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Collecting duplex

The primary conclusion that follows from the effect of base sequence on the efficiency of radical cation migration through duplex DNA is that base pairs cannot be considered in isolation. For example, the effect of placing a T in a sequence of purines depends critically on the nature and number of purines. In this regard, the effect of base sequence on radical cation transport emerges from examination of collective properties of the DNA. This is a clear indication that the charge is delocalized over several base pairs, a conclusion that is supported by extensive quantum calculations. [Pg.167]

Following incubation, add an equal volume of 10% TCA to the reaction mixture. Mix and cool to about 5° for 1 hr. Collect the precipitates, which are the SI-resistant duplexed DNA fragments, on nitrocellulose filters, dry, and count for radioactivity. [Pg.344]

PCR requires a thermostable DNA polymerase, nucleotides of each base (collectively referred to as dNTPs)y the target sequence, and a pair of oligonucleotides (referred to as primers) complementary to opposite strands flanking the sequence to be detected. In the first step, target duplexes are denatured into single strands by heat (Figure 37-2). When the mixture is cooled, primers provided in great excess (usually over a miUion times the concentration of the initial... [Pg.1412]

Pass again on hydroxyapatite but collect cDNA RNA duplex. Add NaOH to 0.1 N, heat to 65°C and neutralize with 2 M Tris-HCl (pH 7.5) and wash with TRES save 10% of cDNA for screening. [Pg.276]

Figure 25. Left Base stacking in double-stranded DNA (only one strand shown) Right Determination of thermodynamic parameters of duplex formation Oligonucleotides 3 -dA(U]-A(MEQ1-5 and T 12) were diluted starting from 9 pM to 4.5 pM in 0.15 M NaCl, 0.01 M Tris-HCl, pH 7.0,25 °C and hybridization data were collected. From [149],... Figure 25. Left Base stacking in double-stranded DNA (only one strand shown) Right Determination of thermodynamic parameters of duplex formation Oligonucleotides 3 -dA(U]-A(MEQ1-5 and T 12) were diluted starting from 9 pM to 4.5 pM in 0.15 M NaCl, 0.01 M Tris-HCl, pH 7.0,25 °C and hybridization data were collected. From [149],...
In the cokeless cupola, the metal charge is heated by the combustion of natural gas. Instead of the traditional coke bed, a bed of refractory spheres on a water-cooled grid supports the metal charge. The molten metal droplets run through this bed and are collected in the well at the bottom of the furnace. The life of the spheres exposed to the superfieating temperatures of the metal is limited. A cokeless cupola is therefore run at a reduced temperature (1400 "C instead of 1500 C) and superheating of the liquid metal is done in an attached gas-fired or induction furnace (duplex operation). [Pg.165]

Fig. 3. A, "Slipped" circle formation by denaturation and annealing of a permuted collection of DNA duplexes. Notice that in the permuted DNA molecules the circular order of genes is constant, but the ends are repetitious. However, different DNA duplexes may have different repetitious ends. Upon annealing, the single strand fragments at either end of the same linear duplex may contain complementary sequences, which can undergo further reannealing to produce a circular duplex molecule. In some cases the single-stranded regions at the ends of the linear duplex will not be complementary and so will not result in circular duplex structures. (From Thomas. 1967. J. Cell Physio ., 70 (Suppl. 1) 13-34.)... Fig. 3. A, "Slipped" circle formation by denaturation and annealing of a permuted collection of DNA duplexes. Notice that in the permuted DNA molecules the circular order of genes is constant, but the ends are repetitious. However, different DNA duplexes may have different repetitious ends. Upon annealing, the single strand fragments at either end of the same linear duplex may contain complementary sequences, which can undergo further reannealing to produce a circular duplex molecule. In some cases the single-stranded regions at the ends of the linear duplex will not be complementary and so will not result in circular duplex structures. (From Thomas. 1967. J. Cell Physio ., 70 (Suppl. 1) 13-34.)...
At the start of a measurement session, a white-light spectrum is necessary. The white source can be switched into position under software control. A dark set is automatically recorded and subtracted from the white set. Figure 12A shows a typical result for the two simultaneously recorded stripes of the spectrum obtained with a Kaiser Optical Holoprobe 532 nm system with a duplex grating. For this recording, the white source was placed at the sample position so that the effect of the full collection path was recorded. [Pg.285]

Duplex Collecting Systems 109 Etiology and Epidemiology 109 Presentation and Circumstances of Diagnosis 109... [Pg.89]


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