Fig. 7.
Fig. 7. Transgene activity in an animal model of gram-negative sepsis. LPS was administered to mice (colony 32) containing a luciferase transgene under the control of the mouse GP Ibα promoter. The wide range of LPS-induced effects and toxicity in mice is well documented and doses administered to individual mice were sufficient to achieve maximal levels for a variety of cytokines. LPS was administered by intraperitoneal injection (25 mg/kg) and luciferase activity in the major murine organs was determined. Results are shown for assays performed 24 hours postinjection, although similar results were obtained at 4-hour intervals leading up to the 24-hour assay shown. The mean and standard error of the mean are shown for each organ (n = 4). Control mice were injected intraperitoneally with an equal volume of saline buffer. No differences in the levels of luciferase activity were observed at any time point.

Transgene activity in an animal model of gram-negative sepsis. LPS was administered to mice (colony 32) containing a luciferase transgene under the control of the mouse GP Ibα promoter. The wide range of LPS-induced effects and toxicity in mice is well documented and doses administered to individual mice were sufficient to achieve maximal levels for a variety of cytokines. LPS was administered by intraperitoneal injection (25 mg/kg) and luciferase activity in the major murine organs was determined. Results are shown for assays performed 24 hours postinjection, although similar results were obtained at 4-hour intervals leading up to the 24-hour assay shown. The mean and standard error of the mean are shown for each organ (n = 4). Control mice were injected intraperitoneally with an equal volume of saline buffer. No differences in the levels of luciferase activity were observed at any time point.

Close Modal

or Create an Account

Close Modal
Close Modal