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Chip surface

Straight WC—Co tools are not suitable for machining steels that produce long chips because straight grades undergo crater wear from diffusion of WC into the steel chip surface. However, soHd solutions of WC—TiC, WC—TiC—TaC, etc, resist this type of chemical attack. In addition, tantalum carbide can improve thermal-shock resistance. Steel cutting compositions thus typically contain WC—TiC—(Ta,Nb)C—Co. Tantalum carbide is often added as (Ta,Nb)C because the chemical similarity between TaC and NbC makes their separation expensive. [Pg.445]

In physical objects involving thermal and fluid flow systems, the dual problem of how the heater is represented, and boiling as a local-instantaneous effect, should be considered. The temperature variations on the chip surface are a key characteristic of... [Pg.51]

In contrast to high density arrays low density arrays are made by deposition of pre-synthesized oligonucleotides or proteins on activated surfaces. There are several printing techniques for fabricating microarrays Non-contact biochip arrayers, commonly based on the piezoelectric effect, can apply controlled sub-nanoliter probe volumes to pre-specified locations on the chip surface. Due to the fact that the dispenser does not touch the surface, a non-contact arrayer provides low risk of contamination and is most suitable for printing on soft materials such as hydrogels. [Pg.483]

Important criteria for biomolecule immobilization are high functionality of the chip surface high immobilization capacity optimized density of functional groups stable linkage between the biomolecule and the solid support good accessibility for the interacting molecules low non-specific binding. [Pg.488]

Depending on the size of the probe, either covalent (Figures 10 and 11) or electrostatic immobilization (Figure 12) may be preferred. In general, oligonucleotides and DNA fragments of approximately 20 to 70 bases are amino-modified and bound covalently to the chip surface. Complete or partially complementary DNA of up to 5000 nucleotide bases is bound to the chip by electrostatic adsorption. [Pg.488]

Microelectronics arrays [8] Probes are drawn by electric current to chip surface Number of genes is dependent on the number of electrodes that can be made onto the surface of the array Fluorescent tag labeling and fluorescent detection Active Nanogen... [Pg.335]

Measor, P. Lunt, E. J. Seballos, L. Yin, D. Zhang, J. Z. Hawkins, A. R. Schmidt, H., On chip Surface enhanced Raman scattering (SERS) detection using integrated liquid core wave guides, Appl. Phys. Lett. 2007, 90, 211107... [Pg.511]

The fiber optic refractive index sensor finds use in biomedical applications. It uses a silicon chip with optical waveguides forming ring resonators. When the laser wavelength is scanned, the resonators cause dips in the power transmitted through the device. The wavelength at which these dips occur is a measure of the refractive index of the substance in contact with the chip surface. [Pg.429]

Although previous studies showed that direct ionization from the outlet separation channel at the chip surface with Taylor cone formation could be possible, this is probably not optimal because the ESI cone volumes are larger than peak volumes. With short... [Pg.497]

Fig. 3. SPR images of spots on the chip surface. White spots in SPR image illustrate 3-D NPH-SA or immobilized SA. The amounts of immobilized 3-D NPH-SA and SA were changed by SA concentrations in feed. Fig. 3. SPR images of spots on the chip surface. White spots in SPR image illustrate 3-D NPH-SA or immobilized SA. The amounts of immobilized 3-D NPH-SA and SA were changed by SA concentrations in feed.
The chip surface was repeatedly rinsed with water and ethanol. [Pg.229]

The main difficulty with this technology is the possible interaction of target and/or ap tamer with the chip surface. The nature of this difficulty may be high unspecific interaction or high repulsion. For this reason, the most suitable sensor chip surface and optimal binding conditions must be determined for every target/aptamer combination. [Pg.78]

Along this line Matsue et al. [37,45,78,79] have developed a number of biochips. Among them are multi-analyte assays for human placental lactogen (HPL) and human chorionic gonadotropin (HCG) [45] and leukocidin, a toxic protein produced by methicillin-resistant Staphylococcus aureus [79]. Figure 37.8 shows an example of a dual immunoassay with SECM detection. The analyte is defined by the position on the chip and the amount of analyte is quantified via the collection current at the UME. The current originates from the reduction of ferrocinium methanol (Fc+) at the UME. Fc+ is produced locally at the chip surface by the enzyme HRP under consumption of H202. [Pg.925]

More recently, another application of SECM detection in DNA and protein chips and in electrophoresis gels has emerged with different detection principles. Wang et al. [81] labeled single-stranded DNA (ssDNA) with gold nanoparticles. After binding to their complementary strand at the chip surface, silver was electroless deposited at the... [Pg.927]

Figure 11.4 Illustration of the SPR experiment. The binding of BACE to the immobilized small peptidic reference compound is detected by a change in refractive index at the chip surface. Preincubation of BACE with a test compound blocks the interaction with the immobilized reference compound in a manner that is dependent on the concentration of the test compound and its affinity for BACE. In practice, we could rank affinities by comparison of the SPR response at a fixed concentration of the test compound and then quantitatively determine the affinity by analyzing the concentration response dependence. In this example, the inhibitor in the middle panel (Inhibitor 1) has weaker affinity than the inhibitor in the lower panel (Inhibitor 2) because, at equivalent concentrations, Inhibitor 2 more extensively blocks the interaction between BACE and the immobilized peptidic inhibitor. Figure 11.4 Illustration of the SPR experiment. The binding of BACE to the immobilized small peptidic reference compound is detected by a change in refractive index at the chip surface. Preincubation of BACE with a test compound blocks the interaction with the immobilized reference compound in a manner that is dependent on the concentration of the test compound and its affinity for BACE. In practice, we could rank affinities by comparison of the SPR response at a fixed concentration of the test compound and then quantitatively determine the affinity by analyzing the concentration response dependence. In this example, the inhibitor in the middle panel (Inhibitor 1) has weaker affinity than the inhibitor in the lower panel (Inhibitor 2) because, at equivalent concentrations, Inhibitor 2 more extensively blocks the interaction between BACE and the immobilized peptidic inhibitor.

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See also in sourсe #XX -- [ Pg.224 ]

See also in sourсe #XX -- [ Pg.20 ]




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