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Magnet/magnetism magnetic bead

Fig. 6.5 Schematic representation of a bioelectronic protocol for detection of DNA hybridization (A) binding of the target to magnetic beads (B) hybridization with CdS-labeled probe (C) dissolution of CdS tag (D) potentiometric stripping detection at a mercury-film electrode. (Reprinted from [136], Copyright 2009, with permission from Elsevier)... Fig. 6.5 Schematic representation of a bioelectronic protocol for detection of DNA hybridization (A) binding of the target to magnetic beads (B) hybridization with CdS-labeled probe (C) dissolution of CdS tag (D) potentiometric stripping detection at a mercury-film electrode. (Reprinted from [136], Copyright 2009, with permission from Elsevier)...
When the bacteria to be detected are less than 1% of the total population in a sample, IFAs cannot be used because of interference from unrelated particles that are concentrated when large volumes of sample are filtered. To overcome this problem, the organism of interest may be concentrated by immunomagnetic separation.10,51 62 For this procedure magnetic beads coated with monoclonal or polyclonal antibodies are mixed with the sample. The beads are collected with a magnet, and the cells attached to the beads then are removed, enumerated, and identified by IFAs. [Pg.7]

DNA,83 which produces one million or more copies of amplified DNA in a short time. For identification of bacteria, PCR can be used to amplify DNA either after extraction from a sample or after lysis of the cells.83,84 Methods using washing, filtration, or magnetic beads with specific antibodies can be used to collect bacterial cells for PCR.85,86 PCR can be modified for the detection of bacteria from various sources32 and can even amplify DNA from dead cells.87... [Pg.9]

S. Centi, S. Laschi, M. Franek, and M. Mascini, A disposable immunomagnetic electrochemical sensor based on functionalized magnetic beads and carbon-based screen-printed electrodes (SPCEs) for the detection of polychlorinated biphenyls (PCBs). Anal. Chim. Acta 538, 205—212 (2005). [Pg.166]

X. Zhao and S.A. Shippy, Competitive immunoassay for microliter protein samples with magnetic beads and near-infrared fluorescence detection. Anal. Chem. 76, 1871-1976 (2004). [Pg.401]

Anti-IgG attached magnetic beads O IgG j Carbon paste... [Pg.474]

FIGURE 14.5 Multiprotein electrical detection protocol based on different inorganic colloid nanocrystal tracers, (a) Introduction of antibody-modified magnetic beads (b) binding of the antigens to the antibodies on the magnetic beads (c) capture of the nanocrystal-labeled secondary antibodies (d) dissolution of nanocrystals and electrochemical stripping detection (reproduced from [29] with permission). [Pg.475]

FIGURE 14.6 Typical stripping voltammograms for (a) nanocrystal-labeled antibodies and (b-f) magnetic bead-Ab-Ag-Ab-nanocrystal complexes, (b) Response for a solution containing dissolved ZnS anti-/32-microglobulin, PbS-anti-BSA, and CdS-anti-IgG conjugates (reproduced from [29] with permission). [Pg.476]

Figure 11 The basic principle of ECL immunoassay using streptavidin-coated magnetic beads, and labels based on Ru(bpy)32+. Figure 11 The basic principle of ECL immunoassay using streptavidin-coated magnetic beads, and labels based on Ru(bpy)32+.
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.
Magnetically stimulated drug delivery systems, 9 57-61, 80-81 Magnetic bead-based immunoassays, 14 151... [Pg.544]

Micro- and nanobeads with magnetic properties have recently become popular since these tools can be manipulated, e.g., collected in the region of interest. Magnetite nanoparticles are introduced in order to render the polymeric beads magnetic. Preparation and application of magnetic beads will be discussed in more detail in Sect 5.5. [Pg.201]

Precipitation was found to be a very useful method for preparation of nanobeads with magnetic properties [17] since not only indicators but also small lipophilic magnetite nanobeads (having diameter of a few nanometers) can be incorporated inside the polymeric beads. Such multifunctional magnetic beads can be guided to the region of interest, be collected and manipulated there. [Pg.204]

Whenever the commercially available particles do not match the operator s requirements, a variety of possibilities exist in order to modify the particles from company suppliers. Similarly to other doped beads the dyes [92] or quantum dots [107, 108] can be physically entrapped into magnetic beads by swelling or are covalently bound to the surface of the particles. If localization of the dye on the particle surface is desired or if the polarity of dye and/or matrix polymer does not allow the irreversible entrapment of the dye in the bulk polymer, a covalent attachment of the dye is preferable [109, 110]. Even the covalent binding of whole fluorescent nanoparticles to magnetic microparticles is possible, as shown by Kinosita and co-workers who investigated the rotation of molecular motors [111]. [Pg.219]


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See also in sourсe #XX -- [ Pg.289 , Pg.291 , Pg.292 , Pg.389 , Pg.524 ]




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Antigens magnetic beads

Beads magnetic

Beads magnetic

Dynal’ magnetic beads

Functional magnetic beads

Magnetic Bead Characterization

Magnetic beads Dynabeads

Magnetic beads assays

Magnetic beads elution from

Magnetic beads preparation

Magnetic beads sample fractionation

Magnetic beads washing

Magnetic gel beads

Magnetic micro-bead mixer

Magnetic micro-beads

Magnetic molecularly imprinted beads

Monoclonal antibody-conjugated magnetic beads

Nanoparticle bead magnetic beads

Streptavidin-coated magnetic beads

Streptavidin-coupled magnetic beads

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