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Aldevron provides bulk quantities of eukaryotic
reporter plasmids. Plasmids encoding luciferase, GFP, betagalactosidase,
SEAP, and CAT are available.
Ultra-Pure - Ready to Use
Genlantis Inc.,
has engineered a new series of reporter
plasmids based on the gWiz™ high-expression
vector system. These plasmids have
been designed to produce the highest levels of gene expression in a wide
range of mammalian cells and tissues. They contain a proprietarily modified
promoter followed by intron A from the CMV immediate early gene and a
high-efficiency artificial transcription terminator. The expression vectors
are constructed in a plasmid backbone which has been extensively modified
to achieve enhanced levels of transgene expression in
mammalian cells.
Milligram Amounts Available
Aldevron now offers ultra-pure, milligram
amounts of these plasmids for use by Gene Therapy and DNA Vaccine
researchers. Aldevron's exclusive fermentation technology and DNA
purification process are used to produce the gWiz™ High-Expression
Reporter Plasmids. The ready-to-use plasmids are endotoxin-free and
can be applied directly to most in vitro and in
vivo applications.
Plasmids can be delivered in the buffer of your choice for an additional
charge of $25. Material otherwise will ship in water. The turn-around
time is approximately 24 to 48 hours. Significant volume discounts
are available. Please inquire for further details.

Cell
types as indicated were transfected in 24-well plates with 1 ug of
the gWiz B-galactosidase vector or 1 ug of the CMV-1 or CMV-2 vectors
(commercial vectors with CMV IE promoter regulating the B-gal gene)
and 5 ul of GenePORTER transfection reagent. For Jurkat cells, 8 ul
of GenePORTER reagent was used. The graph for each transfection represents
the mean of two separate experiments in which each sample was tested
in duplicate. B-galactosidase expression was measured 48 hours after
transfection by colorimetric assay. For comparison purposes, in each
cell type, the levels of B-gal expression were adjusted to show relative
expression by normalizing the B-gal expression of the gWiz vector to
100%.
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