English
The principle of the Nucleofector™ technology:
By applying electrical impulses, small pores are briefly created in the cell membrane. An interplay of preprogrammed nucleofection protocols and coordinated reagents results in optimally adapted conditions for a successful transfection for the cell type used. The substrate is not only taken up by the cytoplasm, but also by the cell nucleus due to the optimized conditions. This process enables high transfection rates with an efficiency of up to 99%.
We offer the following platforms:
The new MaxyGene II enables protocol optimization over 6 different temperature zones, each with 16 slots for 0.2 ml reaction vessels, and replaces conventional gradient technology. Thanks to the individual temperature control, 6 different primer pairs can also be used in one run.
The two different models of the Axygen Gel Documentation can be used for the visualization of DNA and colored proteins in a gel as well as their photo documentation under laboratory conditions.
Both models work with UV, White Light and Blue Light Imaging.
The AXYGDBL-1000 model has a tablet PC and works with blue light LED illumination.
The AXYGD-1000 model did not include a PC.
Main features:
Lonza's FlashGel™ system enables rapid electrophoretic separation of your DNA sample in an agarose gel.
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