Reagents for electrophoresis

IMIDAZOLE, Biotechnology Grade IMD508 CAS number: [288-32-4] pKa: 6.95 Useful pH: 6.2 - 7.8 C3H4N2 MW: 68.08 Purity: min. 99% Melting Range: 88 - 92 °C Insolubles: < 0.1% DNase, RNase Activity: none detected Color: white to slightly off - white Solubility (0.1 M): clear/colorless

CAS number: [2044-56-6] C 12 H 25 LiO 4 S MW: 272.33 Purity: min. 99%

CAS Number: [145224-94-8] [2-(N-Morpholino)ethanesulfonic Acid] C 6 H 13 NO 4 S . H 2 O MW: 213.25 Purity: min. 99.5% pKa(25°C): 6.10 ± 0.05% pH (1%, H2O): 3.5 - 4.1 Heavy metals: max. 0.15 ppm Chloride: max. 0.01% Sulfate: max. 0.05% Solubility (10%, water): clear / colorless Dnase/Rnase/protease activity: none detected

CAS number: [71119-23-8] Ultra Pure Grade [2-(N-Morpholino)ethanesulfonic Acid, Sodium salt] C 6 H 12 NO 4 S.Na MW: 217.24 Purity: min.99.5% Solubility (33%, in water): clear / colorless pH (1% water): 9.0 - 10.5 Heavy metals (as Pb): max. 5 ppm UV Absorbance (33% water) 290 nm: max.0.10 Dnase / Rnase / Protease activity: none detected

pH: 6.8 - 7.2 Dnase and Rnase: none detected Sterile filteredFormulation: 200mM MOPS

CAS number: [71119-22-7] C 7 H 14 NO 4 S . Na MW: 231.25 Purity: min 99.5% pH (0.1M, water): 9.5 - 10.5 Solubility (1M, water): clear / colorless Heavy metals (as Pb): max. 10 ppm A260nm: max. 0.05 A280nm: max. 0.03 Dnase / Rnase / Protease: none detected

CAS Number: [1132-61-2] C 7 H 15 NO 4 S MW: 209.27 Purity: min. 99.5% pH (10%, water): 3.0 - 5.0 Heavy metal (as Pb): max. 10 ppm A260 (1M, water): max. 0.05 Solubility (10% water): clear / colorless Dnase / Rnase activity: none detected

N-DODECYL ß-D-MALTOSIDE DDM001 Nonionic detergent -20 °C CAS number: [69227-93-6] C24H46O11 MW: 510.6 Purity: > 98%

StainIN™ eco-RED Nucleic Acid Stain, a 10000X concentrated aqueous solution is a significantly safer alternative to ethidium bromide. It is same easy to use, twice as sensitive and much more secure. At least twice as economical as competing products, this novel DMSO-free stain can be also used and disposed with less environmental and health concerns compared to ethidium bromide. StainIN™ eco-RED is a fluorescent dye that allows detection of >0,1 ng of DNA in both agarose and polyacrylamide gels.

N-LAUROYL SARCOSINE SLS004 CAS number: [137-16-6] C15H28NaO3 MW: 293.39 Purity (HPLC): > 99% pH (10%, H2O, 25 °C): 7.0 - 9.0 Lauric acid: < 0.1% Absorbance: 280 nm <0.06 260 nm <0.08

N-LAUROYL SARCOSINE, Sodium Salt, Reagent Grade SLS002 CAS number: [137-16-6] C15H28NaO3 MW: 293.39 Purity: > 95% pH (10%, H2O,25 °C): 7.5 - 8.5 Sodium Laurate: < 4.0%

n-OCTYL-ß-D-GLUCOPYRANOSIDE (n-Octyl-α-glucoside) Reagent Grade OGP101 -20°C Non-ionic detergent used to solubilize membrane proteins. Dialyzable detergent. CAS number: [29836-26-8] C14H28O6 MW: 292.40 Purity: ≥ 98% Specific Rotation: -32.0 to -28.0

CAS Number: [9016-45-9] MW 603(AVG) HLB Number: 13.1 Density (20°C): 1.06 Solubility (5%, H 2 O): clear / haze free Refractive Index: 1.48 - 1.52 Color: colorless

ORANGE G, Sodium salt ORA787 High purity Grade. Suitable for use as tracking dye in nucleic gel electrophoresis. -20 °C CAS number: [1936-15-8] C16H10N2O7S2Na MW: 452.4 Dye content: min. 80%

highQu qPCR master mixes are based on the small molecular inhibitor technology Hot Start PCR allowing to achieve highest sensitivity and specificity under both standard and fast qPCR cycling conditions. They provide excellent results on both AT and GC rich templates and guaranty rapid extension with early Ct values with minimum or no optimization. Our master mixes are supplied with PCR Water to guaranty the best performance. To suit the broad instrument range the ORA™ qPCR Green Master mixes are

High Resolution Melting analysis (HRM) is a fast and simple technique for identification of DNA sequence variations. It allows identifying single nucleotide differences by detecting minor changes in qPCR melting curves. highQu ORA™ HRM qPCR Mix includes a proprietary intercalating saturating dye showing no inhibition for PCR. The dye has the same affinity for both AT or GC rich sequences what leads to highest accuracy in genotyping. The hot-start function in the mix is based on the small molecul

ighQu qPCR master mixes are based on the small molecular inhibitor technology Hot Start PCR allowing to achieve highest sensitivity and specificity under both standard and fast qPCR cycling conditions. They provide excellent results on both AT and GC rich templates and guaranty rapid extension with early Ct values with minimum or no optimization. ORA™ SEE qPCR mixes provide an additional advantage of a simplified tracking of the process, as they are colored with an inert blue dye to make samples

highQu qPCR master mixes are based on the small molecular inhibitor technology Hot Start PCR allowing to achieve highest sensitivity and specificity under both standard and fast qPCR cycling conditions. They provide excellent results on both AT and GC rich templates and guaranty rapid extension with early Ct values with minimum or no optimization. ORA™ SEE qPCR mixes provide an additional advantage of a simplified tracking of the process, as they are colored with an inert blue dye to make sample

highQu qPCR master mixes are based on the small molecular inhibitor technology Hot Start PCR allowing to achieve highest sensitivity and specificity under both standard and fast qPCR cycling conditions. They provide excellent results on both AT and GC rich templates, in multiplexing and guaranty rapid extension with early Ct values with minimum or no optimization. ORA™ SEE qPCR mixes provide an additional advantage of a simplified tracking of the process, as they are colored with an inert blue d

highQu qPCR master mixes are based on the small molecular inhibitor technology Hot Start PCR allowing to achieve highest sensitivity and specificity under both standard and fast qPCR cycling conditions. They provide excellent results on both AT and GC rich templates, in multiplexing and guaranty rapid extension with early Ct values with minimum or no optimization. ORA™ SEE qPCR mixes provide an additional advantage of a simplified tracking of the process, as they are colored with an inert blue d