| CAS: | 1139889-93-2 | ||
| 分子式: | C17H14F2N2 | ||
| 分子量: | 284.3 | ||
| 英文名称: |
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| 用途: | Golgicide A是一种有效的,快速可逆的GBF1抑制剂。Golgicide A抑制志贺毒素对蛋白质合成的作用,IC50 为3.3 μM。Golgicide A引起GBF1介导的Arf1活化减少,阻断可溶性分泌物和膜锚定蛋白,随后损害退化的毒素转运。[1] 在J6/JFH1细胞中,Golgicide A引起NS5A重新分配和传染性病毒颗粒的积累。[2] |
| 货号 | 品牌 | 产品名称 | 规格 | 包装、参考价格 | |||||||||||||||||||||||||||||||||
| G794045 | MACKLIN | Golgicide A | 10mM in DMSO | 648元/1ml; | 咨询 | ||||||||||||||||||||||||||||||||
储存:-20°C | |||||||||||||||||||||||||||||||||||||
| G872846 | MACKLIN | Golgicide A | 99% | 143元/5mg; 491元/25mg; 1421元/100mg; | 咨询 | ||||||||||||||||||||||||||||||||
储存:-20℃ 状态:粉末 | |||||||||||||||||||||||||||||||||||||
| 345862 | Sigma-Aldrich | Golgicide A-CAS 1139889-93-2-Calbiochem | A cell-permeable quinoline compound that selectively targets ArfGEF GBF1, but not BIG1/2, and attenuates GBF1-mediated cellular vesicle traffickings in a reversible manner. | 1954.93元/10 MG; | 咨询 | ||||||||||||||||||||||||||||||||
产品说明 一般描述 A cell-permeable quinoline compound that selectively targets ArfGEF GBF1, but not BIG1/2, and attenuates GBF1-mediated cellular vesicle traffickings in a reversible manner. Phenotypic comparisons in Vero (African Green Monkey Kidney epithelial) cultures reveal that selective blockage of GBF1 function by GCA (10 µM) or by FGB1-E794K dominant-inactive expression affects medial- and cis-Golgi similarly to that seen with BFA (Cat. No. 203729), however, the non-GBF1-specific BFA (10 µg/ml or 35.6 µM) causes additional GBF1-independent morphologic effects on TGN, notably the rapid dispersal of Golgi-associated coat proteins AP-1 and GGA3, which are not seen with GCA treatment. Endocytic/retrograde transport studies using GCA establishes that GBF1 function is not required for the transport of bacterial toxins to the endosomes, however the retrograde transport of StxB (shiga toxin B subunit) from endosomes to TGN and Golgi is GBF1-dependent (100% inhibition of StxB sulfation at 10 µM), accounting for GCA′s (10 µM) ability to completely prevent Vera cells from Stx-induced (up to 100 ng/ml) inhibition of cellular protein synthesis. 包装 10 mg in Plastic ampoule 警告 Toxicity: Standard Handling (A) 重悬 Following reconstitution, aliquot and freeze (-20°C). Stock solutions are stable for up to 6 months at -20°C. 其他说明 Saenz, J.B., et al. 2009. Nat. Chem. Biol.5, 157. 法律信息 CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany 基本信息
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