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Maleimide biotin-BMCC

Figure 11.8 Biotin-BMCC provides sulfhydryl reactivity through its terminal maleimide group. The reaction creates a stable thioether linkage. Figure 11.8 Biotin-BMCC provides sulfhydryl reactivity through its terminal maleimide group. The reaction creates a stable thioether linkage.
The reagent is similar to another maleimide-containing biotinylation reagent, 3-(N-maleimi-dopropionyl) biocytin, a compound used to detect sulfhydryl-containing molecules on nitrocellulose blots after SDS-electrophoresis separation (Bayer et al., 1987). Biotin-BMCC should be useful in similar detection procedures. [Pg.521]

Fig. 8.5. Specific example of an RNA catalyzed reaction [4 + 2] Diels-Alder cycloaddition between an RNA-tethered diene and a biotin-linked maleimide dienophile (BMCC-biotin). Cycloaddition creates an affinity-tagged (biotin) RNA product that can be captured and purified. Fig. 8.5. Specific example of an RNA catalyzed reaction [4 + 2] Diels-Alder cycloaddition between an RNA-tethered diene and a biotin-linked maleimide dienophile (BMCC-biotin). Cycloaddition creates an affinity-tagged (biotin) RNA product that can be captured and purified.

See other pages where Maleimide biotin-BMCC is mentioned: [Pg.520]    [Pg.521]    [Pg.668]    [Pg.990]    [Pg.404]    [Pg.680]    [Pg.384]    [Pg.660]   
See also in sourсe #XX -- [ Pg.520 ]

See also in sourсe #XX -- [ Pg.384 ]

See also in sourсe #XX -- [ Pg.384 ]




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