Skip Navigation

This Article
Right arrow Full Text Freely available
Right arrow Print PDF (120K) Freely available
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 ISI Web of Science
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 arrow Search for citing articles in:
ISI Web of Science (17)
Right arrowRequest Permissions
Right arrow Commercial Re-use Guidelines
for Open Access NAR Content
Google Scholar
Right arrow Articles by Erfle, H.
Right arrow Articles by Ansorge, W.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Erfle, H.
Right arrow Articles by Ansorge, W.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Nucleic Acids Research, Vol 25, Issue 11 2229-2230, Copyright © 1997 by Oxford University Press


ARTICLES

Simultaneous loading of 200 sample lanes for DNA sequencing on vertical and horizontal, standard and ultrathin gels

H Erfle, R Ventzki, H Voss, S Rechmann, V Benes, J Stegemann and W Ansorge
Biochemical Instrumentation, EMBL Heidelberg, Meyerhofstrasse 1, 69117 Heidelberg, Germany.

We have developed a simple and efficient technique for automated parallel loading of >/=200 lanes on a 30 cm-wide gel in automated DNA sequencing, using porous filter materials and an associated manual or robotic system. The samples are loaded onto the teeth of a comb made of the porous material. The comb, with samples, is inserted directly above the straight edge of the polymerized gel. The samples are driven from the comb into the gel by the applied electrical field. A particularly advantageous aspect of this method is the elimination of the thin gel walls separating the sample wells in the standard gel loading technique. The time for sample loading is significantly reduced to a few minutes. The loading technique is applicable to horizontal or vertical systems, with standard or ultrathin gels.
Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
J. Biol. Chem.Home page
T. R. Pacheco, A. Q. Gomes, N. L. Barbosa-Morais, V. Benes, W. Ansorge, M. Wollerton, C. W. Smith, J. Valcarcel, and M. Carmo-Fonseca
Diversity of Vertebrate Splicing Factor U2AF35: IDENTIFICATION OF ALTERNATIVELY SPLICED U2AF1 mRNAs
J. Biol. Chem., June 25, 2004; 279(26): 27039 - 27049.
[Abstract] [Full Text] [PDF]


Home page
Genome ResHome page
P. V. Benos, M. K. Gatt, L. Murphy, D. Harris, B. Barrell, C. Ferraz, S. Vidal, C. Brun, J. Demaille, E. Cadieu, et al.
From First Base: The Sequence of the Tip of the X Chromosome of Drosophila melanogaster, a Comparison of Two Sequencing Strategies
Genome Res., May 1, 2001; 11(5): 710 - 730.
[Abstract] [Full Text]


Home page
Genome ResHome page
D. Meldrum
Automation for Genomics, Part Two: Sequencers, Microarrays, and Future Trends
Genome Res., September 1, 2000; 10(9): 1288 - 1303.
[Abstract] [Full Text]


Home page
Mol. Biol. CellHome page
A. J. Kal, A. J. van Zonneveld, V. Benes, M. van den Berg, M. G. Koerkamp, K. Albermann, N. Strack, J. M. Ruijter, A. Richter, B. Dujon, et al.
Dynamics of Gene Expression Revealed by Comparison of Serial Analysis of Gene Expression Transcript Profiles from Yeast Grown on Two Different Carbon Sources
Mol. Biol. Cell, June 1, 1999; 10(6): 1859 - 1872.
[Abstract] [Full Text]


Home page
Genome ResHome page
D. A. Panussis, M. W. Cook, L. L. Rifkin, J. E. Snider, J. T. Strong, R. M. McGrane, R. K. Wilson, and E. R. Mardis
A Pneumatic Device for Rapid Loading of DNA Sequencing Gels
Genome Res., May 1, 1998; 8(5): 543 - 548.
[Abstract] [Full Text]



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.