万千商家帮你免费找货
0 人在求购买到急需产品
- 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:1-2天
- 供应商:
MedChemExpress LLC
- 规格:
10 mM * 1 mL/5 mg/10 mg/25 mg/50 mg/100 mg/250 mg
| 规格: | 10 mM * 1 mL | 产品价格: | ¥586.0 |
|---|---|---|---|
| 规格: | 5 mg | 产品价格: | ¥533.0 |
| 规格: | 10 mg | 产品价格: | ¥799.0 |
| 规格: | 25 mg | 产品价格: | ¥1319.0 |
| 规格: | 50 mg | 产品价格: | ¥1979.0 |
| 规格: | 100 mg | 产品价格: | ¥2968.0 |
| 规格: | 250 mg | 产品价格: | ¥5040.0 |
MCE 的所有产品仅用作科学研究或药证申报,我们不为任何个人用途提供产品和服务。
PROTAC BCR-ABL1 ligand 1
CAS No. : 2489876-34-6
MCE 国际站:PROTAC BCR-ABL1 ligand 1
产品活性:PROTAC BCR-ABL1 ligand 1,化合物 GMB-475, 是靶向蛋白水解的嵌合体 (PROTAC) 的配体,其以变构方式靶向 BCR-ABL1 蛋白并募集 E3 连接酶 Von Hippel-Lindau,从而导致泛素化和随后的 BCR-ABL1 蛋白的降解。
研究领域:Protein Tyrosine Kinase/RTK
作用靶点:Bcr-Abl
In Vitro: GMB-475 (0-10 μM) exhibits cell proferation with IC50 values of 1.11,1.98,0.37 μM for BCR-ABL1 WT, T315I, G250E cells, respectively.
GMB-475 (0-30 μM) induces the degradation of BCR-ABL1 and c-ABL1 with concomitant inhibition of downstream signaling via the STAT5 pathway, in a dose- and time-dependent fashion in the context of both K562 and Ba/F3 cells.
相关产品:Dasatinib | Nocodazole | Imatinib | Ponatinib | Nilotinib | Bosutinib | Asciminib | Degrasyn | Rebastinib | Olverembatinib | AT9283 | KW-2449 | LXH254 | Bafetinib | DPH | AST 487 | Flumatinib | PD173955 | Vodobatinib | BV02 | GNF-2 | XL228 | GNF-7 | Cenisertib | GNF-5
热门产品线:重组蛋白 | 化合物库 | 天然产物 | 荧光染料 | PROTAC | 同位素标记物
Trending products:Recombinant Proteins | Bioactive Screening Libraries | Natural Products | Dye Reagents | PROTAC | Isotope-Labeled Compounds
风险提示:丁香通仅作为第三方平台,为商家信息发布提供平台空间。用户咨询产品时请注意保护个人信息及财产安全,合理判断,谨慎选购商品,商家和用户对交易行为负责。对于医疗器械类产品,请先查证核实企业经营资质和医疗器械产品注册证情况。
文献和实验In Vitro Effects of Adjuvants on B Cells
Stimulation of B cells not only through the B cell antigen receptor (BCR) but also through Toll-like receptors (TLRs) can drive activation, proliferation, and differentiation of B cells to result in antigen-specific antibody secretion
Exploring Pathways from Gene Co-expression to Network Dynamics
BCR–ABL pathway. The examinations disclosed both linear and nonlinear relationships of ligand–receptor interactions associated with cancer development, identified disease and drug targets of leukemia, and provided new insights into biology
-L2的表达,可导致T细胞增殖和细胞因子(IFN-γ和IL-10)产生增加,且同时阻断二者表现的作用相加,表明PD-L1和PD-L2的功能是抑制T细胞活化[7]。PD-1也可参与B细胞应答的负调节。PD-1-/-小鼠可出现脾肿大、B细胞增殖、血清Ig增加,以及多种自身免疫症状,提示PD-1信号传导的作用是抑制B细胞增殖、分化、Ig类型转换,在建立和/或维持外周自身耐受中起重要作用[8-10]。PD-1抑制BCR介导的信号转导的分子机制是:PD-1通过其所含SH2区的酪氨酸磷酸酶2(SHP-2),使BCR
技术资料暂无技术资料 索取技术资料















