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Gel matrices

The apphcation of an electric field to a gel matrix or capillary tube results in heating in the media and gassing at the electrodes. Thus special attention in the design and use of electrophoretic equipment is required. [Pg.178]

Problems associated with gel-to-gel variabiUty have been rectified with the advancement of ampholyte mixtures. One commonly used mixture of ampholytes, called Immobilines, is an improved ampholyte mixture that produces no gradient drift or unequal pH gradient (26) and can be used in a gel matrix reproducibly from one day to the next. [Pg.181]

The tissue to be analyzed is placed directiy onto the gel. Using the tissue itself and not tissue extracts has advanced the study of proteins that are difficult to extract from tissue, or are damaged by the extraction procedure. Dtif is an important advancement in the area of sample handling and appHcation where direct appHcation of a soHd to a gel matrix may actually enhance resolution. [Pg.181]

Paper Electrophoresis. Paper (qv) as an electrophoretic matrix was employed in some of the first electrophoretic techniques developed to separate compounds. Paper is easier than a gel matrix because the paper matrix requires no preparation. Besides being easy to obtain, paper is a good medium because it does not contain many of the charges that interfere with the separation of different compounds. Two types of paper employed in this type of electrophoresis are Whatman 3 MM (0.3 mm) and Whatman No. 1 (0.17 mm). [Pg.182]

In this lecture we will be concerned by exocytosis of neurotransmitters by chromaffin cells. These cells, located above kidneys, produce the adrenaline burst which induces fast body reactions they are used in neurosciences as standard models for the study of exocytosis by catecholaminergic neurons. Prior to exocytosis, adrenaline is contained at highly concentrated solutions into a polyelectrolyte gel matrix packed into small vesicles present in the cell cytoplasm and brought by the cytoskeleton near the cell outer membrane. Stimulation of the cell by divalent ions induces the fusion of the vesicles membrane with that of the cell and hence the release of the intravesicular content into the outer-cytoplasmic region. [Pg.10]

The producer of column No. 6 tried to supplementary remove admixtures from the gel matrix by applying liquid extractions. He revealed that the extraction process was very slow and that the apparently clean material started to bleed again after some time or when the temperature of extraction was raised. This result indicates that the retention properties of SEC columns may change in the course of their use as a result of cleaning their surface. Maybe the recipes for the gel synthesis will have to be modified to suppress the effects of additives. It seems that the producer of column No. 5 is not far from the ideal situation, at least for the PMMA-toluene system. We cannot exclude... [Pg.456]

Classical gel electrophoresis has been used extensively for protein and nucleic acid purification and characterization [9, 10], but has not been used routinely for small molecule separations, other than for polypeptides. A comparison between TLC and electrophoresis reveals that while detection is usually accomplished off-line in both electrophoretic and TLC methods, the analyte remains localized in the TLC bed and the mobile phase is immediately removed subsequent to chromatographic development. In contrast, in gel electrophoresis, the gel matrix serves primarily as an anti-... [Pg.289]

It is interesting that this cement has been known for over 100 years and yet certain features of its chemistry remain obscure. The exact nature of the matrix is still a matter for conjecture. It is known that the principal phase is amorphous, as a result of the presence of aluminium in the liquid. It is also known that after a lapse of time, crystallites sometimes form on the surface of the cement. A cement gel may be likened to a glass and this process of crystallization could be likened to the devitrification of a glass. Therefore, it is reasonable to suppose that the gel matrix is a zinc aluminophosphate and that entry of aluminium into the zinc phosphate matrix causes disorder and prevents crystallization. It is not so easy to accept the alternative explanation that there are two amorphous phases, one of aluminium phosphate and the other of zinc phosphate. This is because it is difficult to see how aluminium could act in this case to prevent zinc phosphate from crystallizing. [Pg.211]

The silica gel matrix for the RP-18 PLC precoated plates consists either of a type 60 or 150 (indicating the respective mean pore diameter). The manufacturers and the properties of the PLC plates RP-18 available at present are listed in Table 3.8. [Pg.58]

Colloids embedded in a silica sol-gel matrix were prepared by using fully alloyed Pd-Au particles. The Mossbauer data have yielded evidence that alloying Pd with Au in bimetallic colloids leads to enhanced catalytic hydrogenation and also to improved selectivity [426]. [Pg.364]

Figure 5.1.7 shows the propagator of the motion measured for a clean and a biofilm impacted capillary [14,15] and the residence time distributions calculated for each from these velocity distributions. The clean capillary gives an experimental propagator equal to the theoretical velocity distribution convolved with a Gaussian diffusion curve [14], as shown in Figure 5.1.2. For the flow around the biofilm structure note the appearance of a high velocity tail indicating higher probability of large displacements relative to the clean capillary. The slow flow peak near zero displacement results from the protons trapped within the EPS gel matrix where the... Figure 5.1.7 shows the propagator of the motion measured for a clean and a biofilm impacted capillary [14,15] and the residence time distributions calculated for each from these velocity distributions. The clean capillary gives an experimental propagator equal to the theoretical velocity distribution convolved with a Gaussian diffusion curve [14], as shown in Figure 5.1.2. For the flow around the biofilm structure note the appearance of a high velocity tail indicating higher probability of large displacements relative to the clean capillary. The slow flow peak near zero displacement results from the protons trapped within the EPS gel matrix where the...
The scheme below shows reaction possibilities for carbonyldiimidazole activation of polyhydroxylic matrices. The formation of these activated sites depends on[117] 1. the partial disposition of hydroxyl groups accessible to the solvent, 2. the initial concentration of CDI, and 3. the chemical nature of the gel matrix. [Pg.170]

Concerning drug delivery, electrically erodible polymer gels for controlled release of drugs have been prepared, and a measured release rate of insulin has been observed under electrical stimulus [69]. A suspension of zinc insulin in a mixed solution of poly(ethyloxazoline) and PMAA was formed into a gel by decreasing the pH of the suspension. The obtained complex gel with 0.5 wt% of insulin was attached to a woven platinum wire cathode which was 1 cm away from the anode and immersed in 0.9% saline solution. When a stepped function of electrical current of 5 mA was applied to the insulin-loaded gel matrix, insulin was released in a stepwise manner up to a release of 70%. The insulin rate measured was 0.10 mg/h. [Pg.159]

Scheme 5.10 The use oftwo otherwise incompatible catalysts enabled by their immobilization in a sol-gel matrix (SC) to perform a two-step cascade [25],... Scheme 5.10 The use oftwo otherwise incompatible catalysts enabled by their immobilization in a sol-gel matrix (SC) to perform a two-step cascade [25],...

See other pages where Gel matrices is mentioned: [Pg.206]    [Pg.452]    [Pg.453]    [Pg.473]    [Pg.184]    [Pg.2063]    [Pg.311]    [Pg.235]    [Pg.456]    [Pg.227]    [Pg.12]    [Pg.73]    [Pg.555]    [Pg.92]    [Pg.478]    [Pg.101]    [Pg.52]    [Pg.305]    [Pg.305]    [Pg.660]    [Pg.281]    [Pg.263]    [Pg.529]    [Pg.591]    [Pg.402]    [Pg.403]    [Pg.407]    [Pg.408]    [Pg.706]    [Pg.706]    [Pg.574]    [Pg.429]    [Pg.143]   
See also in sourсe #XX -- [ Pg.289 ]

See also in sourсe #XX -- [ Pg.289 ]

See also in sourсe #XX -- [ Pg.806 ]

See also in sourсe #XX -- [ Pg.333 ]




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Agarose gel matrix

Alumina sol-gel matrices

Biomolecules, interactions and stability in sol-gel matrices

Collagen-gel matrix

Encapsulation in Sol-Gel Matrices

Entrapment in Gel Matrixes

Gel Matrices for Size Exclusion Chromatography

Gel matrix concentration

Gel matrix tablets

Plant and animal whole cells, in sol-gel matrices

Polymer gel matrix

Silica sol-gel matrix

Sol-gel chemistry and matrix characteristics

Sol-gel matrices

Sol-gel matrices advantages and disadvantages

Sol-gel matrices applications

Sol-gel matrices biocompatibility and conductivity

Sol-gel matrices carbon-ceramic electrodes

Sol-gel matrices characteristics

Sol-gel matrices electrochemical biosensors

Sol-gel matrices electrode surface coatings

Sol-gel matrices enzyme-based biosensors

Sol-gel matrices immunoaffinity columns

Sol-gel matrices immunosensors

Sol-gel matrices interactions and biomolecules stability

Sol-gel matrices microbial cells

Sol-gel matrices optical biosensors

Sol-gel matrices photoactive proteins-based biosensors

Sol-gel matrices plant and animal cells

Sol-gel matrices porosity and proteins dynamics

Sol-gel matrices progress

Sol-gel matrices whole-cell encapsulation

The Electrical Contacting of Enzymes in Mediator-functionalized Sol-gel Matrices

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