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- HY-P4917A
- 2026年01月25日
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- 库存：
50
- 供应商：
广州市左克生物
- CAS号：
//
- 规格：
1mg/5mg/10mg
| 规格： | 1mg | 产品价格： | ￥680.0 |
|---|---|---|---|
| 规格： | 5mg | 产品价格： | ￥1700.0 |
| 规格： | 10mg | 产品价格： | ￥2720.0 |
CAS号:
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文献和实验Assay of Mammalian Ornithine Decarboxylase Activity Using [14C]Ornithine
(2 ). It has been shown that mutation of cysteine 360 to alanine (C360A) results in an enzyme not only having greatly reduced activity, but the activity of this mutant is much more stable than wild-type ODC in the absence of dithiothreitol. The high dependence of ODC
Cyclooxygenase Inhibitors Induce Colon Cancer Cell Apoptosis Via PPAR 14-3-3 Pathway
activity and abrogating 14-3-3e upregulation. Furthermore, the COX-2 inhibitors suppress PPARδ expression. Suppression of PPARδ leads to reduced 14-3-3e and hence a decline in Bad sequestration, resulting in an increased Bad-induced apoptosis
can be selectively inhibited by targeting the catalytic site with drug?like compounds. Notably, the mammalian 26S proteasome is associated with three major DUBs: RPN11, UCH37, and USP14. Because the ubiquitin ?chain?trimming? activity of USP14 can inhibit proteasome
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