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NHEJ inhibitor-1
MCE 国际站:NHEJ inhibitor-1
产品活性:NHEJ inhibitor-1 (Compound C2) 是一种三功能 Pt(II) 复合物,可缓解非同源末端连接 (NHEJ)/同源重组 (HR) 相关的双链断裂 (DSB) 修复,从而避免非小细胞肺对顺铂的耐药性。NHEJ inhibitor-1 抑制损伤修复蛋白 Ku70 和 Rad51,从而使肿瘤对活性分子重新敏感。NHEJ inhibitor-1 还诱导 ROS 产生和 MMP 降低。
研究领域:Immunology/Inflammation | NF-κB | Metabolic Enzyme/Protease
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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
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文献和实验Mol Cell:杨薇等揭示 DNA-PK 的激活机制以及自磷酸化对 NHEJ 通路的重要作用
and Rad3-Related)三种激酶。 其中,DNA-PK 是非同源末端连接(Non-homologous end joining,NHEJ)通路中的关键蛋白激酶,由 DNA-PKcs(DNA-PK 催化亚基)、Ku70/80 和 DNA 末端组成,其全酶装配会进一步招募 NHEJ 相关的连接酶和修复蛋白,包括 DNA 连接酶 IV、XRCC4(X-ray cross complementing protein 4)、XLF(XRCC4-like factor)和 Artemis 等。 由于激酶
Similar to the trypsin inhibitor, the chymotrypsin inhibitor also decreases protein degradability in the intestine, resulting in lower availability of amino acids and peptides for production purposes. This adversely affects growth
city directed primarily toward trypsin (Kunitz inhibitor), and (2) those that have a molecular weight of only 6000 to 10,000 Da with a high proportion of cystine residues and are capable of inhibiting chymotrypsin as well as trypsin at independent
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