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Clustering of channels

In each trace in Figure 6.2, after several seconds of exposure to ACh it becomes possible to identify individual clusters of AChR channel openings. Analysis of these clusters of channel openings, as illustrated in Figure 6.3, allows the relationship between ACh concentration andpopm to be determined. [Pg.190]

Using the freeze fracture technique, electron microscopy and laser scanning confocal microscopy, it became obvious that these gap junctional channels are arranged as a cluster of channels with about 50 channels within one disk as stated by Gourdie et al. [1990]. [Pg.17]

The rate of exocytosis from any type of cell is a very important factor and is therefore subject to strict regulation. This rate can be changed through the modification of different parameters of the exocytotic machinery. Analysis of pancreatic /J-cells shows that the latency time in the Ca2+ sensing system of the exocytotic machinery and the clustering of channels on the cell surface may be two convenient targets for adjusting the rate of the release of hormones or neurotransmitters from cells. [Pg.311]

FIGURE 6-32 Molecular structure of (a) gap junctions, (a) Schematic model of a gap Junction, which comprises a cluster of channels between two plasma membranes separated by a gap of about 2-3 nm. Both membranes contain connexon hemichannels, cylinders of six dumbbellshaped connexin molecules. Two connexons Join in the gap between the cells to form a gap-junction channel,... [Pg.230]

B. thurigiensis is a common Gram-positive, spore-forming soil bacterium that produces inclusion bodies, microcrystalline clusters of many different proteins. These crystalline proteins, called 5-endotoxins, are the ion channel toxins that are sold commercially for pest control. Most such endotoxins are protoxins, which are inactive until cleaved to smaller, active proteins by proteases in the gut of a susceptible insect. One such crystalline protoxin. [Pg.275]

Fig. 2.33a-c Boiling in the central part of microchannels. Tls = 0.14 m/s, q = 220 kW/m. 1 Clusters of liquid droplets at the bottom of the channel. 2 Clusters of the liquid droplets on the side-wall. 5 Steam. Reprinted from Hetsroni et al. (2003b) with permission... [Pg.49]

Figure 2.40 shows the unsteady flow upstream of the ONE in one of the parallel micro-channels of d = 130 pm at = 228kW/m, m = 0.044 g/s (Hetsroni et al. 2001b). In this part of the micro-channel single-phase water flow was mainly observed. Clusters of water appeared as a jet, penetrating the bulk of the water (Fig. 2.40a). The vapor jet moved in the upstream direction, and the space that it occupied increased (Fig. 2.40b). In Fig. 2.40a,b the flow moved from bottom to top. These pictures were obtained at the same part of the micro-channel but not simultaneously. The time interval between events shown in Fig. 2.40a and Fig. 2.40b is 0.055 s. As a result, the vapor accumulated in the inlet plenum and led to increased inlet temperature and to increased temperature and pressure fluctuations. Figure 2.40 shows the unsteady flow upstream of the ONE in one of the parallel micro-channels of d = 130 pm at = 228kW/m, m = 0.044 g/s (Hetsroni et al. 2001b). In this part of the micro-channel single-phase water flow was mainly observed. Clusters of water appeared as a jet, penetrating the bulk of the water (Fig. 2.40a). The vapor jet moved in the upstream direction, and the space that it occupied increased (Fig. 2.40b). In Fig. 2.40a,b the flow moved from bottom to top. These pictures were obtained at the same part of the micro-channel but not simultaneously. The time interval between events shown in Fig. 2.40a and Fig. 2.40b is 0.055 s. As a result, the vapor accumulated in the inlet plenum and led to increased inlet temperature and to increased temperature and pressure fluctuations.
Figure 6.18d shows the appearance of liquid droplets or clusters of liquid droplets on the wall after the bubble venting. The pressure in the micro-channel decreases and water starts to move into it from the inlet manifold (Fig. 6.18e). Figure 6.18f shows the start of a new cycle. [Pg.283]

In the preparation of Mo/KL, the addition of 1 was stopped when pH of the solution was lowered to about 3. The resulting Mo/KL contained only 2.1 wt% (74% of added molybdenum clusters) of molybdenum. Chlorine was absent, which indicates that the cluster 1 acted as a tetravalent cation. The LTL structure is characterized by a monodimensional system of channels, whose diameter (0.70 nm) [14] is close to the size of the cluster 1. It is conceivable that, once the cluster 1 was incorporated into an LTL main channel and present at a site near the external surface, the sites deep in the channel are no more accessible to another cluster. [Pg.110]

By swelling with aqueous electrolyte, cations (and, to lesser extent, also anions) penetrate together with water into the hydrophilic regions and form spherical electrolyte clusters with micellar morphology. The inner surface of clusters and channels is composed of a double layer of the immobilized —SO3 groups and the equivalent number of counterions, M+. Anions in the interior of the clusters are shielded from the —SOJ groups by hydrated cations and water molecules. On the other hand, anions are thus... [Pg.144]

Fig. 20. Diagram showing a singlelength channel and a doublelength channel formed across a phospholipid bilayer by a circular cluster of nystatin or amphotericin B aggregates... Fig. 20. Diagram showing a singlelength channel and a doublelength channel formed across a phospholipid bilayer by a circular cluster of nystatin or amphotericin B aggregates...
Bulbophyllum vaginatum Reich, f. is an epiphytic orchid that grows in Thailand, Indonesia, and Malaysia. The stems are 3 mm in diameter. The petiole is 2 X 6 mm, swollen, and deeply channeled. The blade is elliptic, thick, spongy, and 8x3 cm. The flowers are arranged in clusters of 12-15 pale yellow, 5-cm-long flowers with elongated corollas (Fig. 57). [Pg.114]

Ishibashi, T., Dupree, J. L., Ikenaka, K. et al. A myelin galac-tolipid, sulfatide, is essential for maintenance of channels on myelinated axons but not essential for initial cluster formation. /. Neurosci. 22 6507-6514, 2002. [Pg.48]


See other pages where Clustering of channels is mentioned: [Pg.52]    [Pg.189]    [Pg.191]    [Pg.228]    [Pg.31]    [Pg.1116]    [Pg.492]    [Pg.310]    [Pg.143]    [Pg.97]    [Pg.52]    [Pg.189]    [Pg.191]    [Pg.228]    [Pg.31]    [Pg.1116]    [Pg.492]    [Pg.310]    [Pg.143]    [Pg.97]    [Pg.89]    [Pg.152]    [Pg.555]    [Pg.664]    [Pg.50]    [Pg.32]    [Pg.51]    [Pg.459]    [Pg.67]    [Pg.322]    [Pg.190]    [Pg.190]    [Pg.190]    [Pg.191]    [Pg.191]    [Pg.15]    [Pg.183]    [Pg.184]    [Pg.184]    [Pg.185]    [Pg.186]    [Pg.451]    [Pg.29]    [Pg.106]    [Pg.106]    [Pg.281]    [Pg.299]   
See also in sourсe #XX -- [ Pg.311 ]




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