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Hairpin-Caged MO

The DMNB hairpin cMOs have been applied to the knockdown of several genes, including no tail a ntla), heart of glass (heg), floating head iflh), and ETSl-related protein (etv2) [5, 6]. They also helped reveal an important regulatory mechanism in embryo development, as discussed in Section 23.4. [Pg.342]

Apart from UV-cleavable DMNB linkers, a bromohydroxyquinoline (BHQ) linker was also introduced into hairpin cMOs, which enables two-photon activation of MO function at 750 nm [6]. This BHQ linker can provide improved spatial resolution and is less likely to cause any phototoxicity because of UV exposure. [Pg.342]


Figure 23.3 Different strategies to pho-tochemlcally control MO function, (a) Hairpin-caged MO with a dimethoxyni-trobenzyi (DMNB) or bromohydroxyquino-iine (BHQ) iinker. (b) Sense-caged MO with an o-nitrobenzyi (ONB) iinker. (c) Nucieobase-caged MO biocked with... Figure 23.3 Different strategies to pho-tochemlcally control MO function, (a) Hairpin-caged MO with a dimethoxyni-trobenzyi (DMNB) or bromohydroxyquino-iine (BHQ) iinker. (b) Sense-caged MO with an o-nitrobenzyi (ONB) iinker. (c) Nucieobase-caged MO biocked with...

See other pages where Hairpin-Caged MO is mentioned: [Pg.340]    [Pg.341]   


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