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Homogeneous point mutation detection by quantum dot-mediated two-color fluorescence coincidence analysis

This report describes a new genotyping method capable of detecting low-abundant point mutations in a homogeneous, separation-free format. The method is based on integration of oligonucleotide ligation with a semiconductor quantum dot (QD)-mediated two-color fluorescence coincidence detection scheme....

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Bibliografiska uppgifter
Huvudupphovsmän: Yeh, Hsin-Chih, Ho, Yi-Ping, Shih, Ie-Ming, Wang, Tza-Huei
Materialtyp: Artigo
Språk:Inglês
Publicerad: Oxford University Press 2006
Ämnen:
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC1390686/
https://ncbi.nlm.nih.gov/pubmed/16517937
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/nar/gkl021
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