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- 详细信息
- 文献和实验
- 技术资料
- 保存条件:
零下80~20°C
- 保质期:
Powder: -20°C for 3 years In solvent: -80°C for 2 years
- 英文名:
FLT3/ITD-IN-3
- 库存:
10
- 供应商:
TargetMol
- CAS号:
2489446-47-9
- 规格:
100 mg/25 mg/50 mg
| 规格: | 100 mg | 产品价格: | ¥17500.0 |
|---|---|---|---|
| 规格: | 25 mg | 产品价格: | ¥10600.0 |
| 规格: | 50 mg | 产品价格: | ¥13800.0 |
Product Introduction
Bioactivity
英文名:FLT3/ITD-IN-3
描述:FLT3/ITD-IN-3 (Compound 19) is a potent inhibitor of FLT3-ITD, acting on FLT3D835Y (IC50: 0.3 nM), FLT3 (IC50: 0.4 nM) and FLT3-ITD (IC50: 0.9 nM). FLT3/ITD-IN-3 showed potent inhibition of FLT3 phosphorylation and was effective against the proliferation of AML cells.

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文献和实验FLT3 Mutations in Acute Myeloid Leukemia
The prevalence of an internal tandem duplication (ITD) of the juxtamembrane domain-coding sequence and a missense mutation of D835 within the kinase domain of the FLT3 gene is 15–35% and 5–10% of adults with acute myeloid leukemia (AML
。 接下来,研究人员在58个AEL病人中(29个N-AEL,9个AML-MRC,13个MDS-AEL,7个普通AEL)进行了GATA2,CEBPA,NPM1和FLT3-ITD的18个突变的Sanger测序验证。结果显示,有42个病人中有17个携带一个突变,25个携带2个突变,6个携带3个突变,3个携带4个突变。其中,CEBPA突变频率为32.7%,GATA2突变频率为22.4%,NPM1突变频率为15.5%,SETBP1突变频率为12.1%,U2AF1突变频率为12.1%。值得注意的是,在AML发现
Gene Therapy of X-Linked Severe Combined Immunodeficiency
This review describes the main steps which led to carrying out the gene ther-apy clinical trial for Xlinked severe combined immune deficiency (SCID-X1) patients, from the preparation of the retroviral vector up to the design of GMP conditions
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