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PR1MA™ Hot Start Taq
- Exceptional sensitivity for low-copy PCR
- Ideal for multiplex PCR and amplification of GC-rich DNA
- Same enhanced features as PR1MA Taq Polymerase
- Buffer optimized for fast cycling and reproducibility
Engineered for controlled polymerase activity, PR1MA™ Hot Start Taq is bound with a monoclonal antibody that blocks enzyme activity. This allows reactions to be set up at room temperature without the risk of non-specific amplification.
When samples are ready, the reaction mixture is heated to 95°C to denature the antibody and initiate the reaction. Similar to the standard PR1MA™ Taq, Hot Start Taq is provided with a 5X buffer, or in a ready-to-use 2X Master Mix. The Master Mix can be ordered with or without an incorporated red gel loading dye. The Red Dye Master Mix incorporates a red-loading dye that allows amplified samples to be loaded directly on an agarose gel. The red color aids in visualization during pipetting, and higher density of the buffer ensures that the samples will drop into the gel wells.
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PR1MA™ High Fidelity Polymerase
- 50X higher fidelity than Taq DNA polymerase
- Works with crude DNA sample
- Ideal for cloning, mutagenesis and microarrays
- Produces blunt end products, to clone directly into blunt end vectors
- Optimized buffer system with unique PCR enhancers
For applications requiring highly accurate amplification, choose PR1MA™ High Fidelity DNA polymerase. Modified for better solubility and higher activity across a broad range of ionic conditions, this polymerase will amplify a wide range of targets, including those that are GC or AT rich as well as crude samples.
A 3'-5' proofreading exonuclease activity and an error rate of 4.55×10-7 makes PR1MA™ High Fidelity DNA Polymerase the perfect partner for cloning applications. The supplied 5X buffer with dNTPs is optimized for compatibility with a variety of targets.
Specifications
| Item | Description | Volume |
| PR1000-HF-S | PR1MA™ High Fidelity DNA Polymerase | 20 Units (Sample) |
| PR1000-HF-200 | PR1MA™ High Fidelity DNA Polymerase | 200 Units (2 U/p1) |
| PR1000-HF-500 | PR1MA™ High Fidelity DNA Polymerase | 500 Units (2 U/p1) |
| PR1000-HF-1000 | PR1MA™ High Fidelity DNA Polymerase | 1,000 Units (2 U/p1) |
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PR1MA™ High Fidelity Hot Start Master Mix
- Leaves an A-overhang for TA cloning
- Ideal for difficult, high GC content sequences
- 10x fidelity of native Taq
- Ideal for long PCR, up to 10kb targets
PR1MA™ High Fidelity Hot Start Mix is a hot start 2x formulation which provides excellent sensitivity in low-copy number assays with 10x higher fidelity than Taq polymerase. The 2x master mix contains proprietary enhancers, an antibody-mediated hot-start mechanism, and a proofreading component for trouble-free PCR reaction assembly and performance.
The pre-optimized Hot Start Master Mix is supplied in a single tube, reducing the number of pipetting steps while improving throughput and reproducibility. The highly efficient buffer formulation and hot-start blend provide the ideal conditions for high-performance PCR and inactivity at room temperature thereby eliminating non-specific amplification.
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PR1MA™ High Fidelity Master Mix
- Leaves a blunt end
- Rapid extension: up to 1 kb per 15 seconds
- 100x fidelity of native Taq
- Ideal for shorter, less complex targets
A 2x formulation which provides extreme sensitivity in low copy number assays with 100x the fidelity of native Taq, PR1MA™ High Fidelity Master Mix is perfect for shorter, less complex targets. The 2x master-mix contains proprietary enhancers and a proof-reading component for trouble-free PCR reaction assembly and performance. High Fidelity Master Mix delivers a unique balance of PCR sensitivity, high fidelity, versatility, and tolerance to inhibitors.
The pre-optimized Master Mix is supplied in a single tube, reducing the number of pipetting steps while improving throughput and reproducibility. The highly efficient buffer formulation provides the ideal conditions for high-performance PCR.
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PR1MA™ qMAX One-Step RT-qPCR Kits
- RNA to cDNA to qPCR in one tube
- High purity enzyme formulation for enhanced stability and performance
- PR1MA™ Hot-Start Taq allows for preparation at room-temperature
- Compatible with all qPCR instruments
- Available for green fluorescence or probe detection
Both 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.
Two versions of our One-Step qPCR Kits are available:
PR1MA™ qMAX Green One-Step Kits incorporate our proprietary intercalating dye which exhibits higher fluorescent and lower PCR inhibition than other popular dyes such as SYBR.
PR1MA™ qMAX Probe One-Step Kits are optimized for use with popular TaqMan, Scorpions, and molecular beacon probes.
*Please note these
products ship on dry ice. Appropriate shipping charges apply unless
otherwise noted on a quote.
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PR1MA™ SmartCheck DNA Ladders
- Ready-to-use formulation includes loading buffer and tracking dye
- 500 µL suitable for 100 lanes (5 µL per lane)
- Higher intensity reference bands
- Ultra pure production allows economical ambient shipping
Technical Details
Protocol: Briefly vortex the tube and use 5 µL per lane. Additional loading buffer is not required.
Concentration: 0.1 mg / mL
Tracking dye: bromophenol blue and xylene cyanol
Buffer formulation: 10mM Tris-HCl (pH 8.0), 5 mM EDTA, 12.5% glycerol, 0.008% bromophenol blue, 0.008% xylene cyanol
Shipping and Storage: SmartCheck™ DNA Ladders are shipped at ambient temperature. On arrival, store at -20°C for optimum stability and long-term storage up to 15 months.
Production: SmartCheck™ ladders are produced from proprietary plasmids, digested to completion. A multistep chromatography method is used to ensure purity and DNA quality.
Specifications
| Item | Description | Volume |
| PR4005-100 | PR1MA™ SmartCheck™ 50bp DNA Ladder | 500 uL / 100 Lanes |
| PR4005-500 | PR1MA™ SmartCheck™ 50bp DNA Ladder | 5 x 500 uL / 500 Lanes |
| PR4010-100 | PR1MA™ SmartCheck™ 100bp DNA Ladder | 500 uL / 100 Lanes |
| PR4010-500 | PR1MA™ SmartCheck™ 100bp DNA Ladder | 5 x 500 uL / 500 Lanes |
| PR4100-100 | PR1MA™ SmartCheck™ 1kb DNA Ladder | 500 uL / 100 Lanes |
| PR4100-500 | PR1MA™ SmartCheck™ 1kb DNA Ladder | 5 x 500 uL / 500 Lanes |
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PR1MA™ Mammalian Genotyping Kit
- DNA extraction and amplification in 1 hour
- Proprietary lysis buffer optimized for ear punches, tail snips and other mammalian tissues
- Single tube - no organic solvents or clean up procedures
- Enhanced PR1MA™ Hot Start Polymerase included
Traditionally, mammalian genotyping protocols have involved Proteinase K digestion, neutralization, organic extraction and lots of hands on time to get PCR-ready DNA.
The PR1MA™ Mammalian Genotyping Kit is quick and easy to use - add sample to the proprietary lysis buffer and incubate for 5-10 minutes, then add the deactivation buffer and incubate for 10 minutes. The crude lysate can then be amplified using fast PCR PR1MA™ Hot Start Taq Master Mix with red loading dye (included). The kit contains everything needed - just add sample and primers.
PR1MA™ 1 Hour Mammalian Genotyping Kit
|
Item |
Description |
Volume |
|
PR1300-MG-S |
PR1MA™ 1 Hour Mammalian Genotyping Kit |
8 Reactions
(Sample) |
|
PR1300-MG-80 |
PR1MA™ 1 Hour Mammalian Genotyping Kit |
80 Reactions |
|
PR1300-MG-400 |
PR1MA™ 1 Hour Mammalian Genotyping Kit |
400 Reactions |
|
PR1300-MG-800 |
PR1MA™ 1 Hour Mammalian Genotyping Kit |
800 Reactions |
PR1MA™ Genotyping Hot Start Master Mix, 2X Concentration with Red Dye
|
Item |
Description |
Volume |
|
PR1301-HSR-400 |
PR1MA™ Genotyping Hot Start Master Mix, 2X Conc., Red Dye |
400 Reactions |
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Accuris qMAX™ One-Step RT-qPCR kits
- RNA to cDNA to qPCR, in one tube
- High purity enzyme formulation for enhanced stability and performance
- Accuris Hot-Start Taq allows for preparation at room-temperature
- Blue dye facilitates pipetting and visualization in plates
- Available for green fluorescence or probe detection
- Multiplex formulation available for multiple target amplification
Bulk Packaging:
Low Rox and High Rox formulations are available for compatibility with all brands of qPCR cyclers. Please specify when ordering.
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Accuris qMAX™ Probe Bulk Packaging
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.- 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
Low Rox and High Rox formulations are available for compatibility with all brands of qPCR cyclers. Please specify when ordering.
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SmartDye™ Terminator v3.1 Cycle Sequencing Kits
SmartDye™ Terminator v3.1 Cycle Sequencing Kits are engineered to deliver exceptional Sanger sequencing performance with longer, high-quality reads, superior accuracy, and minimal background noise. Built on the trusted Sanger sequencing method, SmartDye™ chemistry ensures reliable sequencing even on difficult templates, including GT-rich regions.
Designed as a direct, economical drop-in replacement for the Applied Biosystems, BigDye™ Terminator v3.1 Cycle Sequencing Kit, SmartDye™ requires no protocol changes, no new mobility shift files, and no recalibration, making the transition seamless for any laboratory.
SmartDye™ Terminator v3.1’s proprietary fluorescently labeled dideoxynucleotide mix, high-fidelity DNA polymerase, and 5X optimized buffer combine to deliver long read lengths and high signal-to-noise ratios. This ensures clean, accurate data interpretation even when sequencing challenging templates.
Main Attributes
- Robust Chemistry
- Based on proven Sanger sequencing technology
- High-quality, long read lengths with low error rates
- Optimized dye chemistry for clear signal separation
- Ideal for templates with high GT repeat content
Flexible Applications
SmartDye™ supports multiple sequencing workflows, including:
- De novo sequencing
- Resequencing
- Finishing applications
Compatible with a wide range of templates:
- PCR products
- Plasmids
- BACs
- Fosmids
Direct Replacement for BigDye™
- Fully compatible with existing BigDye™ v3.1 protocols
- Simply substitute SmartDye™ for BigDye™ no retraining or workflow changes
- Faster reaction times possible (as little as 3 minutes) without sacrificing quality
Cost-Effective Solution
SmartDye™ offers excellent value with ready-to-use premix and 5X buffer. Kits are available in 24, 100, 1,000, 5,000, and 25,000 reaction sizes, supporting labs of all throughput levels. Research also shows SmartDye™ performs well at reduced volumes, as little as 0.15 uL in a 5 uL reaction, further lowering per-reaction cost.
Disclaimer
BigDye™ is a trademark of Applied Biosystems, LLC. SmartDye™ Terminator Sequencing Kits are thirdparty products designed for use in workflows compatible with BigDye™ chemistry. Applied Biosystems, LLC does not manufacture, sponsor, or endorse SmartDye™ products, and is not affiliated with these offerings in any way.
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Accuris qMAX™ One-Step RT-qPCR kits
- RNA to cDNA to qPCR, in one tube
- High purity enzyme formulation for enhanced stability and performance
- Accuris Hot-Start Taq allows for preparation at room-temperature
- Blue dye facilitates pipetting and visualization in plates
- Available for green fluorescence or probe detection
- Multiplex formulation available for multiple target amplification
- Bulk pricing available for high throughput labs and kit manufacturers. Contact us for details
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.
Three versions of our One Step qPCR kits are available:
qMAX™ Green One Step kits incorporate our proprietary intercalating dye which exhibits higher fluorescent and lower PCR inhibition than other popular dyes such as SYBR.
qMAX™ Probe One Step kits are optimized for use with popular TaqMan™, Scorpions, and molecular beacon probes.
qMAX™ Probe One Step Multiplex kits are specifically developed and optimized for efficient probe-based detection of multiple targets in a single reaction well. The Multiplex formulation is comprised of a 20x reverse transcriptase and 2x PCR Mix preparation ideally suited for complex RNA samples including low-copy number viral RNA commonly used in the clinical and research laboratory. qMAX Probe One Step Multiplex kits have been designed to overcome the many challenges of multiplex RT-PCR, by addressing important factors such as the balance between magnesium chloride and deoxynucleotide concentrations, the relative Taq Polymerase and reverse transcriptase concentration, and the ionic conditions of the core reaction buffer.
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.
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PR1MA™ Tn5 2.0 Transposase
PR1MA™ Tn5 2.0 Transposase (Tnp) is a hyperactive retroviral integrase engineered for improved activity, speed, and robustness that is used to construct random next-generation sequencing libraries and to study chromatin structure using targeted ATAC-seq. PR1MA™ Tn5 2.0 can be used to randomly fragment any target and insert unique oligonucleotide adapters in a single reaction which reduces the time and sample requirements relative to traditional next-gen sequencing library construction.
- Optimal temperature: 55°C
- Inactivation: 40X Stop solution included (2% SDS)
- Storage temperature: -20°C
- 10X Tn5 reaction buffer included
Buffer composition
- 100 mM Tris-HCl
- 100 mM MgCl2
- pH = 7.5
*These products are intended for research use only, not for diagnostic use. The safety and efficacy of these products in diagnostic or other clinical uses has not been established.
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