For easy and safe addition of ethidium bromide in solutions. Add one drop per 50 ml of solution to obtain a concentration of 0.5 µg / ml. Bottle is waterproof and provides protection against UV.
• Quick and easy • No pipetting required, delivers a small amount of stain to the agarose gel via a special paper backing • Place the card on the gel and wait: 8-10 min. for 1% agarose gels and 3-5 min. for 0.8% agarose gels • Each card will stain a gel up to 7 x 7 cm in size
High sensitivity even for small fragments, superior signal to noise ratio, can be used in a classical gel staining procedure as well as in post staining procedures, 4 - 6 µl in 100 ml of agarose.
• For the labeling of nucleic acids • Non-carcinogenic alternative to ethidium bromide • Storage solution without DMSO
3 versions: • Midori Green Advance: high sensitivity for small fragments, background noise reduction, dye to be added during the preparation of the gel or following the migration, 4 - 6 µl for 100 ml of agarose; main excitation wavelength 490 nm / secondary 290 nm; emission wavelength 530 nm • Midori Green Direct: mix directly with the samples ratio 10:1 , background noise reduction, included a dye load; main excitation wavelength 490 nm / secondary 270 nm; emission wavelength 530 nm • Midori Green Xtra: ultra sensitive dye when excited in blue or blue / green light (detecting nucleic acids aquantity detection lower than 4 ng), for excitation in the UV rather choose the Midori Green Advance, very low background noise, 4 - 8 µl for 100 ml of agarose; main excitation wavelength 482 nm / secondary 250 nm; emission wavelength 509 nm
• Non-hazardous, non-mutagenic and non-toxic alternative to ethidium bromide • Ready-to-use 6X charge buffer for direct mixing with samples • Contains 3 migration dyes: bromophenol blue, xylene cyanol and orange G • Excitable by UV and blue light • Excitation/emission spectrum: 495 (pic 1), 260 (pic 2) nm / 540 nm
• Stable and sensitive dye for nucleic acids visualization (RNA and single and double stranded DNA) • Alternative to the use of BET, safe for the environment • Presents the same excitation and emission spectra as BET • GelRed stained nucleic acids can be used in cloning and sequencing • 10000 X in water concentration dye • Available in three packs: 0.1; 0.5 and 10 ml • Main excitation wavelength 290 nm / secondary 520 nm • Emission wavelength 595 nm
• For staining nucleic acids • Alternative non mutagenic non cytotoxic and no ethidium bromide • More sensitive than ethidium bromide and SYBR Green • Extremely stable: long-term storage at room temperature and can be microwaved • Dye to be added during the preparation of the gel or staining afterwards • Easy to use • Main excitation wavelength 505 nm / secondary 270 nm • Emission wavelength 530 nm
• Deep blue bands visible by the naked eye following 5-30 min light exposure • Ultrasensitive detection, as little as ~1 ng DNA • Simplified DNA band excision, without the need for DNA damaging UV light • Compatible with downstream applications such as sequencing and cloning • We advise the use of orange G rather than the use of blue bromide • Photo capture possible without imager
• Dye visible to the naked eye after 5 to 30 minutes of exposure to light • Ultrasensitive, band visualization up to 1 ng of DNA • Excision of the bands of interest without the use of a UV lamp • Dye compatible with subsequent use of DNA for sequencing and cloning • The use of bromophenol blue (found in some loading buffers) is not recommended, it is preferable to use G • Picture taking possible without imager
• For nucleic acid labelling • Non-mutagenic and non-cytotoxic alternative to ethidium bromide • More sensitive than ethidium bromide or SYBR GREEN • Dye to be added after migration • Main excitation wavelength 500 nm/secondary between 250 and 300 nm • Emission wavelength 530 nm