evoglow® Basic Kit
The basic kit was composed for easy cloning of the evoglow®-genes into the customer-specific host- and vector systems. It comprises three different variants of evoglow®-proteins, either with and without a STOP-codon (6 plasmids) on high-copy plasmids. The plasmids replicate well in E. coli and are ideal templates for PCR. They furthermore bear a variety of restriction sites for direct cloning in specific vector-systems.
evoglow® Express Kit
The evoglow® express kit comprises a variety of plasmids designed for efficient expression in a wide host range of gram-negative host organisms. The proteins can be expressed either under control of the inducible T7-promotor as well as in a constiutive manner (kan-promotor).
evoglow® Fusion Kit
The evoglow® fusion kit was designed to create transcriptional protein fusions. It contains plasmids on which the evoglow®-gene are flanked by symmetrical multiple cloning sites (MCS) which enables cloning via a singular restriction site i.e. for conducting promotor activity studies or further physiological investigations.
evoglow® Yeast Kit
The evoglow® yeast kit was created to enable expression of the fluorescent proteins in yeasts and related organisms. It comprises plasmids on which the evoglow® genes are controlled by different yeast promotors (Gal and Act) and you can choose between plasmids that contain a single evoglow® gene or a fusion of two genes per plasmid.
evoglow® Clostridia Kit
The evoglow clostridia kit was designed to express evoglow in Clostridia. It comprises the plasmids pGlow-C-Bs2 (Bacillus subtilis) and pGlow-C-Pp1 (Pseudomonas putida) for Gram-positive and Gram-negative bacteria respectively. The genes are cloned SacI / BamH1 into multiple cloning site of pUCC18 allowing individual subcloning under the control of the promotor of your choice.
Please contact us at info@jenabioscience.com for codon usage optimized variants of evoglow fluorescent proteins.
Selected References
- Drepper et al. (2007) Reporter proteins for in vivo fluorescence without oxygen. Nature Biotech. 25 (4):443
- Tielker et al. (2009) Flavin Mononucleotide-Based Fluorescent Protein as an Oxygen-Independent Reporter in Candida albicans and Saccharomyces cerevisiae. Eukaryotic Cell 8 (6):913
- Ernst et al. (2009) Responses to hypoxia in fungal pathogens. Cellular Microbiology 11 (2):183
- Kensy et al. (2009) Validation of a high-throughput fermentation system based on online monitoring of biomass and fluorescence in continuously shaken microtiter plates. Microbial Cell Factories 8:31
- Huber et al. (2009) Robo-Lector – a novel platform for automated high-throughput cultivations in microtiter plates with high information content. Microbial Cell Factories 8:42
Please contact info@jenabioscience.com with questions or inquiries.

