Gel Electrophoresis Buffers and Diluents
Zymo Research Corporation M-Binding Buffer, 80 ml
M-Binding Buffer (80 ml) for use with EZ DNA Methylation™ bisulfite conversion Kits.Sold individually or as part of a bisulfite conversion kit.
Pion Inc PRIMA HT 50ML
Proprietary buffer for performing PAMPA or µSOL assays. Quantity: 1 bottle; volume: 50 mL per bottle.
Integrated DNA Technologies Inc 10 x 2 mL IDTE pH 8.0 (1X TE Solution)
IDTE (10 mM Tris, 0.1 mM EDTA) is our recommended solution for resuspending and storing single-stranded DNA and RNA oligos. It offers the most stability for the longest duration when compared to oligos stored dry or in water. IDTE is available at pH 7.5 or pH 8.0.
New England Biolabs, Inc. Isothermal Amplification Buffer II Pack – 6 ml (4 x 1.5 ml)
10X Isothermal Amplification Buffer II is optimized for use with Bst 3.0 DNA Polymerase. This buffer provides superior reaction conditions for isothermal amplification applications.
Aqua Solutions Buffer Reagent for Hexavalent Chromium Analysis
Buffer Reagent for Hexavalent Chromium Analysis
Electron Microscopy Sciences Michel's Buffer 1 LT
Our buffers are ideal for maintaining a constant pH during fixation and have an ionic constitution to prevent the extraction of cellular components or the deposition of precipitates of fixative chemicals. The buffers are prepared fresh for each order and conveniently packaged.
Electron Microscopy Sciences Phosphate Buffer 0.1M, pH 6.5 1 LT
Prepared fresh for each order from Sodium Phosphate Monobasic Hydrate and Sodium Phosphate Dibasic Heptahydrate. Non-Sterile. Meant for biological research only. Not to be used for medical or any other purposes.
Lonza Walkersville FlashGel Visualization Glasses
FlashGel Visualization Glasses enable viewing of DNA bands to be recovered using the FlashGel Recovery System. The FlashGel Visualization Glasses enable direct viewing of DNA as it is being recovered. Using the FlashGel System users simply load samples, watch bands migrate and get data in as little as 2 minutes. Direct DNA recovery using The FlashGel Recovery System eliminates agarose gel preparation, band excision and purification. The system delivers highly efficient recovery, free from inhibitors and UV-induced damage, in a simple 5-10 minute protocol.Benefits:Directly visualize bands for recoverySee bands in as little as 2 minutesRecover samples directly without UV light band excision or purificationReal-time separation and documentationWatch band migration as it happensPhotograph gels at the bench without DNA damaging UV lightOutstanding sensitivity and resolution Applications:DNA ElectrophoresisRNA ElectrophoresisContent:FlashGel Visualization Glasses
Nelson Jameson Company 3M Phosphate Buffer 90ml
3M™ Flip-Top Dilution Bottles are ideal diluents for enumeration of microoroganism from food, beverage and environmental samples. The solution is decontaminated through gamma irradiation for long shelf life, and the updated handy flip-top style provides a fast, easy and reliable for sample processing
Zymo Research Corporation Microbial Selection Enzyme, 50 µl
The Microbial Selection Enzyme is able to degrade all forms of DNA and RNA and is used during Host DNA Depletion in the HostZERO™Microbial DNA Kit.
Zymo Research Corporation Microbial Selection Buffer, 5 ml
The Microbial Selection Buffer permits the function of the Microbial Selection Enzyme during Host DNA Depletion in the HostZERO™Microbial DNA Kit.
Zymo Research Corporation Mix & Go E. coli Transformation Kit & Buffer Set, up to 20 ml
The methods eliminate the requirement of heat-shocking and related procedures. Instead, transformation can be performed by adding DNA to prepared Mix & Go cells and the mixture spread directly to a culture plate. Transformation efficiencies typically range from 108–109 transformants/µg of pUC19 DNA but can vary depending on the strain of E. coli. Most E. coli strains respond well to the Mix & Go preparation method and demonstrate fast transformation kinetics.The procedures are easy. Simply culture the E. coli strain of your choice in ZymoBroth™ medium (or SOB), wash and then resuspend the cells in the provided uniquely formulated buffers. The cells are now ready for transformation.