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This question is more challenging than the previous one, because shifting the cutoff date to an earlier date potentially changes both the tenure and stop flag for customers. Figure 6-17 illustrates what happens. Customers who are now stopped, such as customers 3, 6, and 7, are active as of the earlier cutoff date.

and JPL have jointly investigated the applicability of the BPT-4000 to NASA deep-space missions [43] where throttle range and efficiency are important. The throttleability of the BPT-4000 engine [44] from power levels 1 kW to 4.5 kW was demonstrated with very high efficiency observed at low power levels for this size thruster. Hall thruster technology will continue to be developed and used in commercial and scientific missions due to their high performance and relatively simple construction and operation.

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to manually edit the file. Dreamweaver picks up and shows all the objects inside a category s folder, so you don t need to manually add new objects to the insertbar.xml file. You re not limited to the default categories on the Insert bar. If you want to add another category, simply add a new subfolder and the necessary entries to the insertbar.xml file (which I cover next). For example, I ve developed a number of custom objects for inserting sound and digital video files, and I wanted to group them on a new category of the Insert bar. In my file-management program, I created a folder called Media within the Dreamweaver MX 2004\Configuration\Objects folder and moved all my special object files into this new folder. After editing the insertbar.xml file and restarting Dreamweaver, Media appears on the Insert bar in the order in which I placed the entry in insertbar.xml.

Challenge: Create a mind for the computer opponent that will give the user a fun and variable experience.

Each of the disjuncts in this expression is a conjunctive predicate. In this chapter we study methods to detect global predicates that are conjunctions of local predicates. We will implement the interface which abstracts the functionality of a global predicate evaluation algorithm. This interface is shown below:

EnumeratedType ::= NotationType ::=

If you feel most comfortable with creating styles in Dreamweaver, you can make all your changes through the same CSS Style Definition dialog box. Simply choose the style you want to alter in the CSS Styles panel and click the Edit Style button at the bottom of the panel to the left of the Trashcan. The CSS Style Definition dialog box reopens, ready to be modified. Click Apply to see your changes immediately in the Design view and click OK when you re finished.

3.8 The IOGEAR Bluetooth printer adapter comes with a Bluetooth dongle for your computer, in case you don t have built-in Bluetooth.

The rst stage in a comprehensive PTM analysis of a protein of interest is puri cation. Depending on the initial level of puri cation, this can be most conveniently achieved by gel electrophoresis, either a 1D or a 2D gel. Often electrophoresis may give clues to the nature of modi cation; for example, phosphorylation of a protein can result in spots separated horizontally on a 2D gel due to differential pI values between phosphorylated and nonphosphorylated states of the protein of interest. A useful rst stage in the process is to accurately identify the molecular ion; comparisons between the expected and measured mass can give initial information about which modi cations may be present. After gaining information on the intact protein, detailed information regarding site(s) of modi cation may be obtained by analysing peptides obtained after enzymatic or chemical degradation. A typical combination would be to use trypsin in one experiment and then to use endoproteinase Asp-N or Glu-C in a second experiment. Modi ed oligo-/polypeptides in digests can be identi ed by unexpected molecular ions and then analysed by product ion scanning to determine the amino-acid residues at which PTMs have taken place. Acetylation (often on arginine amino-acid residues) is easiest to identify. Phosphorylation can be either stable or labile (phosphotyrosine tends to be stable, phosphothreonine less so, whilst phosphoserine tends to be labile), but can usually be seen. Unfortunately, sulphation and glycosylation modi cation sites can be much more labile and less easy to identify by tandem mass spectrometry.

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