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Unbounded Regions

Fig. 1. Southern blot analysis of DNA showing (a) step 1, an agarose gel containing separated restriction fragments of DNA, denoted by (—), which is immersed in NaOH to denature the double-stranded stmcture of DNA, and then transferred by capillary flow to a nitrocellulose filter. In step 2, the bound DNA is allowed to hybridize to a labeled nucleic acid probe, and the unbound probe is washed off In step 3, the filter is placed into contact with x-ray film resulting in (b) bands of exposure on the film which are detected after development and correspond to regions where the restriction fragment is... Fig. 1. Southern blot analysis of DNA showing (a) step 1, an agarose gel containing separated restriction fragments of DNA, denoted by (—), which is immersed in NaOH to denature the double-stranded stmcture of DNA, and then transferred by capillary flow to a nitrocellulose filter. In step 2, the bound DNA is allowed to hybridize to a labeled nucleic acid probe, and the unbound probe is washed off In step 3, the filter is placed into contact with x-ray film resulting in (b) bands of exposure on the film which are detected after development and correspond to regions where the restriction fragment is...
We have seen that the output neuron in a binary-threshold perceptron without hidden layers can only specify on which side of a particular hyperplane the input lies. Its decision region consists simply of a half-plane bounded by a hyperplane. If one hidden layer is added, however, the neurons in the hidden layer effectively take an intersection (i.e. a Boolean AND operation) of the half-planes formed by the input neurons and can thus form arbitrary (possible unbounded) convex regions. ... [Pg.547]

Figure 8 Chemiluminescent (A and B) and bioluminescent (C) detections for immobilized hybridizations of PCR product. Dg, digoxigenin Bt, biotin Ad, avidin. Procedure A [30] Biotin moiety is incorporated into PCR products during the amplification reaction, using one 5 -biotinylated primer. The product is hybridized with a Dg-labeled probe and is immobilized on streptavidin-coated magnetic beads. This capture reaction is carried out for 30 min at 37°C. A permanent magnet is used to sediment the beads during washing to remove unbound DNA. By incubation with the washed beads for 45 min at 37°C, anti-Dg antibody conjugated to HRP enzyme is bound to the Dg-labeled probe, and luminol reaction is performed for CL detection. Procedure B [31] Wells of apolystyrene microtiter plate are activated with l-ethyl-3-(3-dimethylaminopropyl)-carbodiimide, and then coated with a labeled cDNA probe complementary to an internal region of the target DNA. Figure 8 Chemiluminescent (A and B) and bioluminescent (C) detections for immobilized hybridizations of PCR product. Dg, digoxigenin Bt, biotin Ad, avidin. Procedure A [30] Biotin moiety is incorporated into PCR products during the amplification reaction, using one 5 -biotinylated primer. The product is hybridized with a Dg-labeled probe and is immobilized on streptavidin-coated magnetic beads. This capture reaction is carried out for 30 min at 37°C. A permanent magnet is used to sediment the beads during washing to remove unbound DNA. By incubation with the washed beads for 45 min at 37°C, anti-Dg antibody conjugated to HRP enzyme is bound to the Dg-labeled probe, and luminol reaction is performed for CL detection. Procedure B [31] Wells of apolystyrene microtiter plate are activated with l-ethyl-3-(3-dimethylaminopropyl)-carbodiimide, and then coated with a labeled cDNA probe complementary to an internal region of the target DNA.
A vector x is feasible if it satisfies all the constraints. The set of all feasible points is called the feasible region F. If F is empty, the problem is infeasible, and if feasible points exist at which the objective/is arbitrarily large in a max problem or arbitrarily small in a min problem, the problem is unbounded. A point (vector) x is termed a local extremum (minimum) if... [Pg.118]

The definitions of convexity and a convex function are not directly useful in establishing whether a region or a function is convex because the relations must be applied to an unbounded set of points. The following is a helpful property arising from the concept of a convex set of points. A set of points x satisfying the relation... [Pg.127]

Two additional cases can exist. First, if the constraint x1 + x2 2 had been removed, the feasible region would appear as in Figure 7.2, that is, the set would be unbounded. Then max/is also unbounded because/can be made as large as desired subject to the constraints. Second, at the opposite extreme, the constraint set could be empty, as in the case where xx + x2 < 2 is replaced by x + x2 < — 1. Thus an LP problem may have (1) no solution, (2) an unbounded solution, (3) a single optimal solution, or (4) an infinite number of optimal solutions. The methods to be developed deal with all these possibilities. [Pg.224]

Consider first an unbounded domain and ajtotally reflecting surface. To obtain an expression for Pj, we assume that the presence of the boundary at z = 0 can be accounted for by adding the concentration resulting from an imaginary source at z = -z to that from the source at z = z in the region z 0. Then assumes the form... [Pg.236]

The z boundary conditions specify both the extent of the region and the physical interaction of the material with the boundaries. It will be convenient in solving Eq. (5.14) to assume that an impermeable barrier to diffusion exists at a height z = H. Then the case of an unbounded region z 0 is obtained by letting //—> < . The surface (z = 0) boundary condition can be represented in general as... [Pg.238]

Dissociation occurring by tunneling from a bound to an unbound rovibronic state (i.e., a state corresponding to a particular rotational energy level of a vibrational level of an electronic state). 2. The appearance of a diffuse band region within a series of sharp bands of an absorption spectrum. [Pg.570]

The unique spectra of either Aj or Aj- could be detected in unbound PsaC where cysteine II in the consensus iron-sulfur binding site was changed to Asp, Gly, Ala, 88 314324. in this case the altered cluster is suggested to be in a high spin state (S > 3/2) and is therefore not detectable in the g = 2 region of the EPR spectra, where pure spectra of unchanged iron sulfur clusters in a low spin state (S = 1/2) could be observed. The unique spectra of FA- and FB could also be observed in the fully assembled PS I, which was dark-frozen in the presence of ascorbate and illuminated under cryogenic temperatures inside the EPR cavity (for review see reference 188). [Pg.206]


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See also in sourсe #XX -- [ Pg.133 , Pg.134 , Pg.135 , Pg.136 , Pg.236 ]




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Unbounded

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