Skip Navigation


Journal of Heredity Advance Access originally published online on October 7, 2008
Journal of Heredity 2009 100(2):246-250; doi:10.1093/jhered/esn083
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
100/2/246    most recent
esn083v1
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrowRequest Permissions
Google Scholar
Right arrow Articles by Triant, D. A.
Right arrow Articles by Whitehead, A.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Triant, D. A.
Right arrow Articles by Whitehead, A.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

© The American Genetic Association. 2008. All rights reserved. For permissions, please email: journals.permissions@oxfordjournals.org.

Brief Communications

Simultaneous Extraction of High-Quality RNA and DNA from Small Tissue Samples

Deborah A. Triant, and Andrew Whitehead

From the Department of Biological Sciences, Louisiana State University, Baton Rouge, LA 70803

Address correspondence to A. Whitehead at the address above, or e-mail: andreww{at}lsu.edu.

Purification of high-quality DNA and RNA from a single sample is becoming increasingly important for studies seeking both genomic and transcriptomic data. We compare different methods for isolating DNA and RNA from fish embryos (Gulf killifish; Fundulus grandis) and describe an optimal technique to extract high-quality DNA and RNA from a single embryo. The optimal method utilizes a chaotropic buffer and spin column technology. From embryos weighing ~4 mg, we were able to isolate an average of 6.1 µg of DNA and 1.1 µg of RNA per sample. Relative amounts of DNA and RNA can be adjusted as needed per study. Although these extraction trials were conducted on fish embryos, they can be potentially applied to small samples that typically do not yield high concentrations of nucleic acids.

Key Words: fish embryofundulusmicroarraynucleic acidTRIzol


Corresponding Editor: Jose Lopez

Received June 10, 2008
Revised August 13, 2008
Accepted September 5, 2008


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?




Disclaimer: Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.