GreenSafe DNA Gel Stain
A safe alternative of Ethidium Bromide (EtBr)
GreenSafe DNA Gel Stain replace toxic Ethidium Bromide (EtBr) for the visualization of doublestranded DNA, single-stranded DNA, and RNA in Agarose and Polyacrylamide Gel Electrophoresis.
Detailed information:
Advantages & Features
- Easy-to-Use: replace EB with without changing your current imaging system.
- Superior signal to noise ratio.
- Safe: Non-toxic, non-mutagenic and non-carcinogenic by appropiate Quality and Safety Tests.
- Sensitive: Increase your sensitivity by reducing nonspecific background fluorescence, even for small fragments.
- Save-time: convenient ready-to-use format.
- Versatile: compatible with a wide variety of gel reading instruments.
Specifications
- Concentration: 25.000 X
- Excitation spectra: 270-490 nm (Tree fluorescence excitation peaks: 270 nm, 295 nm and one strong excitation peak 490 nm
- Excitation maximum, nm: ≈ 490 nm
- Emission maximum, nm: ≈530 nm
- Excitation light source: UV
Includes
Includes for 1 mL:
– 1 mL GreenSafe DNA Gel Stain (sufficient up to 25 liters of agarose)
Download documentation
Datasheet MSDSApplications
- Non-carcinogenic alternative to Ethidium Bromide.
- Detection of DNA or RNA in Agarose gels by pre-staining or post-staining.
Quality Control
- Rigorous quality control standards to guarantee lot-to-lot consistency.
Storage, Shipping & Guarantee
- Shipped in: Ambient temperature.
- Storage: between 2°C to 25°C protected from light. 4ºC recommended for long-term storage.
Citations
- Ghadamnan, Elmira. Characterization of Tick-Associated Microbiota in Spain Using a Nanopore-based Metabarcoding Approach: Insights into Potential Zoonotic Pathogens. 2023.
- Díaz del Moral, S. (2023). Functions of the Wilms’ tumor suppressor gene (Wt1) in embryonic and adult myocardium.
- PLANT, B. A. I. M. MALAYSIAN JOURNAL OF BIOCHEMISTRY & MOLECULAR BIOLOGY.
- García-Sánchez, A. M., Miller, A. Z., Caldeira, A. T., & Cutillas, C. (2021). Bacterial communities from Trichuris spp. A contribution to deciphering the role of parasitic nematodes as vector of pathogens. Acta Tropica, 106277.
- Fitriyah, F., Faramitha, Y., Sari, D. A., Kresnawaty, I., Panji, T., & Santoso, D. (2021, December). Improved direct lysis PCR amplification method of microalgal culture for sequencing and species identification. In IOP Conference Series: Earth and Environmental Science (Vol. 948, No. 1, p. 012013). IOP Publishing.
- Pediconi, Natalia, et al. “Design and Synthesis of Piperazine-Based Compounds Conjugated to Humanized Ferritin as Delivery System of siRNA in Cancer Cells.” Bioconjugate Chemistry (2021).
- Musso, N., Costantino, A., La Spina, S., Finocchiaro, A., Andronico, F., Stracquadanio, S., … & Emmanuele, G. (2020). New SARS-CoV-2 Infection Detected in an Italian Pet Cat by RT-qPCR from Deep Pharyngeal Swab. Pathogens, 9(9), 746.
- Musso, N., Costantino, A., La Spina, S., Finocchiaro, A., Andronico, F., Stracquadanio, S., … & Emmanuele, G. (2020). New SARS-CoV-2 Infection in a Pet Cat with Severe Lung Disease in Italy.
Safety Statements
This product is developed, designed and sold exclusively for Research purposes and in vitro use only (RUO). The product was not tested for use in diagnostics or for drug development, nor is it suitable for administration to humans or animals. For more info, please check its Material Safety Data Sheet available in this website.
