Enjoy superior performance and versatility
Instrument Specifications
- Electrical power cord includes adapter for connecting inside most gel documentation systems
- Produces brighter light and more uniform emission than conventional blue light sources
- Provides optimal excitation for SYBR® Safe DNA gel stain
- Optimized for use with other nucleic acid and protein stains such SYBR® Gold, SYBR® Green I & II, SYPRO® Ruby, SYPRO® Orange, and Coomassie Fluor™ Orange stains
Instrument Specifications
- Instrument dimensions: 195 × 325 × 65 mm (11.6 × 12.8 × 2.6 in)
- Viewing surface dimensions: 190 × 190 mm (7.5 × 7.5 in)
- LED life: 50,000 hours
- Complies with the European Community Safety requirements
- This device contains Class 1 LED products
- Light source: light emitting diodes (LED) producing a narrow emission peak centered at ~470 nm
- Included accessories: amber filter unit, viewing glasses, and international power cord
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Figure 1 - Even a 30-second exposure to ethidium bromide and UV reduces cloning efficiency.
Gels loaded with equal amounts of a PCR product (1.25 kb gene fragment from Ultimate™ ORF IOH# 11050) were stained with either SYBR® Safe DNA gel stain (1:10,000 in TBE) or ethidium bromide (0.5 µg/ml in TBE) following electrophoresis. The gel stained with SYBR® Safe stain was visualized on a blue-light box with light emission identical to that produced by the Safe Imager™ transilluminator (S37102). The ethidium bromide-stained gel was visualized using UV transillumination. Bands were excised at defined exposure times. DNA was purified from the gel fragments under identical conditions and used in parallel sub-cloning reactions. Following transformation into OneShot® TOP 10 chemically competent bacteria, three serial dilutions were plated and colonies counted using an Alpha Innotech imaging system. A plot of the experiment is shown here. |
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Figure 2 - Use of SYBR® Safe Stain and the Safe Imager™ Transilluminator causes minimal DNA damage.
Equivalent fractions of supercoiled DNA stained with SYBR® Safe DNA Gel Stain or ethidium bromide were exposed to blue light (Safe Imager™ Transilluminator, Invitrogen) (A) or UV light (B), respectively, for defined periods of time and evaluated by agarose electrophoresis. A slowermigrating species is indicative of a linear or relaxed circular vector resulting from DNA nicking or strand breaks. |






