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- 文献和实验
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4°C, protect from light
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货期:1-2天
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MedChemExpress LLC
- 规格:
10 mM * 1 mL/1 mg/5 mg/10 mg/25 mg
| 规格: | 10 mM * 1 mL | 产品价格: | ¥1655.0 |
|---|---|---|---|
| 规格: | 1 mg | 产品价格: | ¥681.0 |
| 规格: | 5 mg | 产品价格: | ¥1500.0 |
| 规格: | 10 mg | 产品价格: | ¥2500.0 |
| 规格: | 25 mg | 产品价格: | ¥5500.0 |
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GSK321
CAS No. : 1816331-63-1
MCE 国际站:GSK321
产品活性:GSK321 是突变异柠檬酸脱氢酶 1 (IDH1) 酶的有效抑制剂。GSK321 对突变的 IDH1 酶具有高抑制性和选择性。GSK321 可用于急性髓性白血病的研究。
研究领域:Metabolic Enzyme/Protease
作用靶点:Isocitrate Dehydrogenase (IDH)
In Vitro: GSK321 has high inhibitory for mutant IDH1 enzymes, with IC50 values of 4.6 nM against R132H, 3.8 nM against R132C and 2.9 nM against R132G, respectively.
GSK321 (0, 0.5, 5 μM; 48 h) induces markedly decreased H3K9me2 levels.
GSK321 decreases intracellular 2-HG and affects proliferation of primary IDH1 mutant AML cells.
GSK321 has inhibition activity for mutant IDH1 that overcomes the pathognomonic differentiation block of AML cells, and induces myeloid differentiation of IDH1 mutant cells at the level of leukemic blasts and more stem-like cells.
GSK321 leads to genome-wide DNA cytosine hypomethylation in IDH1-mutant AML cells.
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文献和实验0.0005 1 1.000 3.078 6.314 12.706 31.821 63.657 127.321 318.309 636.619 2 0.816 1.886 2.920 4.303 6.965 9.925 14.089 22.327 31.599 3 0.765 1.638 2.353 3.182 4.541 5.841 7.453 10.215 12.924 4 0.741 1.533 2.132 2.776 3.747 4.604
; Input稀释倍数(从1000ul体积中取了80ul作为input),对照样本(S1):其Ct值,Input为25.63; 目标蛋白31.935; 阴性对照33.14; Input稀释倍数(从1000ul体积中取了80ul作为input)。双△CT法:1. 标准化DNA的量 Normalize DNA.ΔCt [normalized ChIP] = (Ct [ChIP] - (Ct [Input] -Log2 (Input Dilution Factor)))Input Dilution Factor
) +(Nx * Wx)+( Ni* Wi) +16* Ns– 62. NA, NG, NC, NT, Ni分别为引物中碱基A或G或C或T或I的数量,WA, WC, WG, W, Wi分别为引物中碱基A或G或C或T或I的分子量,Nmod,Wmod 分别为修饰基团的数目和分子量。 对于混合碱基的分子量为混合碱基的分子量总合除以混合数,例如G+A混合的分子量为(313.21+329.21)/2 = 321.21。Ns为硫代数目,硫代每个位置增加分子量16。 常规碱基分子
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