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- 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
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MedChemExpress LLC
- CAS号:
1798331-92-6
- 规格:
10 mM * 1 mL/5 mg/10 mg/50 mg/100 mg
| 规格: | 10 mM * 1 mL | 产品价格: | ¥990.0 |
|---|---|---|---|
| 规格: | 5 mg | 产品价格: | ¥900.0 |
| 规格: | 10 mg | 产品价格: | ¥1500.0 |
| 规格: | 50 mg | 产品价格: | ¥4500.0 |
| 规格: | 100 mg | 产品价格: | ¥8500.0 |
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QX77
CAS No. : 1798331-92-6
MCE 国际站:QX77
产品活性:QX77 是分子伴侣介导的自噬 (CMA) 激活剂,可上调 LAMP2A 的表达。QX77 诱导 Rab11 上调,挽救 Rab11 下调和转运缺陷。QX77 可抑制 ES 细胞自我更新,促进分化。
研究领域:Autophagy
作用靶点:Autophagy
In Vitro: QX77 (48 hours) upregulates Rab11 expression levels in Ctns-/- MEFs.
In Ctns-/- MEFs, QX77 recovers the down-regulated LAMP2A expression, and the Rab11-positive carrier vesicles recover the high-motility trafficking phenotype observe in wild-type cells.
Treatment with CMA activator QX77 rescues Rab11 down-regulation and trafficking deficiency in cystinotic cells. QX77 treatment also increases LAMP2A localization at the lysosomal membrane.
QX77 significantly increases the re-localization of LAMP2A at LAMP1-positive lysosomes in cystinotic cell, it corrects the localization of LAMP2A at the lysosomal membrane in cystinotic cells.
QX77 protects cystinotic cells from the increased susceptibility to tert-butyl-hydroperoxide-induced oxidative stress and reconstitutes the resistant levels observed in wild-type cells. The effect of QX77 on cystinotic cell survival is dependent on LAMP2A expression.
QX77 (10 μM; 0, 3 or 6 days) activates CMA and increases LAMP2A expression in D3 and E14 ES cell, it downregulates pluripotency factors and AP reactivity and partially lost the characteristic ES cell morphology.
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文献和实验CD77 分子 CD77 常用单克隆抗体或代号: 38.13(BL- A),424/4A11 主要表达细胞: Bac [B] 分子质量(kDa)和结构: Globotriaocylceramide(Gb3) 功 能: 参与凋亡过程中跨膜信号转导 CD77 Aka globotriaosylceraminde, pK blood group Binds to Shiga
实验77 苍耳的光周期诱导 原理 植物在发育地程中需要有一定的光周期诱导才能进入性器官的分化,从而达到开花结实。苍耳是短日照植物,短的光周期诱导能促使其性器官分化,提早开花结实。 仪器 供短日处理的暗箱或暗室 小花盆 光照自控装置 双筒解剖镜 操作步骤 1.将苍耳种子播种
Genotype 1a HCV (H77S) Infection System
research, the parallel development of a tractable genotype 1a infection system (H77S virus) has provided significant advantages in assessing genotype 1-specific interventions, given the highly heterogeneous nature of HCV. H77S RNA contains five cell culture
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