Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Label transfer reagents

The following sections describe three types of label transfer reagents, which are all built with a biotin handle. [Pg.1021]

Figure 28.14 A trifunctional label transfer reagent containing a thiol-reactive pyridyl disulfide group, a photo-reactive phenyl azide, and a biotin affinity tag. This compound can be used to label bait proteins through available thiol groups and capture interacting prey proteins by photoreactive conjugation. Figure 28.14 A trifunctional label transfer reagent containing a thiol-reactive pyridyl disulfide group, a photo-reactive phenyl azide, and a biotin affinity tag. This compound can be used to label bait proteins through available thiol groups and capture interacting prey proteins by photoreactive conjugation.
Figure 28.15 Two similar label transfer reagents containing a thiol-reactive methanethiolsulfonate group to label bait protein through available sulfhydryls, a tetrafluorophenyl azide group for high-efficiency photoreac-tive conjugation with interacting prey proteins, and a long biotin affinity tag. Figure 28.15 Two similar label transfer reagents containing a thiol-reactive methanethiolsulfonate group to label bait protein through available sulfhydryls, a tetrafluorophenyl azide group for high-efficiency photoreac-tive conjugation with interacting prey proteins, and a long biotin affinity tag.
Figure 28.11 Sulfo-SBED is a label transfer agent that contains a water-soluble sulfo-NHS ester to label bait proteins and a phenyl azide group for photoreactive capture of a prey protein. The biotin label can be used for detection or isolation of protein-protein conjugates using (strept)avidin reagents. The stars indicate the atoms that were used to measure the indicated molecular dimensions. Figure 28.11 Sulfo-SBED is a label transfer agent that contains a water-soluble sulfo-NHS ester to label bait proteins and a phenyl azide group for photoreactive capture of a prey protein. The biotin label can be used for detection or isolation of protein-protein conjugates using (strept)avidin reagents. The stars indicate the atoms that were used to measure the indicated molecular dimensions.
Dioxirane chemistry is well documented . Extensive kinetic, stereochemical and 0-labeling data suggested that dimethyldioxirane is the oxygen-atom transfer reagent in the Oxone-acetone system . Murray and Jeyaraman have shown that dialkyl dioxiranes can be isolated by low-temperature distillation from the reaction mixture of oxone and ketone . [Pg.1020]

Shake until dissolved. Then, adjust to the calibration mark with DDL Transfer contents of volumetric flask to a glass storage bottle and label MB Reagent. ... [Pg.553]

The response of a surface antigen-antibody reaction can also be mediated by an electron transfer reagent. This has been demonstrated by Robinson et al. in their studies on electrochemical immunoassays for hCG and thyroxine. In the analysis of hCG, a two-site amperometric immunoassay was developed in which monoclonal capture antibodies were immobilised on the surface of a glassy carbon electrode. A second antibody against hCG was labelled with glucose oxidase. The electrode was used both to separate free from bound enzyme-antibody conjugate and to assay the enzyme activity electrochemically by use of dimethylaminomethyl ferrocene as an electron transfer mediator. This method was found to correlate well with an immunoradiometric assay. In the analysis of thyroxine, another ferrocene derivative, namely ferrocenemonocarboxylic acid, was used as the electron transfer mediator. ... [Pg.369]

If the alkylaluminum labelled with C is used, the polymer contains C. Hydrogen acts as chain transfer reagents and the number of the active centers is not decreased as shown in Scheme 7.1 [26]. [Pg.116]

According to Elizarov [10b], there are four preparation stages of [ E]-labeled substances (1) concentration of the aqueous solution, mostly via ion exchange, of p E] produced in the cyclotron from 0-enriched water, (2) solvent exchange with phase transfer reagents, mostly from water to acetonitrile, (3) synthesis introduction of the [ E] fluoride ion, usually in a nucleophilic substitution, and (4) product isolation, either via HPLC with UV or radiometric detection or inline with prepacked cartridges. [Pg.140]


See other pages where Label transfer reagents is mentioned: [Pg.306]    [Pg.319]    [Pg.327]    [Pg.1020]    [Pg.1020]    [Pg.1020]    [Pg.1020]    [Pg.1020]    [Pg.1021]    [Pg.1023]    [Pg.1025]    [Pg.1027]    [Pg.1029]    [Pg.1031]    [Pg.306]    [Pg.319]    [Pg.327]    [Pg.1020]    [Pg.1020]    [Pg.1020]    [Pg.1020]    [Pg.1020]    [Pg.1021]    [Pg.1023]    [Pg.1025]    [Pg.1027]    [Pg.1029]    [Pg.1031]    [Pg.719]    [Pg.505]    [Pg.322]    [Pg.342]    [Pg.1025]    [Pg.1028]    [Pg.246]    [Pg.67]    [Pg.277]    [Pg.533]    [Pg.195]    [Pg.4175]    [Pg.796]    [Pg.141]    [Pg.32]    [Pg.142]    [Pg.351]    [Pg.21]    [Pg.1126]    [Pg.211]    [Pg.108]   
See also in sourсe #XX -- [ Pg.306 , Pg.1020 ]




SEARCH



Label reagents

Reagents labeled

Reagents labeling

Transfer reagent

Trifunctional Label Transfer Reagents

© 2024 chempedia.info