-
Categories
-
Pharmaceutical Intermediates
-
Active Pharmaceutical Ingredients
-
Food Additives
- Industrial Coatings
- Agrochemicals
- Dyes and Pigments
- Surfactant
- Flavors and Fragrances
- Chemical Reagents
- Catalyst and Auxiliary
- Natural Products
- Inorganic Chemistry
-
Organic Chemistry
-
Biochemical Engineering
- Analytical Chemistry
-
Cosmetic Ingredient
- Water Treatment Chemical
-
Pharmaceutical Intermediates
Promotion
ECHEMI Mall
Wholesale
Weekly Price
Exhibition
News
-
Trade Service
The study of gene regulation has been greatly enhanced by the use of reporter gene systems such as beta galactosidase (P-gal), neomycin phosphotransferase (APH[3]11), chloramphenicol acetyl transferase (CAT), beta glucuronidase (GUS), and dihydrofolate reductase (DHFR). In the past several years, development of marker gene systems based on bioluminescence have extended the power of marker gene technology from enzymatic or color based in vitro assays to more sensitive single photon counting methods m vitro and in vivo A variety of proteins that catalyze bioluminescent reactions have been isolated and characterized. For several of these proteins, the genes are available and are currently being used as reporters for gene expression studies. Concomttant advances m single photon detection technology have recently made tt possible to measure gene expression nonmvasively m real time. We describe here the apphcatton of bacterial luciferase from
Vibrio hawey
i and eukaryotic luctferase from
Renillurenifomzi
s as markers for transformation and reporters of gene expression m transgemc plants. The major advantages of the luciferase gene expression system are its simplicity, sensitivity, safety for the investtgator and available nondestructive assay conditions, which permit real-time measurements of gene expression continuously throughout development of transgenic plants.
