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Transfer to a solid support

Figures 8 and 9 ow two specially designed multicompartment Langmuir troughs that permit the treatment of a monolayer with a series of different subphase reagent solutions, thus producing a known series of chemical reactions in the film. Following these treatments, the films may be transferred to a solid support or subjected to quantitative analysis to determine the outcome of the reactions. Figures 8 and 9 ow two specially designed multicompartment Langmuir troughs that permit the treatment of a monolayer with a series of different subphase reagent solutions, thus producing a known series of chemical reactions in the film. Following these treatments, the films may be transferred to a solid support or subjected to quantitative analysis to determine the outcome of the reactions.
The palladium-catalyzed coupling of boronic acids with aryl and alkenyl halides, the Suzuki reaction, is one of the most efficient C-C cross-coupling processes used in reactions on polymeric supports. These coupling reactions requires only gentle heating to 60-80 °C and the boronic acids used are nontoxic and stable towards air and water. The mild reaction conditions have made this reaction a powerful and widely used tool in the organic synthesis. When the Suzuki reaction is transferred to a solid support, the boronic add can be immobilized or used as a liquid reactant Carboni and Carreaux recently reported the preparation of the macroporous support that can be employed to efficiently immobilize and transform functionalized arylboronic adds (Scheme 3.12) [107, 246, 247]. [Pg.166]

Figure 8. Surface-plasmon microscopy, (a) The coupling of the incident photons to the surface mode can be accomplished by using a prism. The evanescent field of the surface plasmon extends into the monolayer coating, and the light that is scattered or diffracted when the resonance condition is not fulfilled can be imaged by the lens. After Rothenhausler and Knoll. (b) SPM images of a monolayer of DMPA in the LE-LC region transferred to a solid support. Figure 8. Surface-plasmon microscopy, (a) The coupling of the incident photons to the surface mode can be accomplished by using a prism. The evanescent field of the surface plasmon extends into the monolayer coating, and the light that is scattered or diffracted when the resonance condition is not fulfilled can be imaged by the lens. After Rothenhausler and Knoll. (b) SPM images of a monolayer of DMPA in the LE-LC region transferred to a solid support.
To detect specific sequences, DNA is usually transferred to a solid support, such as a sheet of nitrocellulose paper. For example, if bacteria are growing on an agar plate, cells from each colony will adhere to a nitrocellulose sheet pressed against the... [Pg.301]

Recently, liu et al. [33, 34] reported an absolute asymmetric transformation when the achiral monomer 10,12-tricosadiynoic acid was deposited on an aqueous solution containing Cu + ions. The monolayer was then transferred to a solid support as a Langmuir-Blodgett film, followed by photo-polymerization to yield a stable homochiral polydiacetylene as helical fibers. [Pg.206]

Monolayers floating in a liquid/gas (usually air) interface may be transferred to a solid support by the so-called LB technique. The procedure is to move a solid plate (various times) vertically through the monolayer while keeping the interfacial pressure constant, see Figure 7.8. [Pg.105]

Cholesterol crystallisation is thought to be the first step in the formation of gallstones in the human biliary system and the process of cholesterol nucleation remains incompletely understood. GIXD revealed a phase transition from a monolayer to a highly crystalline rectangular bilayer phase (165). The presence of the phospholipid DPPC in the cholesterol film inhibited cholesterol crystallisation [165]. AFM provided complementary information on the thickness and morphology of the cholesterol films transferred to a solid support The cholesterol monolayer thickness was 13 2 A and in the bilayer phase the presence of elongated faceted crystallites of pure cholesterol about 10 layers thick could be observed [165]. [Pg.242]

Figure 1. Some examples of luminescent probes with intramolecular charge transfer (ICT) electronic excited states. The numbers in parenthesis indicate the typical wavelengths of the excitation/emission maximums for each of them in polar media however, introduction of chemical groups in the unsubstituted molecular frame or attachment to a solid support may shift those values. Figure 1. Some examples of luminescent probes with intramolecular charge transfer (ICT) electronic excited states. The numbers in parenthesis indicate the typical wavelengths of the excitation/emission maximums for each of them in polar media however, introduction of chemical groups in the unsubstituted molecular frame or attachment to a solid support may shift those values.
The removal of highly lipophilic catalysts from the reaction product poses problems, which can be obviated by binding the ammonium Catalyst to a solid support. As well as being easily removed by nitration and recycled, such catalysts also have potential application in continuous flow phase-transfer catalytic processes. [Pg.19]

After electrophoresis, protein bands are transferred onto a solid support. Many aspects of a transfer can affect antigen detection. Some of these factors are specific to the transfer method and choice of membrane, whereas others apply to the entire blotting procedure. For example, the transfer efficiency may be affected by the presence of SDS in the gel and whether the gel was stained prior to transfer. [Pg.205]

In this approach, NAs are directly deposited onto a glass support using a robot able to deliver with high precision a sample to a specific x y programmed location. The NA sample is loaded into a spotting pin (highly miniaturized stainless-steel fountain-pen nibs with a gap) by capillary action, and small volumes are transferred to a solid surface, such as a microscope slide, by direct physical contact between the pin and the solid substrate. Spot size depends on the acceleration of the pen towards and away from the slide, and the surface tension of the slide. After the first spotting cycle, the pin is washed and a second sample is then transferred to an adjacent address. A robotic control system and multiplexed print heads allow the automated immobilization of many different probes simultaneously onto the slide [29]. [Pg.103]

The mode of deposition of a Langmuir film from the air/water interface to a solid- support is determined by the shape of the water miniscus during transfer at the interface. This shape is... [Pg.473]

Fig. 19 Reversible attachment of a Cu(I)-catalyst to a solid support via triple hydrogen bonds, acting as a reversible catalyst for atom transfer radical polymerization (ATRP)... Fig. 19 Reversible attachment of a Cu(I)-catalyst to a solid support via triple hydrogen bonds, acting as a reversible catalyst for atom transfer radical polymerization (ATRP)...
Figure 3 Methods for supported bilayer formation and membrane protein reconstitution, (a) and (b) LB/LS method. A lipid monolayer is spread at the air-water interface of a Langmuir trough and transferred to a solid substrate while keeping the surface pressure constant. A second monolayer is transferred by horizontal apposition of the first transferred monolayer and collection of a counter-piece with spacers, (c) Direct VF method. Membrane vesicles are flown into a chamber with a clean surface substrate on top. After about an hour of incubation, they form a supported bilayer on the substrate and excess vesicles are flushed out. (d) LB/VF method. The procedures depicted in panels (a) and (c) are combined leading to an asymmetric bilayer with an asymmetric protein distribution. Although this method can also be performed without a polymer, it is shown here with the polymer transferred during the LB step. Figure 3 Methods for supported bilayer formation and membrane protein reconstitution, (a) and (b) LB/LS method. A lipid monolayer is spread at the air-water interface of a Langmuir trough and transferred to a solid substrate while keeping the surface pressure constant. A second monolayer is transferred by horizontal apposition of the first transferred monolayer and collection of a counter-piece with spacers, (c) Direct VF method. Membrane vesicles are flown into a chamber with a clean surface substrate on top. After about an hour of incubation, they form a supported bilayer on the substrate and excess vesicles are flushed out. (d) LB/VF method. The procedures depicted in panels (a) and (c) are combined leading to an asymmetric bilayer with an asymmetric protein distribution. Although this method can also be performed without a polymer, it is shown here with the polymer transferred during the LB step.
FK5.6.I9 Schematic representation of the structural formation and order-disorder transition for photoactive LBK showing (A) the compressed monolayer on the water surface with densely packed chromophore side chains oriented into the gas phase and the polymer backbone facing the water surface, and (B) LBK transfer from the water to a solid support, resulting in well-ordered smetic-tike (bilayered) multilayer assemblies. (C) After phcnoinduced trars to cts isomerization, a largely disordered struaure is obtained and the layered structure is completely lost (reproduced from reference 72 with permission from Wifey-VCH). [Pg.203]

The synthesis of a CMP-NeuAc derivative that was bound to a solid support through the 9-position of the sialic acid has been reported by the Kajihara group [47]. This derivative is quite useful in that it can be utilized to immobilize glycoproteins onto a solid support by transferring the sialic acid to the terminus of the carbohydrate chain of the glycoprotein. [Pg.204]

Since the Reimer-Tiemann reaction always yields a mixture of ortho- and para-substituted phenols whenever the two positions are unsubstituted (and sometimes even when the positions are substituted, see carboxy-substituted phenols), it is not surprising that attempts have been made to increase the regioselectivity. Earlier attempts (for details, see reviews) emphasized the nature of the cation, the solvent, or used phase-transfer catalysis. Recent studies have concentrated on the use of cyclodextrins as base-stable host compounds, permitting exclusive para substitution. Attaching the cyclodextrins to a solid support has also been attempted, a natural step in view of the high cost of the cyclodextrins and the need for cheap product i.e. p-hydroxybenzaldehyde). p-Hydroxybenzaldehyde has been prepared in 59-65% yield using P-cyclodextrin that has been immobilized with epichlorohydrin. TTie catalyst is easily recovered and can be reused without appreciable loss of activity. [Pg.771]

In the Eastern-Western procedure, lipids are first applied to a solid support such as nitrocellulose. Next, proteins subjected to sodium dodecyl sulfate polyacrylamide gel electrophoresis are transferred by standard Western blotting techniques to the solid support in such a manner that the protein of interest is transferred to the lipid patch. During electrotransfer of protein to the solid support, protein, lipid, and sodium dodecyl sulfate mix and as transfer continues the sodium dodecyl sulfate is removed leaving behind the protein to refold in the presence of lipid. Attachment of the refolded protein to a solid support allows one to probe protein structure using conformation-sensitive antibodies or protein function... [Pg.27]


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See also in sourсe #XX -- [ Pg.177 ]

See also in sourсe #XX -- [ Pg.177 ]




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