Dyes

highQu 1Step RT qPCR master mixes in combination with a blend of thermostable and extremely active Reverse Transcriptase & advanced RNase Inhibitor (RT Mix) allow for a single step one tube RT qPCR. 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/GC rich templates and guaranty rapid extension with early Ct va

ALCIAN BLUE 8 GX ALC298 (Ingrain Blue 1) CAS number: [33864-99-2] C56H68N16S4Cl14Cu MW: 1298.88 Dye content: approx. 50%

highQu ALLin™ Hot Start Taq DNA Polymerase is the superior sensitive enzyme. The activity at room temperature is blocked by small molecular inhibitor. Enzyme becomes active only after heating what allows for highly specific and extremely sensitive amplification, no primer dimer formation and no background. In combination with the optimized ALLin™ buffer enzyme provides higher success rates in demanding PCR applications like amplification of crude, complex or longer templates and fast cycling. AL

ALLin™ Isothermal 1Step RNA Amplification Kit enables detection of < 5 target RNA molecules in a short time of 30 minutes without the use of PCR cycler. An RT5 Mix, the blend of a thermostable reverse transcriptase and highly efficient RNase Inhibitor is included in the kit to initially synthesize cDNA from RNA templates. The cDNA is amplified by Bst polymerase. Kit includes a 2X master mix with optimized high-performance buffer, dNTPs and a recombinant Bst Polymerase large fragment having stron

ALLin™ Isothermal DNA Amplification Kit enables detection of as little as 5 target DNA molecules in a short time of 20 minutes even without the use of a thermal cycler. The Kit includes a 2X master mix with optimized high-performance buffer, dNTPs and a recombinant Bst Polymerase large fragment having strong 5’ - 3’ strand displacement activity and efficient 5’-3’ polymerase activity working at 55-70°C. The Polymerase has neither 5’ - 3’ nor 3’ - 5’ exonuclease activity and retains only minor re

highQu ALLin™ Taq DNA Polymerase is the versatile engineered enzyme which in combination with the optimized ALLin™ buffer provides higher success rates in demanding PCR applications like amplification of complex templates, crude sample PCR and fast cycling. ALLin™ Taq DNA Polymerase has the same PCR accuracy like Taq DNA Polymerase, 4.5 x 10^4 (a number of correct nucleotides incorporated before the error occurs) and produces A-tailed products suitable for ligating into TA cloning vectors. The c

AMIDO BLACK 10B AMB603 (Naphtol Blue Black) CAS number: [1064-48-8] C22H14N6O9S2Na2 MW: 616.5 Dye content: approx. 80%

AZURE A AZU416 CAS number: [531-53-3] C14H14SN3Cl MW: 291.8 Dye content: approx. 80%

AZURE B AZU417 CAS number: [531-55-5] C15H16SN3Cl MW: 305.88 Dye content: approx. 75%

BASIC FUCHSIN BSF410 CAS number: [632-99-5] Certified Grade, Biologically tested C20H19N3HCl MW: 337.85 Dye content: min 80% Solubility: water, 2 mg/ml

BRILLIANT GREEN, Certifiable Grade BRG001 CAS number: [633-03-4] Malachite Green G C27H34N2O4S MW: 482.6 Dye content: ≥ 85%

CRESOL RED CRE350 CAS number: [1733-12-6] (O-Cresolsulfonphthalein) C21H17O5S MW: 382.4 Dye content: approx. 95%

CRESOL RED, Sodium salt CRE300 CAS number: [62625-29-0] (O-Cresolsulfonphthalein) C21H17O5SNa MW: 404.4 Dye content: approx. 95% Solubility: water

highQu ALLin™ Hot Start Taq DNA Polymerase is the superior sensitive enzyme The activity at room temperature is blocked by small molecular inhibitor. Enzyme becomes active only after heating what allows for highly specific and extremely sensitive amplification, no primer dimer formation and no background. In combination with the optimized ALLin™ buffer enzyme provides higher success rates in demanding PCR applications like amplification of complex or longer templates and fast cycling. ALLin™ Hot

highQu ALLin™ Taq DNA Polymerase is the versatile engineered enzyme which in combination with the optimized ALLin™ buffer provides higher success rates in demanding PCR applications like amplification of complex templates, crude sample PCR and fast cycling. ALLin™ Taq DNA Polymerase has the same PCR accuracy like Taq DNA Polymerase, 4.5 x 10^4 (a number of correct nucleotides incorporated before the error occurs) and produces A-tailed products suitable for ligating into TA cloning vectors. The c

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 ready to use DNA ladders are mixtures of highly purified plasmid digests and PCR products. The high ladder purity allows for exceptional stability and room temperature storage. Ladders are ready to be directly loaded on agarose gels and are supplied with the loading dye solution for probe DNA. They provide sharp bands for DNA sizing and allow for approximate DNA quantification by comparing the amount of DNA of the band similar in size to your sample band. Gel casting: Choose the appropria

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.

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