Awardee OrganizationSALK INSTITUTE FOR BIOLOGICAL STUDIES
Description
Abstract Text
PROJECT SUMMARY – VIRAL VECTOR
Utilization of recombinant viral vectors are the method of choice for targeted, rapid, and regulated gene delivery
in many experimental systems. Access to this technology allows Salk Cancer Center (SCC) scientists to control
genetic activity in cells or in whole animals with the goal of better understanding fundamental cellular functions
and the molecular underpinnings of cancer and other disease processed. The Viral Vector Shared Resource
(VVC) specializes in the design, development, and production of high quality in vitro- and in vivo-grade
recombinant viral vectors. It offers convenient ready-to-use stocks, as well as custom preparations of lentiviral
vectors, retroviral vectors, adenoviral vector, adeno-associated viral vectors (AAVs), vesicular stomatitis viral
vectors (VSVs), and rabies vectors. In addition to providing these vector stocks and custom production services,
the VVC also maintains a plasmid archive of all viral vectors that have been submitted to the Shared Resource.
The plasmid library of packaging plasmids and transfer plasmids for our stock vectors is available at no cost to
SCC investigators as a resource for cloning purposes or for packaging viral vector constructs in their own. The
VVC is used by 35% of SCC members (11) who are responsible for 62% of all Salk utilization based on
recharges. The VVC is located a short walk from the Salk Institute in the Sanford Consortium for Regenerative
Medicine building (SCRM). Relocation of the VVC to SCRM, along with subsidized rates for Cancer Center
members, were designed to promote shared resource usage and collaborations among the C3 member
institutions on the mesa (see Overall: Transdisciplinary Collaboration for C3 description).
No Sub Projects information available for 5P30CA014195-52 7645
Publications
Publications are associated with projects, but cannot be identified with any particular year of the project or fiscal year of funding. This is due to the continuous and cumulative nature of knowledge generation across the life of a project and the sometimes long and variable publishing timeline. Similarly, for multi-component projects, publications are associated with the parent core project and not with individual sub-projects.
No Publications available for 5P30CA014195-52 7645
Patents
No Patents information available for 5P30CA014195-52 7645
Outcomes
The Project Outcomes shown here are displayed verbatim as submitted by the Principal Investigator (PI) for this award. Any opinions, findings, and conclusions or recommendations expressed are those of the PI and do not necessarily reflect the views of the National Institutes of Health. NIH has not endorsed the content below.
No Outcomes available for 5P30CA014195-52 7645
Clinical Studies
No Clinical Studies information available for 5P30CA014195-52 7645
News and More
Related News Releases
No news release information available for 5P30CA014195-52 7645
History
No Historical information available for 5P30CA014195-52 7645
Similar Projects
No Similar Projects information available for 5P30CA014195-52 7645