Literature DB >> 19232314

Gel purification of radiolabeled nucleic acids via phosphorimaging: Dip-N-Dot.

Aaron S Burton1, Rowan A Madix, Nilesh Vaidya, Craig A Riley, Eric J Hayden, Andre Chepetan, Carolina Díaz Arenas, Brian C Larson, Niles Lehman.   

Abstract

RNA and DNA oligonucleotides radiolabeled with (32)P or (33)P often require gel electrophoresis to remove undesired side and/or degradation products. Common ways to visualize these molecules after electrophoresis are by ultraviolet (UV) shadowing, which necessarily reduces the specific activity of the oligonucleotide, and by autoradiography using film, which is cumbersome and increases the cost of generating the radiolabeled molecule. A more cost-effective method is to physically inject the gel with a "Dip-N-Dot" solution of dye and radionuclide after electrophoresis but prior to phosphorimaging. The gel can be overlaid on its computer-generated image, allowing the labeled molecules to be visualized quickly.

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Year:  2009        PMID: 19232314     DOI: 10.1016/j.ab.2009.02.010

Source DB:  PubMed          Journal:  Anal Biochem        ISSN: 0003-2697            Impact factor:   3.365


  3 in total

1.  Enhancing the prebiotic relevance of a set of covalently self-assembling, autorecombining RNAs through in vitro selection.

Authors:  Aaron S Burton; Niles Lehman
Journal:  J Mol Evol       Date:  2010-03-03       Impact factor: 2.395

2.  Partitioning the fitness components of RNA populations evolving in vitro.

Authors:  Carolina Díaz Arenas; Niles Lehman
Journal:  PLoS One       Date:  2013-12-31       Impact factor: 3.240

3.  One RNA plays three roles to provide catalytic activity to a group I intron lacking an endogenous internal guide sequence.

Authors:  Nilesh Vaidya; Niles Lehman
Journal:  Nucleic Acids Res       Date:  2009-04-30       Impact factor: 16.971

  3 in total

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