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首页> 外文期刊>Spectrochimica acta, Part A. Molecular and biomolecular spectroscopy >Detection of the level of DNMT1 based on self-assembled probe signal amplification technique in plasma
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Detection of the level of DNMT1 based on self-assembled probe signal amplification technique in plasma

机译:基于自组装探针信号放大技术检测等离子体中的DNMT1水平

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DNA (cytosine-5)-methyltransferase1 (DNMT1) is the most abundant DNA methyltransferase in somatic cells, and it plays an important role in the initiation, occurrence, and rehabilitation of tumors. Herein, we developed a novel strategy for the detection of the level of DNMT1 in human plasma using the selfassembled nucleic acid probe signal amplification technology. In this method, the DNMT1 monoclonal antibody (McAbDNMT1) was immobilized on carboxyl magnetic beads to form immunomagnetic beads and then captured DNMT1 specifically. After that, DNMT1 polyclonal antibody (PcAbDNMT1) and biotinylated sheep anti-rabbit IgG (sheep anti rabbit IgG-Biotin) were sequentially added into the system to react with DNMT1 and form biotinylated double antibody sandwich immunomagnetic beads. In the presence of the bridging medium streptavidin, the biotinylated double antibody sandwich immunomagnetic beads would form a complex with biotinylated poly-fluorescein (Biotin-poly FAM), and the fluorescence intensity of the complex was proportional to the concentration of DNMT1. Immunomagnetic beads can capture the target DNMT1 in the sample, and Biotin-poly FAM can realize signal amplification. Using these strategies, we got a linear range of the system for DNMT1 level detection was from 2 nmol/L to 200 nmol/L, and the limit of detection (LOD) was 0.05 nmol/L. The method was successfully applied for the determination of DNMT1 in human plasma with the recovery of 101.3-106.0%. Therefore, this method has the potential for the detection of DNMT1 level in clinical diagnosis. @2021 Elsevier B.V. All rights reserved.
机译:DNA(胞嘧啶-5)-甲基转移酶1(DNMT1)是体细胞中含量最丰富的DNA甲基转移酶,在肿瘤的发生、发生和修复中起着重要作用。在此,我们开发了一种利用自组装核酸探针信号放大技术检测人血浆中DNMT1水平的新策略。在该方法中,DNMT1单克隆抗体(McAbDNMT1)被固定在羧基磁珠上形成免疫磁珠,然后特异性捕获DNMT1。随后,将DNMT1多克隆抗体(PcAbDNMT1)和生物素化绵羊抗兔IgG(绵羊抗兔IgG生物素)依次加入到系统中,与DNMT1反应,形成生物素化双抗体夹心免疫磁珠。在架桥介质链霉亲和素存在下,生物素化双抗体夹心免疫磁珠将与生物素化聚荧光素(生物素-聚FAM)形成复合物,该复合物的荧光强度与DNMT1的浓度成正比。免疫磁珠可以捕获样本中的目标DNMT1,生物素聚FAM可以实现信号放大。利用这些策略,我们得到了DNMT1水平检测系统的线性范围为2 nmol/L至200 nmol/L,检测限(LOD)为0.05 nmol/L。该方法成功地应用于人血浆中DNMT1的测定,回收率为101.3-106.0%。因此,该方法有可能在临床诊断中检测DNMT1水平@2021爱思唯尔B.V.保留所有权利。

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