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Clontech/iDimerize inducible protein dimerization in vivo/5 mg/635055

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品牌:Clontech
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iDimerize inducible protein dimerization in vivo in trangenic mice

Many in vitro applications for chemical-induced dimerization (CID) have progressed into transgenic animals. The B/B Homodimerizer (AP20187) has been the most widely used in vivo, and typically investigators have used doses of 0.5–10 mg per kg for each injection. At this dosage, 5 mg of dimerizer is sufficient for 20–400 injections for a 25-gram mouse. However, the exact dose and treatment must be determined empirically for each experiment.

Many in vitro applications for chemical-induced dimerization (CID) have progressed into transgenic animals. The B/B Homodimerizer (AP20187) has been the most widely used in vivo, and typically investigators have used doses of 0.5–10 mg per kg for each injection. At this dosage, 5 mg of dimerizer is sufficient for 20–400 injections for a 25-gram mouse. However, the exact dose and treatment must be determined empirically for each experiment.

Examples of in vivo mouse models for disease

  • The MaFIA mouse modelMacrophages are believed to play an important role in tumor development and progression. The Macrophage Fas-Induced Apoptosis (MaFIA) mouse is a widely adopted mouse model that allows for selective removal of macrophages through apoptosis (Burnett et al. 2004). The mechanism involves expression of a fas-DmrB fusion protein from a myeloid-specific promoter and its induced trimerization with the B/B Homodimerizer (AP20187). Trimerization of the fas death domain activates the caspase 8 pathway and leads to macrophage ablation in MaFIA mice.
  • Studying the roles of FGF receptor subtypes in prostate cancerProstate-specific expression of inducible versions of two subtypes of fibroblast growth factor receptor, FGFR-1 and FGFR-2, showed that only FGFR-1-induced neoplasia/hyperplasia in the prostate—implying its role in early prostate cancer development (Freeman et al. 2003). This mouse model can be used to test drug candidates that block the effects of FGFR1 dimerization.
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