4.8 Article

One-to-one quantum dot-labeled single long DNA probes

期刊

BIOMATERIALS
卷 32, 期 23, 页码 5471-5477

出版社

ELSEVIER SCI LTD
DOI: 10.1016/j.biomaterials.2011.04.013

关键词

Nanoparticle; DNA; PCR (polymerase chain reaction); In situ hybridization

资金

  1. NSFC [30870261, 20921062, 20875071]
  2. National genetically modified organism breeding major project [200908010-008B]
  3. Research Fund for the Doctoral Program of Higher Education [20090141110031]
  4. National Key Scientific Program (973)-Nanoscience and Nanotechnology [2011CB933600]

向作者/读者索取更多资源

Quantum dots (QDs) have been received most attention due to their unique properties. Constructing QDs conjugated with certain number of biomolecules is considered as one of the most important research goals in nanobiotechnology. In this study, we report polymerase chain reaction (PCR) amplification of primer oligonucleotides bound to QDs, termed as QD-based PCR. Characterization of QD-based PCR products by gel electrophoresis and atomic force microscopy showed that QD-labeled long DNA strands were synthesized and only a single long DNA strand was conjugated with a QD. The QD-based PCR products still kept fluorescence properties. Moreover, the one-to-one QD-labeled long DNA conjugates as probes could detect a single-copy gene on maize chromosomes by fluorescence in situ hybridization. Labeling a single QD to a single long DNA will make detection of small single-copy DNA fragments, quantitative detection and single molecule imaging come true by nanotechnology, and it will promote medical diagnosis and basic biological research as well as nano-material fabrication. (C) 2011 Elsevier Ltd. All rights reserved.

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