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Threshold cycle

The concept of the threshold cycle (Ct) is the most important principle in TaqMan assays. Values are calculated for the amount of reporter dye released during each PCR cycle, and this is representative of the amount of the product amplified. The Ct is the cycle number at which the fluorescent signal from the reporter dye is first detected at a statistically significant level above the background [13]. The more template mRNA present at the beginning of the reaction, the lower the Ct will be needed to reach this threshold level of fluorescence. [Pg.12]

Onc-Factor-at-a-Timc Optimization One approach to optimizing the quantitative method for vanadium described earlier is to select initial concentrations for ITiOz and 1T2S04 and measure the absorbance. We then increase or decrease the concentration of one reagent in steps, while the second reagent s concentration remains constant, until the absorbance decreases in value. The concentration of the second reagent is then adjusted until a decrease in absorbance is again observed. This process can be stopped after one cycle or repeated until the absorbance reaches a maximum value or exceeds an acceptable threshold value. [Pg.669]

With the downhole power available and the signal detection threshold at surface, Figure 4-254b gives the maximum depth that can be reached by the technique as a function of frequency. Assuming that phase-shift keying is used with two cycles per bit, in a 10 fi m area (such as the Rocky mountains) a depth of 2 km (6,000 ft) could be reached while transmitting 7 bits/s. [Pg.942]

Plate 3. A snapshot of a Cyclic Cellular Automata (CCA) rule, which is a typical representative of a class of CA rules first introduced by David Griffeath (see http // psoup.math.wisc.edu/ kitchen.html). In this example, 14 colors are arranged cyclically. Bach color advances to the next, with the last color cycling back to 0. Each update of a site s color advances that color by 1 if there are at least a threshold number of sites of the next color within that site s neighbourhood. The example shown in this figure uses the 4-neighbor von Neumann neighbourhood. See Chapter 8. [Pg.158]

Theorem 5 [goles87a] If the synaptic-weight matrix A is symmetric, and the number of sites in the lattice is finite, then the orbits of the generalized threshold rule (equation 5.121) are either fixed points or cycles of period two. [Pg.277]

Although it is certainly not immediately obvious from the rule itself, it turns out that, just as is the case for generalized threshold rules, the only possible asymptotic states of finite symmetric muib -threshold rules are either fixed points or cycles of period two [golesQO]. Unlike their binary brethren, however, multi-threshold rules possess some intriguing additional properties. [Pg.284]

Sludge conditioners are required. Originally these were based on starches and lignins, but modem carbonate cycle treatments use carbonate-polymer programs, where the polymer (such as a phos-phinocarboxylic acid) provides a combination of threshold effect, crystal distortion, and sludge dispersion to minimize scaling and prevent sludge deposition. [Pg.413]

The relationship between load level and fatigue crack nucleation lives is clearly evident from the e-N and S-N plots for the material. A sample e-N plot for natural rubber is presented in Figure 25.4. An increase in the load level of the applied cycles results in a shorter fatigue life. Strain levels below the fatigue life threshold produce inhnite fatigue lives. The relationship between the load and the fatigue life follows a linear relation when plotted on a log-log scale. [Pg.677]

Figure 22 Real-time quantitation of PCR products. The straight line represents the threshold fluorescence value. Each curved line is a plot of the PCR products formed against the number of cycles for different samples. For samples containing 100% GMO, only B cycles are required to reach the threshold fluorescence. Samples containing 0.01% GMO will require F cycles before the threshold is attained... Figure 22 Real-time quantitation of PCR products. The straight line represents the threshold fluorescence value. Each curved line is a plot of the PCR products formed against the number of cycles for different samples. For samples containing 100% GMO, only B cycles are required to reach the threshold fluorescence. Samples containing 0.01% GMO will require F cycles before the threshold is attained...

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