The dye is Orange G and Xylene Cyanol FF (XC)! It is possible to take UV photos without any dye shadows in the central part of the gel.
"6 X Loading Buffer Double Dye" is a reagent added when preparing nucleic acid samples for electrophoresis. By not using BPB, it is possible to take UV photographs without any dye shadows in the center of the gel. As an example of use, add 2μl of this product to a 10μl DNA sample solution, mix by pipetting several times, and then gently inject (apply) 10μl of the mixture into the wells of an agarose gel to perform electrophoresis. 【Features】 - Added when preparing nucleic acid samples for electrophoresis - Used at 1/6 the amount relative to the sample volume - BPB-free - Less prone to band smiling compared to glycerol *For more details, please refer to the related links or feel free to contact us.
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【Product Contents】 ■Components: 6 x Loading Buffer Double Dye ■Volume: 1 ml x 3 ■Storage: Room temperature ■Notes ・0.3% (w/v) Orange G ・0.03% (w/v) Xylene Cyanol FF ・15% (w/v) Ficoll PM400 ・10 mmol/l Tris HCl (pH 7.5) ・50 mmol/l EDTA (pH 8.0) *For more details, please refer to the related links or feel free to contact us.
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【Usage】 ■ Added when preparing nucleic acid samples for electrophoresis *For more details, please refer to the related links or feel free to contact us.
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Our company is a product development-oriented enterprise that utilizes biotechnology. We develop and manufacture in vitro diagnostic pharmaceuticals (such as pregnancy tests and ovulation tests), diagnostic drugs for environmental, food, and animal and plant diseases, and reagents for genetic engineering research, using our expertise in gene and antibody technology. We hold manufacturing registration and manufacturing and sales licenses for both human and animal products, with over 30 years of experience in the manufacture of in vitro diagnostic pharmaceuticals. Additionally, we are engaged in personalized medicine, advancing research and development of diagnostic drugs using genetic polymorphism analysis and gene expression analysis.