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- 详细信息
- 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:电询
- 供应商:
MedChemExpress LLC
- CAS号:
180977-44-0
- 规格:
10 mM * 1 mL/1 mg/5 mg/10 mg/25 mg/50 mg
| 规格: | 10 mM * 1 mL | 产品价格: | ¥1899.0 |
|---|---|---|---|
| 规格: | 1 mg | 产品价格: | ¥900.0 |
| 规格: | 5 mg | 产品价格: | ¥1800.0 |
| 规格: | 10 mg | 产品价格: | ¥2800.0 |
| 规格: | 25 mg | 产品价格: | ¥5500.0 |
| 规格: | 50 mg | 产品价格: | ¥7500.0 |
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GGTI298
CAS No. : 180977-44-0
MCE 国际站:GGTI298
产品活性:GGTI298 是有效的 GGTase I 抑制剂,能够抑制 geranylgeranylated Rap1A 的过程,对 farnesylated Ha-Ras 的过程也有一定影响,在体内,IC50 值分别为 3 和 > 20 μM。
研究领域:GPCR/G Protein | Apoptosis
In Vitro: Both RhoA inhibitor (GGTI298) and ROCK inhibitor (H1152) significantly reduce cAMP agonist-stimulated IK(ap), whereas the latter additionally reduces colocalization of KCNN4c with the apical membrane marker wheat germ agglutinin in T84WT cells.
Knockdown of DR4 abolishes NF-κB activation, leading to sensitization of DR5-dependent apoptosis induced by the combination of GGTI298 and TRAIL. GGTI298/TRAIL activates NF-κB and inhibits Akt. knockdown of DR5, preventes GGTI298/TRAIL-induced IκBα and p-Akt reduction, suggesting that DR5 mediates reduction of IκBα and p-Akt induced by GGTI298/TRAIL. In contrast, DR4 knockdown further facilitates GGTI298/TRAIL-induced p-Akt reduction.
In Vivo: The vivo mouse ileal loop experiments show fluid accumulation is reduced in a dose-dependent manner by TRAM-34, GGTI298, or H1152 when injected together with cholera toxin into the loop.
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文献和实验(see for example protocol #9). Forward primer The original primer pair used for the amplification of P2X2 are described in Brandle, U. et al.(1997). FEBS Letter 404, 294-298, and shown here for reference only.
煤炭通常指天然存在的泥煤、褐煤、烟煤和无烟煤以及人工产品木炭、焦炭、煤球等。煤的主要成分是碳、氢、氧三种元素,还有少量氮、硫、磷和一些稀有元素。煤中还含有泥、砂等矿物杂质和水分。碳(以石墨计)在298.15K时完全燃烧的热化学方程式为C(石墨) O 2 (g)=CO 2 (g);ΔH θ (298.15K)=-393.5kJ·mol-1对于1.000g碳(石墨)来说,ΔH θ (298.15K)=-32.8kJ·g -1 。但原煤中含有的氢,燃烧时与氧化合生成水
Use of Whole Embryo Culture for Studying Heart Development
, 2004; Dev Cell 14: 298–311, 2008). This technique is essentially growing a midgestation embryo ex utero in a test tube. One of the strengths of embryo culture is that it allows an investigator to easily manipulate or add drugs/chemicals
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