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Multiple Options

  • Supplied as a ready to use 40mM mix or a set of 4 separate 100mM solutions
  • Free of impurities and inhibitors that reduce sensitivity and yield
  • No nuclease, protease or nickase activity
  • >99% pure, purified by HPLC

The success of your PCR reaction depends on the quality of the starting materials. Accuris dNTP’s are purified by HPLC in a strict process that results in greater than 99% purity. The stringent purification process eliminates PCR inhibitors such as tetraphosphates and pyrophosphates that can interfere with the sensitivity of your PCR and reduce yields.

Extensive quality control testing is performed to ensure the dNTPs are free of nuclease, protease and nickase activity. Each lot is performance tested in standard PCR, long PCR and qPCR reactions to assess reproducibility and sensitivity.

The 40mM dNTP Mix is a single tube that contains premixed dNTPs at a concentration of 10mM each. The 100mM dNTP Set contains four individual tubes, one each of dATP, dCTP, dGTP and dTTP. The nucleotides are supplied in ultra-pure water as an ammonium salt. Both the set and mix are stable for 24 months when stored at -20ºC.


Multiple Options

  • Superior sensitivity and fast cycling with exceptional results
  • Ideal for low copy number templates
  • Early Ct values and detection across a broad dynamic range
  • Ready to use 2x mastermix
  • Accuris Hot-Start Taq included for greater specificity and accuracy
  • Inert blue tracking dye assists with accurate pipetting

Supplied as a ready-to-use 2X master mix, qMax Green has been engineered for high sensitivity, fact cycling and excellent reproducibility. Accuris Hot Start Polymerase provides accurate PCR of a variety of templates including low copy number and difficult sequences, while the proprietary qMax Green intercalating dye exhibits higher fluorescence and lower PCR inhibition than other popular green dyes.

These two components are supported by a specially formulated buffer with an exacting combination of salts, PCR enhancers, stabilizers and pH that results in earlier Ct values and a high specificity across a broad dynamic range.  An inert blue dye is also mixed into the qMAX Green to allow easy visualization during pipetting.


Multiple Options

  • RNA to cDNA to qPCR in one tube
  • High purity enzyme formulation for enhanced stability and performance
  • Blue dye facilitates pipetting and visualization in plates
  • Accuris Hot-Start Taq allows for preparation at room temperature

Accuris qMAX™ One Step Kits allow for highly sensitive real time RT-qPCR assays to be performed directly from RNA templates.  Workflows are simplified with optimized formulations of ready-to-use 2X qPCR master mix and 20X reverse transcriptase.

Optimized buffer includes powerful RNase inhibitors and an extremely thermostable MMLV-derived reverse transcriptase enables robust first strand cDNA synthesis.  Accuris Hot Start Taq uses an antibody mediated hot start mechanism allowing for sample preparation at room temperature.   Only after an initial incubation at 95C will the Taq become active, so non-specific amplification is greatly reduced.  An inert blue dye is included in the Taq master mix to help simplify pipetting and reduce errors.

All Accuris One-Step Kits are compatible with standard and fast cycling protocols and provide increased sensitivity, speed and reproducibility for a broad range of samples and targets.  The polymerase mix is available with different levels of ROX reference dye for compatibility with all qPCR instruments.

Three versions of our One Step qPCR kits are available.


Multiple Options

The Accuris cDNA Synthesis Kit is a 2-tube format for easy reaction set up and is ideal for 4pg to 0.5µg of input RNA.  One tube includes our exceptionally stable Reverse Transcriptase combined with a potent RNAse inhibitor, and the other tube contains a 5X reaction buffer with an optimal mixture of anchored oligo (dT) primers and random hexamers to produce a nonbiased population of cDNA.


Multiple Options

  • Same high efficiency for multiplex and singleplex reactions
  • Includes Accuris Hot Start Taq Polymerase for greater specificity and accuracy
  • Compatible with popular hydrolysis and beacon probes
  • Ready to use 2x mastermix
  • Early Ct values and detection across a broad dynamic range

Optimized for use with TaqMan™, Scorpions® and molecular beacon probes, qMax Probe qPCR Mix is a ready-to-use formulation for real time quantitative assays. qMax Probe utilizes Accuris Hot Start Taq Polymerase or robust PCR with a variety of templates. A specially formulated buffer provides optimal conditions for both superior polymerase function and probe detection, resulting in earlier Ct values and a broad detection range. Complicated, multiplex reactions can be performed without any loss in performance or decrease in detection. The 2X mix requires little, if any optimization and can be used with both fast and standard protocols. 

qMax Probe qPCR Mix can be used to detect any DNA template, including genomic DNA and cDNA. Available in high, low and no ROX formulations, qMax Probe is compatible with most qPCR instruments. To check compatibility with a specific instrument, visit www.accurisusa.com/PCRselector.


Multiple Options

  • Superior sensitivity and fast cycling with exceptional results
  • Ideal for low copy number templates
  • Early Ct values and detection across a broad dynamic range
  • Ready to use 2X Mastermix

Supplied as a ready-to-use 2X master mix, qMax Green has been engineered for high sensitivity, fact cycling and excellent reproducibility. Accuris Hot Start Polymerase provides accurate PCR of a variety of templates including low copy number and difficult sequences, while the proprietary qMax Green intercalating dye exhibits higher fluorescence and lower PCR inhibition than other popular green dyes.


# W20-105

Molecular Biology Grade, USP Purified Wa ter, 1L, 6/PK