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RNase footprinting

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posted on 2011-12-30, 16:12 authored by Devanathan Raghunathan, Víctor M. Sánchez-Pedregal, Jochen Junker, Claudia Schwiegk, Markus Kalesse, Andreas Kirschning, Teresa Carlomagno

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Taken from "TAR-RNA recognition by a novel cyclic aminoglycoside analogue"

Nucleic Acids Research 2006;34(12):3599-3608.

Published online 19 Jul 2006

PMCID:PMC1524922.

© 2006 The Author(s)

RNase protection assays of the TAR/ complex were carried out with 10 µM 5′-P-labeled HIV-2 TAR-RNA at 4°C. The digestion experiments were analyzed by gel electrophoresis. () Digestion with RNase A (selective for C and U). Lane 1, control without RNase; lane 2, compound (10 mM); lane 3, compound (5 mM); lane 4, compound (500 µM); lane 5, compound (1.2 µM); lane 6, compound (0.12 µM). () Digestion with RNase T1 (G selective). Lane 1, control without RNase; lane 2, compound (10 mM); lane 3, compound (5 mM); lane 4, compound (500 µM); lane 5, compound (1.2 µM); lane 6, compound (0.12 µM).

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