biological and chemical approaches can be combined to yield similar possibilities to the fusion protein approach described above. A tetracysteine motif (CCXXCC; where X is a noncysteine amino-acid residue) can be engineered into any protein of interest at any required position, in principle (see 3). This motif is highly selective for binding to biarsenical uorophores based upon uorescein. Biarsenical uorophores are able to permeate cells and remain non- uorescent until chelated by the tetracysteine motif (Figure 4.25). Biarsenical uorophores are particularly partial to being across a -helix with the molecular plane oriented perpendicular to the direction of the helix. Hence, using such uorophores, an engineered protein of interest can be expressed in cells in situ then tagged in situ by any one of a whole range of biarsenical dyes with slightly different structures that are able to uoresce at different wavelengths. A nal biological approach to extrinsic labelling that is worth noting for the interested chemical biology reader is the use of cyanine (Cy) dyes (in particular Cy3 and Cy5). At rst sight these look complex, but they can be introduced into DNA by a method known as nick

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