z-logo
open-access-imgOpen Access
Use of Fluorescent Microspheres to Localize In Vivo Gene Transfer Injection Sites
Author(s) -
Michael A. Flynn,
Yoram Vodovotz,
Ran Kornowski,
Stephen E. Epstein,
David Gordon,
J.A. Keiser
Publication year - 2000
Publication title -
biotechniques
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.617
H-Index - 131
eISSN - 1940-9818
pISSN - 0736-6205
DOI - 10.2144/00283st04
Subject(s) - transfection , in vivo , genetic enhancement , green fluorescent protein , gene delivery , gene , gene expression , microbiology and biotechnology , gene product , gene transfer , fluorescence , biology , fluorescence microscope , chemistry , biochemistry , genetics , physics , quantum mechanics
The potential for using gene therapy to treat a variety of disease states is growing rapidly. Many vector types and delivery systems have been developed that allow the optimization of protein production levels and kinetics for a given therapeutic gene product. In cases in which a transient, localized delivery of gene product is desired, any determination of the locale of transfected tissue by non-marker genes is problematic. We describe a technique by which the use of fluorescent microspheres can help in identifying potentially transfected tissue. Adenovirus containing the gene for β-galactosidase (β-gal) was mixed with fluorescent microspheres and injected into rat skeletal muscle and porcine myocardium. The injection sites could be visualized under ultraviolet light and correlated with β-gal enzyme expression. This method is simple, inexpensive and generally useful for in vivo gene transfer experiments.

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom