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This way, if you find that you have misconfigured Postfix, and you can t figure out what you did wrong, you can simply delete your configuration file and start over from scratch with the default. Next, use your favorite text editor to open the main.cf file; for the example, I use gedit (shown in Figure 22-2), launched with the command gedit main.cf. (Using a text command to launch gedit in this case allows the file to be open with superuser privileges. If you launch gedit from the main menu, you do so with your regular user privileges.)

6

Using text mode . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 211 Using graphical tools . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 213

Figure 3.63. Schematic of SPR protein binding experiment. The sensor is equilibrated with buffer before addition of a protein solution. This changes n s immediately above the sensor surface giving a sharp decrease in re ectivity. Protein binding is followed as a change in SPR angle ( ) over time. When the surface becomes saturated, the SPR angle reaches a maximum. Loosely bound protein is removed by washing with buffer. Extent of adsorption is given by the difference between initial and nal SPR angles while the rate of binding may be measured from the steepest part of the positive slope.

The site is subject to claims by indigenous owners, leading to disputes, delays and compensation payments The site is subject to heritage or preservation conditions that impose additional Public sector/ contractor design and construction costs

Characteristics of a typical light alternator Viewing Capability Viewing Average luminance surface per panel Ft-L height x width (in2 ) Viewing height (from table top to top of lower panel) in. 32 + 16 Time required to retrieve a panel seconds 6 12

Lepto programs are very simple; each line of a Lepto script contains one or more complete statements. Blank lines and other whitespace are ignored, and comments will be like Python s and consist of a pound symbol (#) and everything after it on the same line. Table 23-1 explains the statements Lepto supports.

Similarly, for = 1 , the homogeneous linear system ( 1 I A)x = 0 is sin which reduces to j 1 1 j 1 0 j 0 x0 x1 x0 x1 = 0 0 ,

(Continued) Table 9.4. Tissue-speci c expression of NCS proteins as deduced from human UniGene database. VILIP-1 UniGene cluster Total no. EST sequences Pathological Other (pooled, unknown) No. EST sequences counted Tissue Brain Nerves Eye/optic nerve Heart Liver Spleen Lung Kidney Stomach Colon Skin Testis Ovary Placenta/uterus Glands. adrenal gland Pancreas Prostate Breast Hs.2288 196 23 15 158 (100%) 117 (74%) 14 (9%) 6 (4%) 1 (0.64%) 2 (1.3%) 3 (1.9%) 4 (2.5%) 1 (0.64%) 1 (0.64%) 2 (1.3%) 2 (1.3%) 1 (1.3%) 4 (2.5%) 1 (1.5%) 1 (0.6%) 5 (3%) 9 (5.6%) 5 (3%) 4 (2.5%) 6 (3.7%) Hippocalcin Hs.288654 96 26 3 67 (100%) 55 (82%) 1 (1.5%) 9 (13.4%) NCS-1 Hs.301760 299 121 19 161 (100%) 76 (47%) 10 (6%) 18 (11%) 6 (3.7%) 2 (1.2%) 7 (4.3%) 1 (0.6%) 4 (2.5%) 6 (3.7%)

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with a suf ciently high (e.g. above 10 MHz), and an amplitude of Vsweep large enough for covering the whole curve. In fact, many measurements of this type can be performed by starting the voltage sweep each time from a different bias point. A different curve is obtained for each bias point V0 , since the temperature and traps state of the device depends on the quiescent point only (Figure 3.27). In fact, the same curves can be measured by pulsing the voltage from the bias point for a short time to all points of the corresponding curve, one after the other, and measuring the current during the pulses. A typical set-up and a sequence of pulsed voltages and currents in the case of an FET are shown in Section 2.4, Figures 3.20 and 3.21. This arrangement is in fact the most common; this is why fast, isothermal and isotrap current measurements are also called pulsed measurements.