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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:
2471982-20-2
- 规格:
10 mM * 1 mL/1 mg/5 mg/10 mg/25 mg
| 规格: | 10 mM * 1 mL | 产品价格: | ¥2254.0 |
|---|---|---|---|
| 规格: | 1 mg | 产品价格: | ¥684.0 |
| 规格: | 5 mg | 产品价格: | ¥1800.0 |
| 规格: | 10 mg | 产品价格: | ¥2900.0 |
| 规格: | 25 mg | 产品价格: | ¥5000.0 |
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CU-115
CAS No. : 2471982-20-2
MCE 国际站:CU-115
产品活性:CU-115 是一种强有力的 TLR8 拮抗剂 (IC50=1.04 µM),并显示了对 TLR8 选择性高于TLR7 (IC50=>50 µM)。CU-115 降低了由 R-848 激活的 THP-1 细胞 TNF-α 和 IL-1β 的产生。
作用靶点:Toll-like Receptor (TLR)
In Vitro: In endosomal and non-endosomal TLR specificity studies, Human embryonic kidney (HEK) 293 cells expressing human tolllike receptor (hTLR) gene and an inducible secreted embryonic alkaline phosphatase (SEAP) reporter gene were incubated with CU-115 for 16 hours. As a result, CU-115 displays activity for TLR7 and TLR8 at low concentrations (0.5 μM).
CU-115 does not modulate the NF-kB inhibition induced by Pam2CSK4, Pam3CSK4, Poly(I:C), LPS, R848, and Flic in HEK-293 TLR1/2, TLR2/6, TLR3, and TLR4 cells. And CU-115 inhibits TLR9 signaling at 1, 5, and 20 µM and ~10-25% inhibition.
CU-115 (5-20 µM) inhibits increases in type I IFN transcriptional activity induced by the ssRNA nucleic acid ligands 3p-hpRNA or G3-YSD in a luciferase reporter assay.
CU-115 (0.5, 1.0, 5, and 20 µM; 16 hours) is nontoxic at low concentrations (0.5 and 20 μM) and toxic at 100 μM in Hek293 TLR7 and TLR8 cells. CU-115 also is nontoxic at low concentrations (0.5 and 20 μM) and displays partial toxicity at 100 μM in THP Dual cells.
The enzyme-linked immunosorbent assay (ELISA) is performed to measure upregulation/inhibition of TNF-α in human THP-1 cells (hTHP-1). CU-115 (5-20 µM) abolishes the TNF-α production activated by R848 (1 µg/ml) in hTHP1. It also represses the expression of IL-1β in hTHP-1 cells. These results suggest that CU-115 suppresses TLR8 and TLR7 signaling pathways.
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文献和实验强度为 32.15 万元/项。能够明显看出青年项目的数量最多,但面上项目获得的资助金额最高。这对于青年研究人员来说,挑战与机遇并存! 在各学科基金的激烈角逐征程中,细胞生物学方向受资助排名情况处于中上游,面上项目资助数 115 项,青年科学基金数目 101 项,地区科学基金项目 16 项,总体资助率在 17%-20% 之间。 根据国家自然科学基金委员会发布的 2024 年度项目指南,细胞生物学资助力度不容小觑,注意事项中明确提到资助的重点,包括细胞器及亚细胞结构、互作与功能等方面的研究。植物
主要特点:· 准确灵敏:BCA试剂的蛋白质测定范围是20-2000μg/ml,采用加强方法可检测到5μg/ml;MicroBCA试剂测定范围是0.5-20μg/ml。· 快速:45分钟内完成测定,比经典的Lowry法快4倍而且更加方便。· 经济实用:除试管外,测定可在微孔板中进行,大大节约样品和试剂用量。· 不受样品中离子型和非离子型去污剂影响。· 检测不同蛋白质分子的变异系数远小于考玛斯亮蓝。 基本原理: 碱性条件下,蛋白将Cu ++ 还原
:在碱性环境下蛋白质与Cu2+络合并将Cu2+还原成Cu1+(biuret reaction)。BCA与Cu1+结合形成稳定的紫蓝色复合物,在562 nM处有高的光吸收值并与蛋白质浓度成正比,据此可测定蛋白质浓度。 产品特点 1.步骤简单,45分钟内完成测定,比经典的Lowry法快4倍而且更加方便。 2.灵敏度高,检测浓度下限达到25μg/ml,最小检测蛋白量达到0.5μg,待测样品体积为1-20μl 。 3.BCA法测定蛋白浓度不受绝大部分样品中的去污
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