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Enhance the binding affinity of fluorophore-aptamer pairs for RNA tagging with neomycin conjugation

Fluorogenic sulforhodamine-neomycin conjugates have been designed and synthesized for RNA tagging. Conjugates were fluorescently activated by binding to RNA aptamers and exhibited greater than 250–400 fold enhancement in binding affinity relative to corresponding unconjugtaed fluorophores.

Αποθηκεύτηκε σε:
Λεπτομέρειες βιβλιογραφικής εγγραφής
Κύριοι συγγραφείς: Jeon, Jongho, Lee, Kyung Hyun, Rao, Jianghong
Μορφή: Artigo
Γλώσσα:Inglês
Έκδοση: 2012
Θέματα:
Διαθέσιμο Online:https://ncbi.nlm.nih.gov/pmc/articles/PMC3728288/
https://ncbi.nlm.nih.gov/pubmed/22951899
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1039/c2cc34498j
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