Advanced Search

Journal Navigation

Journal Home

Subscriptions

Archive

Contact Us

Table of Contents

Click here for more information

Sign In to gain access to subscriptions and/or personal tools.
Journal of Biomolecular Screening
This Article
Right arrow Full Text (PDF)
Right arrow References
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 Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to Saved Citations
Right arrow Download to citation manager
Right arrowRequest Permissions
Right arrow Request Reprints
Right arrow Add to My Marked Citations
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Web of Science (3)
Right arrow Citing Articles via Google Scholar
Right arrow Citing Articles via Scopus
Google Scholar
Right arrow Articles by Stump, M. D.
Right arrow Articles by Kamb, A.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Stump, M. D.
Right arrow Articles by Kamb, A.
Social Bookmarking
 Add to CiteULike   Add to Complore   Add to Connotea   Add to Del.icio.us   Add to Digg   Add to Reddit   Add to Technorati   Add to Twitter  
What's this?

An Automated System for Screening Retroviral Expression Constructs in Microplate Format

Mark D. Stump

Deltagen Proteomics, Inc. (Arcaris, Inc.) Salt Lake City, UT

Leonardo Di Sera

Deltagen Proteomics, Inc. (Arcaris, Inc.) Salt Lake City, UT

Matthew Rebentisch

Deltagen Proteomics, Inc. (Arcaris, Inc.) Salt Lake City, UT

Mark Endo

Deltagen Proteomics, Inc. (Arcaris, Inc.) Salt Lake City, UT

Michael Pierce

Deltagen Proteomics, Inc. (Arcaris, Inc.) Salt Lake City, UT

Alexander Kamb

Deltagen Proteomics, Inc. (Arcaris, Inc.) Salt Lake City, UT

Retroviruses are useful for genetics studies to deliver genes that express proteins, peptides, and RNAs. Several steps, including DNA preparation, transfection, packaging, transduction, and assay, are required to execute screens using retroviral constructs. Unlike screens with purified components, whole-cell assays using retroviral constructs need a large number of steps with microplate manipulations. The nature of these steps, especially the involvement of cultured mammalian cells, limits the throughput of such screens. To improve the efficiency of genetic experiments with retroviral expression vectors, an automated system for retroviral screening in microplates was devised and tested. The system, called Somata, provides high throughputs and robust, reproducible performance.

Journal of Biomolecular Screening, Vol. 7, No. 3, 275-280 (2002)
DOI: 10.1177/108705710200700311


Add to CiteULike CiteULike   Add to Complore Complore   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us   Add to Digg Digg   Add to Reddit Reddit   Add to Technorati Technorati   Add to Twitter Twitter    What's this?


This article has been cited by other articles:


Home page
J Biomol ScreenHome page
M. Pierce, C. Wang, M. Rebentisch, M. Endo, M. Stump, and A. Kamb
A High-Throughput, Homogeneous Microplate Assay for Agents That Kill Mammalian Tissue Culture Cells
J Biomol Screen, June 1, 2003; 8(3): 283 - 291.
[Abstract] [PDF]