The mouse genome can be made to express a variety of reporter genes.

The expression distribution of the reporter gene can be determined by visualizing it.

If the two proteins do not interact, there is no transcription of the reporter gene.

The following sections outline in brief some of the reporter gene systems available and their existing applications.

Luciferase systems are widely used in the field of genetic engineering as reporter genes.

Both the mouse and human p27 Kip1promoter regions have previously been characterized using reporter gene constructs.

Schematic representations of the fusion proteins and reporter gene that were used.

Sensitivity may also be controlled by varying the dependency of the cells on their reporter genes.

The reporter gene is necessary for identification of the spatial regulation by enhancers.

They then linked their reporter gene to a promoter that was bound by the repressor.

Research highlights and updated information on reporter genes.

A scientist knows that a new gene has been trapped when the reporter gene is expressed.

Other fusion proteins such as green fluorescent protein may act as a reporter gene.

Reporter genes can be used to assay for the activity of a particular promoter in a cell or organism.

This structured element increases translation of the apoB protein or a reporter gene.

The reporter gene would then serve as a marker of when the chromatin became 'open' to regulatory and transcription factors.

Look for flies expressing the reporter gene.

This luminescence has been a useful device in the study of plant chloroplast function and as a reporter gene.

In the case of a bioreporter, these genes, or portions thereof, have been removed and replaced with a reporter gene.

The isolated survivin promoter was placed upstream of the luciferase reporter gene.

If this specific promoter region is also attached to a reporter gene, we can see when the transactivator is being expressed.

Random transposition occurs, inserting the gene of interest and reporter gene.

Screen plasmids for the E. coli reporter gene.

A selectable marker is a reporter gene introduced into a cell along with a gene insert.

Clearly, only direct experimental validation of predicted modules through reporter gene fusions will help to compare the different methods.