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2982527-11-5
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询盘
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HIV-1 protease-IN-10
MCE 国际站:HIV-1 protease-IN-10
产品活性:HIV-1 protease-IN-10 (Compound 2) 具有 HIV-1 潜伏期逆转活性 (IC50: 0.22 μM)。HIV-1 protease-IN-10 与 PKCδ C1b 结构域结合 (IC50: 0.69 μM)。HIV-1 protease-IN-10 对酯酶介导的水解具有稳定性。
研究领域:Anti-infection | TGF-beta/Smad | Epigenetics
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文献和实验liufengxi HIV-1 Tat (47-57) N-term Cys 序列 H-CYGRKKRRQRRR-NH2 ;原始HIV-1 Tat (47-57)序列为YGRKKRRQRRR 。N端的半胱氨酸修饰是为了利用其含有的巯基和其他分子反应,但是C端得-NH2的修饰是什么目的呢?有这个修饰的必要吗?是为了增强多肽的活性,还是发挥一个阻断活性COOH的作用? 附件是关于HIV-1 Tat (47-57) N-term Cys的产品介绍。请高手
A Conformationally Restricted -Strand HIV Protease Inhibitor
after the potent HIV protease inhibitor 2 , which together with a series of related derivatives was developed at Abbott Laboratories ( 11 ). This pseudopeptide contains a symmetrical diamino diol motif 8 (Fig. 2 ) flanked by Cbz-protected valine residues
Detection of HIV-1 Nucleic Acids by Northern Blotting
cells, blood, and tissue. For HIV research, Northern blotting has been utilized for determining the expression levels and splicing patterns of HIV RNA regulatory genes (2 –4 ), HIV RNA protease gene (5 ), cytokine effects on the levels of spliced
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