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首页> 外文期刊>Talanta: The International Journal of Pure and Applied Analytical Chemistry >Chemiluminescence-imaging detection of DNA on a solid-phase membrane by using a peroxidase-labeled macromolecular probe
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Chemiluminescence-imaging detection of DNA on a solid-phase membrane by using a peroxidase-labeled macromolecular probe

机译:使用过氧化物酶标记的大分子探针对固相膜上的DNA进行化学发光成像检测

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摘要

We have developed a novel method for sensitive chemiluminescence (CL)-imaging detection of DNA by using a macromolecular probe synthesized by attaching multiple molecules of horseradish peroxidase (HRP) and biotin in dextran backbone. The probe formed a macromolecular assembly by binding to streptavidin which specifically recognized biotinylated complementary DNA, which was hybridized to a target DNA on a solid-phase membrane. This methodology was applied to CL-imaging detection of a synthetic telomere DNA (TTAGGG)(10) and human telomere DNA by using the CL probe comprising of dextranT2000 (MW=ca. 2000 kDa) bonded to approximately 42 molecules of HRP and 210 molecules of biotin. The human telomere DNA in a small number of buccal mucous cells (ca. 70 cell numbers) of cheek tissue was quantitatively determined by the proposed CL detection method that afforded approximately 10 times higher sensitivity than that of the conventional CL method using commercially available HRP-avidin probe. (C) 2015 Elsevier B.V. All rights reserved.
机译:我们已经开发了一种通过使用大分子探针合成DNA的化学发光(CL)成像检测的新方法,该探针是通过在右旋糖酐骨架上连接辣根过氧化物酶(HRP)和生物素的多个分子而合成的。该探针通过与链霉亲和素结合形成大分子组装体,该链霉亲和素特异性识别生物素化的互补DNA,该DNA与固相膜上的靶DNA杂交。通过使用包含与约42个HRP分子和210个分子结合的dextranT2000(MW = ca。2000 kDa)的CL探针,该方法被应用于合成端粒DNA(TTAGGG)(10)和人端粒DNA的CL成像检测。生物素。通过拟议的CL检测方法定量测定了脸颊组织的少量颊黏膜细胞(约70个细胞数)中的人类端粒DNA,该检测方法的灵敏度比使用市售HRP-抗生物素蛋白探针。 (C)2015 Elsevier B.V.保留所有权利。

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