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qPCR and qRT-PCR

qPCR and qRT-PCR: qPCR reagents & kits

qPCR reagents & kits

 

ntact Genomics (IG®, ig®) develops and manufactures high-quality enzymes, master mixes, and kits for conventional PCR, high-fidelity PCR, quantitative PCR (qPCR), genotyping, direct PCR, and nucleic acid sample preparation.

Our portfolio includes dye-based and probe-based qPCR master mixes, high-fidelity DNA polymerases, Taq and hot-start Taq formulations, ready-to-use PCR master mixes, Exonuclease I, and FastAmp® sample-preparation and direct-PCR solutions. These products are designed to deliver reliable amplification, high sensitivity and specificity, consistent performance, and convenient workflows across a broad range of research and molecular-testing applications.

Why Choose IG® PCR and qPCR Products?

  • Reliable Performance – Optimized for consistent amplification, sensitivity, specificity, and reproducibility.
  • Solutions for Diverse Applications – Products for routine PCR, high-fidelity amplification, qPCR, genotyping, direct PCR, and post-PCR primer cleanup.
  • Convenient Formats – Choose individual enzymes or ready-to-use master mixes to simplify setup and reduce pipetting errors.
  • Streamlined Sample Preparation – FastAmp® solutions enable rapid sample lysis and direct amplification without conventional DNA or RNA purification.
  • Consistent Quality – Manufactured under an ISO 13485:2016-certified quality management system.
  • Flexible Supply Options – Bulk quantities, custom formulations, private-label products, and OEM partnerships are available upon request.

Explore our PCR and qPCR product portfolio(opens in new tab) to select the right enzyme, master mix, or kit for your application.

Product Links

Size Available

Application & Benefits

IG® Green qPCR 2X Master Mix

200, 500 or 2,000 Reactions

Ready-to-use qPCR cocktail containing all components except primers and template.

igScript™ Probe-Based qPCR Master Mix

500, 1000, or 2,500 Reactions

Provides improved PCR efficiency, wider dynamic range, superior sensitivity, and specificity.

i7® High-Fidelity DNA Polymerase

200 or 500 Units

High fidelity, sensitivity, and processivity with an error rate approximately 280× lower than Taq DNA Polymerase.

i7® High-Fidelity DNA Polymerase 2X Master Mix

100 or 500 Reactions

Convenient master mix format of our high-fidelity polymerase.

Pfu 2X Master Mix

200 Reactions

Affordable and robust high-fidelity polymerase.

Taq DNA Polymerase

1,000 or 5,000 Units

For robust and affordable PCR.

Taq DNA Polymerase 2X Premix

500 or 1,000 Reactions

Convenient master mix format of our robust Taq DNA Polymerase.

Hot Start Taq 2X Master Mix

500 Reactions

Reduces non-specific amplification during setup and improves PCR specificity and sensitivity.

Exonuclease I (Exo I)(opens in new tab)

5,000 Units or 20,000 Units

Removes residual primers while preserving dsDNA.

FastAmp® Plant Direct PCR Kit

250 or 1,250 Reactions

Amplifies DNA directly from plant samples without DNA purification.

FastAmp® Plant Direct PCR & Genotyping Solution

20 mL

Rapid cell lysis and DNA separation without the need for DNA extraction.

FastAmp® Viral and Cell Lysis Solution

100 Reactions (50 mL) or 500 Reactions (250 mL)

Streamlines sample collection, storage, and amplification by isothermal RPA.

 


Glycerol-free Reverse Transcriptase

igScript™ Glycerol-free Reverse Transcriptase is a recombinant Moloney Murine Leukemia Virus (MMLV) reverse transcriptase with reduced RNase H activity. It is highly efficient at producing full-length cDNA from long RNA templates. igScript™ Glycerol-Free Reverse Transcriptase enables reliable cDNA synthesis and is ideal for lyophilized RT-PCR, RT-qPCR, and molecular diagnostic assays.

Intact Genomics

Catalogue No.DescriptionPack SizePriceQty
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IG-3342GFGlycerol-free Reverse Transcriptase10,000 units (200 u/µl) �229.67 Quantity
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IG-3344GFGlycerol-free Reverse Transcriptase 50,000 units (200 u/µl) �448.63 Quantity
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igScript™ Glycerol-free Reverse Transcriptase is a recombinant Moloney Murine Leukemia Virus (MMLV) reverse transcriptase with reduced RNase H activity. It is highly efficient at producing full-length cDNA from long RNA templates. igScript RT is an RNA-directed DNA polymerase which lacks 3´ → 5´ exonuclease activity and is capable of producing cDNA from as little as 50 pg of total RNA for real-time RT-PCR analysis and other applications.

Protein Purity:

The physical purity of this enzyme is ≥98% as assessed by SDS-PAGE with Coomassie® blue staining (see figure below).

Product Source

The gene encoding recombinant MMLV Reverse Transcriptase with mutated RNase H domain is expressed in E. coli.

Applications

  • First strand cDNA synthesis for PCR or RT-PCR
  • Gene expression data validation by using RT-PCR

Benefits

  • Recombinant MMLV reverse transcriptase with greatly reduced RNase H activity.
  • Active at temperatures up to 55°C.
  • Highly efficient at producing full-length cDNA from as little as 50 pg of total RNA.

Product Includes

  1. igScript™ Reverse Transcriptase
  2. 10x igScript™ RT Reaction Buffer

Storage Temperature
–20 °C

1X MMLV Reverse Transcriptase Reaction Buffer
50 mM Tris-HCl, 75 mM KCl, 3 mM MgCl2, 10 mM DTT, pH 8.3 @ 25°C

Storage Buffer
50 mM Tris-HCl, 50 mM KCl, 1 mM DTT, 0.1 mM EDTA, 50% Glycerol, pH 7.5 @ 25ºC

Unit Definition
One unit is defined as the amount of enzyme required to incorporate 1 nmol of dTTP into acid insoluble material in 10 minutes at 37 °C using poly r(A)/oligo (dT) as a substrate.

Heat Inactivation
65°C for 20 minutes.

If you cannot find the answer to your problem then please contact us or telephone +44 (0)1954 210 200

First Strand cDNA Synthesis Protocol

1. In a sterile micro-centrifuge tube, add the following components on ice: reverse-transcriptase-pic2.

2. Heat the reaction for 5 minutes at 65 °C. Spin down briefly.

3. Place the tube immediately on ice. Add the following components: reverse-transcriptase-pic3.

4. If using random hexamers, incubate the reaction at 25 °C for 10 minutes, then proceed to step

5. Incubate the reaction at 42 °C for 30–60 minutes.

6. Inactivate the enzyme by incubating at 65 °C for 20 minutes.

7. Store products at -20 °C or proceed to the next step.

* RNase inhibitor can be purchased from any commercial source

If you cannot find the answer to your problem then please contact us or telephone +44 (0)1954 210 200

If you cannot find the answer to your problem then please contact us or telephone +44 (0)1954 210 200