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You can also use the TouchUp Object tool to move or nudge objects. Click on a single object or marquee a group of objects on a page, and then click and drag the selection to a new location. You are limited to moving objects on a single page. You can t select an object on one page and drag it to another PDF page. For moving objects to different pages you need to cut the selection, move to another page, and choose Edit Paste. If you want to nudge objects, create a selection with the TouchUp Object tool and press the arrow keys on your keyboard to move the object right, left, up, or down.

while at 1 mm F 5 1018 quanta/s (quanta per second). For a thermal detector, the change in temperature is linearly proportional to the power deposited. Assuming uniform spectral absorption, a thermal detector produces the same response for 1 W at 500 nm as for 1 W at 1 mm. Thermal detector arrays are commonly used in infrared spectral ranges where semiconductor detectors are expensive and dif cult to fabricate and where relatively broad and uniform spectral response is desirable. Noise characteristics of thermal detectors are not generally as attractive as photon detectors, however, so most high-performance systems use photon detectors. Responsivity, de ned as R output signal input power (5:25)

Although it s quite easy to play QuickTime and AVI windows from within Director, it s helpful to learn a few Lingo commands to control navigation and start and stop QuickTime movies. Director provides a simple interface to get you started creating Lingo scripts. The following section shows you how to create a simple navigational script by using Director s Behavior Inspector. After you learn how to use the Behavior Inspector, you can create scripts that control QuickTime and AVI movies.

reported that the SP6 tail gene is anked by an upstream region that contains a promoter and a downstream region that contains a putative Rho-independent transcription terminator, giving it a cassette or modular structure almost identical to the structure of the tail genes of coliphages K1E, K5, and K1-5 (Scholl et al 2002) It was concluded that phages SP6, K1-5, K5, and K1E are very closely related but have different tail ber proteins, which allows each phage to have different host speci cities (Scholl et al 2002) The observation of a similar tail genome motif in both the Salmonella phage SP6 and the coliphages K1E, K5, and K1-5 indicates that this genomic construct might serve in the development of a modular phage platform that could operate over a wide bacterial host range The presence of such host range platforms is described more fully below.

click on me Fast Fourier Transform hot button ~ at the top of the PROBE window. From the resulting plot, shown in Fig. 15.31c, we confirm that the signal amplitude is 1000 times larger than the noise components. It should be mentioned that the FFT in Fig. 15.31c is the result of a 5-ms transient simulation (i.e., 50 cycles at 10 kHz). In general, the more cycles in the transient analysis, the better is the frequency resolution of the FFT. Op-amps from the ANALOG library with gains of 10 6 and supply rails of 15 V were used in the simulation .

= 4.86

Other mechanisms have been found that permit the expansion of the bacterial host range of phage based on the use of more than one bacterial receptor One such mechanism is site-speci c recombination systems that permit phage to switch between alternative tail ber proteins Recombination sites for DNA invertases and recombination sitelike sequences have been observed to ank gene segments conferring the speci city of a given phage for its host receptors When combined with the properties of DNA inversion, it is possible that the site-speci c recombination enzymes could be responsible for the exchange of host range determinants Sandmeier (1994) extensively reviewed the scienti c literature in this area, providing insight into the putative role of DNA inversion enzymes in the recombination of tail ber gene segments between genomes.