SmartGlow™ DNA Stains are ideal for excitation of nucleic acids with UV or visible blue light transilluminators. Unlike EtBr, SmartGlow is non mutagenic and does not require special methods of disposal.

SmartGlow PS (Pre Stain) can be used as a direct replacement for Ethidium Bromide in agarose and polyacrylamide gel electrophoresis. The stain emits green fluorescence when bound to dsDNA,  ssDNA and RNA.  SmartGlow PS exhibits excitation peaks at 290nm and 490nm, allowing it to be used with UV and blue light.

Protocol for SmartGlow PS

1. Prepare 100ml of agarose or polyacrylamide solution.
2. Add 5ul of SmartGlow PS stain to the gel solution before pouring gels.
3. For enhanced results, add SmartGlow PS to the running buffer at a ratio of 2.5ul to 5ul per 100ml. Adding SmartGlow PS to the running buffer will result in increased sensitivity and better detection of small quantities of nucleic acid.
4. After electrophoresis is complete, view the gel using a UV or blue light illuminator

SmartGlow™ LD (Loading Dye) is supplied at 6X concentration and is added directly to the samples. No dye needs to be added to the gel or running buffer. After electrophoretic separation, view and document your results using a UV or blue light illuminator. SmartGlow™ LD emits green fluorescence when bound to dsDNA, ssDNA and RNA.

Protocol for SmartGlow LD

1. Prepare agarose for polyacrylamide solution.
2. Pour gels.
3. Mix SmartGlow LD with samples and DNA markers at a 1:5 (dye to sample) dilution.
4. After electrophoresis is complete, view the gel using a UV or blue light illuminator

Key Features

• Replaces hazardous EtBr
• Excitation by UV or blue light
• Non-mutagenic, environmentally safe
• Two types available: PS (Pre-Stain) or LD (Loading Dye)