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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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2026 On Target Promo!

 

For a limited time, buy one AccuFi™ High Fidelity Hot Start Master Mix (PR1002-HFHS-100)
and get ONE FREE (PR1002-HFHS-100-VF)

  

For free product, add item PR1002-HFHS-100 at $155.00

PLUS item PR1002-HFHS-100-VF to your cart.

 

Use promo code: OT202

 

Click here for more On Target savings

or see flyer for more details.

 

Promotion valid until 10/31/26 or while supplies last, for eligible U.S. customers.

Prices are in U.S. dollars and exclude freight, taxes, installation, and other applicable charges.

Offers may not be combined with other offers, discounts, or institutional pricing.

Customer must pay the list price on the qualifying item to receive the free item (List Price is reflected in flyer).

Buy-one-get-one offers apply to identical eligible catalog numbers unless otherwise stated.

All terms and conditions apply.


AccuFi™ High Fidelity Hot Start Master Mix

 

Highly accurate amplification.

 

Proofreading enzymes are modified for better sensitivity and higher activity to ensure more reproducible performance with a wide range of targets. 

  • Up to 100X higher fidelity than Taq polymerase
  • Crude DNA sample will not inhibit amplification
  • Ideal for cloning, mutagenesis, sequencing, and microarrays
  • Options for blunt-end or A-overhang products
  • Optimized buffers include PCR enhancers 

Accuris™ AccuFi™ HFHS PCR Mix is an optimized 2X master mix that includes AccuFi™ High Fidelity polymerase, a proprietary reaction buffer system, MgCl2, and ultra-pure dNTPs. The engineered polymerase exhibits rapid extension kinetics (~10 s/kb), enabling efficient fast cycling protocols while maintaining high processivity. The formulation supports robust long-range amplification, with reliable performance on templates exceeding 15 kb.

 

The enzyme possesses both 5’→3’ DNA polymerase activity and intrinsic 3’→5’ exonuclease proofreading activity, resulting in an ultra-low error rate (below the detection limit) compared to Taq DNA polymerase. The high fidelity of the enzyme supports applications where sequence integrity is critical, such as molecular cloning, next-generation sequencing (NGS) library construction, and site-directed mutagenesis.

 

The optimized buffer system enhances amplification efficiency across challenging templates, including GC-rich and partially impure DNA samples, while maintaining high yield and specificity with minimal reaction optimization.

 

Main Attributes

  • Ultra-high fidelity: Exhibits highly accurate DNA synthesis supported by coupled 5’→3’ DNA polymerase activity and intrinsic 3’→5’ exonuclease proofreading
  • Hot Start DNA polymerase: Minimizes nonspecific amplification, reduces background, and enhances reproducibility in PCR
  • Strong amplification performance: Supports efficient amplification across challenging templates, including GC-rich sequences, low-quality, and long-range targets, while maintaining high yield
  • Fast extension rate: Delivers rapid DNA synthesis at approximately 1 kb/10 seconds, supporting accelerated PCR cycling 

Storage
 

Upon receipt, immediately store at -20ºC. Avoid excessive freeze/thaw cycles.
 

Proudly made in the USA! Click here for more made in America products!


PR1MA™ Taq DNA Polymerase

 

Saves time and cost by enabling direct PCR amplification of unpurified templates. PR1MA™ Taq DNA polymerase is a recombinant, truncated (lacks 5’ to 3’ exonuclease activity), highly thermostable DNA polymerase from the thermophilic bacterium Thermus aquaticus. The enzyme is thermostable up to 98°C for polymerase chain reaction assays. It is supplied with 4 M betaine to improve amplification of GC-rich DNA and 30% sucrose to improve amplification from inhibitor-rich substrates such as blood.

  • Lacks exonuclease activity
  • Thermotolerant up to 98°C
  • Resistant to inhibitors, e.g., whole blood
  • Ideal for GC-rich templates
  • Storage temperature: -20°C
  • 10X PR1MA™ buffer, 4 M Betaine, and 30% Sucrose included

Buffer composition

  • 50% glycerol
  • 50 mM Tris-HCl
  • 50 mM KCl
  • 1 mM DTT
  • 0.1  mM EDTA
  • 0.5% Tween-20
  • 0.5% NP-40 substitute
  • pH = 7.5 

Important note: Please be sure to use the buffer provided with this product to ensure optimal results.

 

*These products are intended for research use only, not for therapeutic or diagnostic purposes in humans or animals. The safety and efficacy of these products in diagnostic or other clinical uses has not been established.
 

Proudly made in the USA! Click here for more made in America products!  


PR1MA™ CRISPR/Cas9 Nucleases

 

The RNA-guided endonuclease Cas9, associated with Type II CRISPR/Cas systems, site-specifically digests DNA using a single guide RNA (sgRNA) which it binds to direct it to the complementary sequence. MIDSCI™ offers two traditional versions of Streptococcus pyogenes Cas9 nuclease: CRISPR/Cas9, ideal for in vitro DNA digestion, and CRISPR/Cas9 NLS, for in vivo nuclear localization.

  • Optimal temperature: 37°C
  • Heat inactivation: 65°C for 20 minutes
  • Storage temperature: -20°C

Buffer composition

  • 50% glycerol
  • 50 mM Tris-HCl
  • 50 mM KCl
  • 1 mM DTT
  • 0.1  mM EDTA
  • pH = 7.5 

*These products are intended for research use only, not for therapeutic or diagnostic purposes in humans or animals. The safety and efficacy of these products in diagnostic or other clinical uses has not been established.

 

Proudly made in the USA! Click here for more made in America products!  


PR1MA™ Bst DNA Polymerase

 

PR1MA™ Bst polymerase (patent pending) is a recombinant, truncated, thermostable Bacillus stearothermophilus DNA polymerase with high reverse transcriptase and strand-displacement activities, ideal for isothermal amplification of RNA and DNA targets. PR1MA™ Bst polymerase has increased sensitivity and speed relative to other Bst polymerases and can incorporate dUTP. 

 

Use PR1MA™ Bst polymerase to develop LAMP assays with high sensitivity and specificity.

  • Lacks 5’ to 3’ exonuclease activity
  • Only Bst polymerase in the market with robust RT and DNA polymerase activity
  • Thermostable, working temperature range 64 - 72°C
  • Tolerant to inhibitors
  • Storage temperature: - 20°C

Buffer composition

  • 50% glycerol
  • 50 mM Tris-HCl
  • 50 mM KCls
  • 1 mM DTT
  • 0.1  mM EDTA
  • 0.05% Tween – 20
  • 0.05% NP - 40 substitute
  • pH = 7.5

Important note: Please be sure to use the buffer provided with this product to ensure optimal results.

 

*These products are intended for research use only, not for therapeutic or diagnostic purposes in humans or animals. The safety and efficacy of these products in diagnostic or other clinical uses has not been established.  

Proudly made in the USA! Click here for more made in America products!


PR1MA™ Reverse Transcriptase

 

PR1MA™ reverse transcriptase (RT) is an RNA-dependent DNA polymerase that can be used for complementary DNA (cDNA) synthesis from an RNA template and is ideal for use in molecular amplification assays. PR1MA™ RT is a robust enzyme that works in a broad range of temperatures (40 - 72°C) and has RNase H activity.

  • Optimal temperature: 55°C
  • Heat inactivation: 75°C for 20 minutes
  • Glycerol-free buffer available
  • Storage temperature: -20°C (standard buffer)
  • 10X Isothermal buffer included

Standard Buffer Composition

  • 50% glycerol
  • 10 mM Tris-HCl
  • 100 mM KCl
  • 1 mM DTT
  • 0.1  mM EDTA
  • pH = 7.5

Important note: Please be sure to use the buffer provided with this product to ensure optimal results.

 

*These products are intended for research use only, not for therapeutic or diagnostic purposes in humans or animals. The safety and efficacy of these products in diagnostic or other clinical uses has not been established.   
 

Proudly made in the USA! Click here for more made in America products!


PR1MA™ Cod Uracil-DNA Glycosylase

 

PR1MA™ Cod Uracil-DNA Glycosylase (cUNG) is a recombinant, thermolabile enzyme that removes uracil from DNA. It is ideal for preventing carry over contamination during RNA or DNA amplification reactions that substitute dUTP for dTTP. cUNG is the only commercially available UNG that is completely and irreversibly inactivated by moderate heat treatment, unlike bacterial versions of the enzyme. Cod UNG treatment in combination with targeted pre-amplification using dUTP provides a simple and efficient solution to eliminate carry-over contamination and the generation of false positives and inaccurate quantification.

  • Optimal temperature: 37°C
  • Heat inactivation: 55°C for 5 minutes
  • Enables contamination control in PCR and other amplification methods
  • Does not degrade product after inactivation, enabling downstream use of the amplicon
  • Storage temperature: -20°C

Buffer composition

  • 50% glycerol
  • 50 mM Tris-HCl
  • 50 mM KCl
  • 1 mM DTT
  • 0.1  mM EDTA
  • 0.1% Tween-20
  • pH = 7.5

*These products are intended for research use only, not for therapeutic or diagnostic purposes in humans or animals. The safety and efficacy of these products in diagnostic or other clinical uses has not been established.
 

Proudly made in the USA! Click here for more made in America products!   


PR1MA™ Reverse Transcriptase, RNase H -

 

PR1MA™ reverse transcriptase (RT) is an RNA-dependent DNA polymerase ideal for use in RT-PCR and first-strand synthesis of complementary DNA (cDNA) for generation of cDNA libraries from single-stranded RNA, DNA, or RNA:DNA hybrids.

  • Decreased RNase H activity enables longer cDNA synthesis (>5 kb).
  • Lacks 3’ to 5’ exonuclease activity
  • Optimal temperature at 42°C
  • Temperature range: 40 to 50°C
  • Heat inactivation: 70°C for 20 minutes
  • Storage temperature: -20°C
  • 10X reaction buffer included 

Buffer composition

  • 50% glycerol
  • 50 mM Tris-HCl
  • 50 mM KCl
  • 1 mM DTT
  • 0.1  mM EDTA
  • pH = 7.5

*These products are intended for research use only, not for therapeutic or diagnostic purposes in humans or animals. The safety and efficacy of these products in diagnostic or other clinical uses has not been established.

 

Proudly made in the USA! Click here for more made in America products!


PR1MA™ MS2 Phage

 

PR1MA™ MS2 is an E. coli bacteriophage with a single-stranded RNA genome of 3569 nucleotides protected from nuclease degradation by a capsid of 180 coat protein monomers. This virus is a Biosafety Level 1 organism, not pathogenic to humans. These properties make MS2 phage useful as a process control in nucleic acid-based amplification techniques like RT-PCR, RT-LAMP, particularly those that involve viral RNA extraction.

  • Biosafety level 1
  • Lysis: 65°C for 20 minutes or by standard RNA extraction
  • Storage temperature: 4°C 

Buffer composition

  • 10 mM Tris-HCl
  • 0.1  mM EDTA
  • pH = 8.0 

*These products are intended for research use only, not for therapeutic or diagnostic purposes in humans or animals. The safety and efficacy of these products in diagnostic or other clinical uses has not been established.
 

Proudly made in the USA! Click here for more made in America products!

PR1MA™ RNA Controls

 

Looking for safe assay controls for highly infectious viruses or foreign animal diseases?

 

MIDSCI™ offers a selection of PR1MA™ RNAs – nuclease-resistant, single-stranded RNAs, suitable as process controls for RNA extraction from various sample matrices. These specially engineered, non-infectious, MS2 phage-like particles protect their contents from degradation by nucleases and can package sequences of up to 1.5 kb from viruses such as SARS-CoV-2, foot-and-mouth disease virus, and human immunodeficiency virus.
 

Amount: Between 1E6 or 1E10 copies (cp)
Concentration: Between 1E7 or 1E10 cp / mL, respectively
Volume: 0.1 and 1 mL respectively
Lysis: 65° C for 5 minutes in the RT step or by standard RNA extraction
Storage temperature: 4°C

 

Buffer composition

  • 10 mM Tris HCl
  • 100 mM NaCl
  • 1 mM MgCl2
  • 0.1% gelatin
  • pH = 7.0 

*These products are intended for research use only, not for therapeutic or diagnostic purposes in humans or animals. The safety and efficacy of these products in diagnostic or other clinical uses has not been established.

 

Proudly made in the USA! Click here for more made in America products!


PR1MA™ RNase Inhibitor

 

PR1MA™ RNase Inhibitor (RI) is a 50 kDa protein that specifically inhibits RNases A, B, and C by binding noncovalently in a 1:1 ratio at high affinity. It can be used in isothermal amplification and molecular diagnostic assays, cDNA synthesis, and other applications where RNA stability is important. It is ineffective against RNase1, T1, S1 Nuclease, or RNase H. It has no inhibition of polymerase activity when used with Taq DNA polymerase, AMV, M-MuLV, HIV reverse transcriptases, or phage RNA polymerases.

 

Storage Buffer

  • 50% glycerol
  • 10 mM Tris-HCl
  • 50 mM KCl
  • 8 mM DTT
  • pH = 7.5 

*To prevent the release of ribonuclease from RNase Inhibitor, temperatures greater than 50°C and high concentrations of denaturing reagents such as urea should be avoided.

 

*These products are intended for research use only, not for therapeutic or diagnostic purposes in humans or animals. The safety and efficacy of these products in diagnostic or other clinical uses has not been established.

 

Proudly made in the USA! Click here for more made in America products!


PR1MA™ Taq DNA Polymerase 1X Master Mix

 

PR1MA™ DNA polymerase 1X Master Mix saves time and cost by enabling direct PCR amplification of unpurified templates. It contains a recombinant, truncated (lacks 5’ to 3’ exonuclease activity), highly thermostable DNA polymerase from the thermophilic bacterium Thermus aquaticus. The enzyme is thermostable up to 98°C for polymerase chain reaction assays and is provided as a complete reaction master mix consisting of reaction buffer, dNTPs, MgCl2, and loading dye and only requires the addition of primers and DNA template. Once PCR is complete, the reaction products can be loaded directly into an agarose gel for analysis.

  • Lacks exonuclease activity
  • Thermotolerant up to 98°C
  • Inhibitor Resistant
  • Ideal for colony PCR, genotyping, and GC-rich templates
  • Storage temperature: -20°C 

Important note: Please be sure to use the buffer provided with this product to ensure optimal results.

 

*These products are intended for research use only, not for therapeutic or diagnostic purposes in humans or animals. The safety and efficacy of these products in diagnostic or other clinical uses has not been established.

 

Proudly made in the USA! Click here for more made in America products!

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