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- 文献和实验
- 技术资料
- 保存条件：
Powder: -20°C, 3 years; 4°C, 2 years. In solvent: -80°C, 6 months; -20°C, 1 month.
- 库存：
货期：1-2天
- 供应商：
MedChemExpress LLC
- CAS号：
425613-09-8
- 规格：
10 mM * 1 mL/5 mg/10 mg/25 mg/50 mg/100 mg
| 规格： | 10 mM * 1 mL | 产品价格： | ￥847.0 |
|---|---|---|---|
| 规格： | 5 mg | 产品价格： | ￥770.0 |
| 规格： | 10 mg | 产品价格： | ￥1320.0 |
| 规格： | 25 mg | 产品价格： | ￥2970.0 |
| 规格： | 50 mg | 产品价格： | ￥5170.0 |
| 规格： | 100 mg | 产品价格： | ￥9240.0 |
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SJ000291942
CAS No. : 425613-09-8
MCE 国际站：SJ000291942
产品活性：SJ000291942 是经典骨形态发生蛋白 (BMP) 信号传导途径的激活剂。BMP 是转化生长因子 β (TGFβ) 分泌信号分子家族的成员。
研究领域：TGF-beta/Smad
作用靶点：TGF-β Receptor
In Vitro: Embryos treated with SJ000291942 display the most severe ventralization and SJ000291942 is also the most potent. SJ000291942 also causes more mortality, and at lower doses than controls and the other two compounds. This demonstrates our compounds cause ventralization of embryos consistent with increased BMP signaling activity. SJ000291942 causes an increase in bmp2b and szl expression. Zebrafish assays suggest that SJ000291942 activates the canonical BMP signaling pathway. To extend these observations, immunoblotting of protein lysates from C33A-2D2 cells stimulated with SJ000291942 at different times is performed. SJ000291942 activates phosphorylation of SMAD1/5/8 in serum-free medium. Like in zebrafish embryos, SJ000291942 is most active. SJ000291942 induces p-SMAD1/5/8 maximally at 1hr of treatment. Immunoblotting analysis of lysates from C33A-2D2 treated with SJ000291942 reveals clear induction of the phosphorylated Extracellular Signal-regulated protein Kinase, ERK1/2 (P-ERK1/2) by SJ000291942. The highest dose (100 and 300ng) BMP4 treatments generate a gene expression signature most similar to osteoblast expression. Low dose (10ng) BMP4 treatment aligns closely with 25μM compound 3 treatment and with 25μM SJ000291942.
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文献和实验,Gregory B,Hover A,Chen MY,Luci J,Joo SJ,Handwerker D,Liang J,Boyd R,Hunicke- Smith S,Simpson ZB,Caven T, Sochat V,Shine JM,Gordon E,Snyder AZ,Adeyemo B,Petersen SE,Glahn D, McKay DR,Curran JE,Göring HHH,Carless MA,Blangero J,Frick L,Marcotte E, Mumford JA
RNAi相关文章（for free）Prospects of RNA interference therapy for cancerS I Pai, Y-Y Lin, B Macaes, A Meneshian, C-F Hung and T-C WuGene Ther 13: 464-477; advance online publication, December 8, 2005; doi:10.1038/sj.gt.3302694RNA interference in embryonic
of microdissected cells. References Debelenko LV, Brambilla E, Agarwal SK, Swalwell JI, Kester MB, Lubensky IA, Zhuang Z, Guru SC, Manickam P, Olufemi SE, Chandrasekharappa SC, Crabtree JS, Kim YS, Heppner C, Burns AL, Spiegel AM, Marx SJ, Liotta LA, Collins FS
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