Need bulk, customized or optimized products for commercial purposes? We also offer support with logistics, compliance and more. Reach out to cooperate with QIAGEN Strategic Partnerships & OEM
VeraSeq PCR Mix (2x, 250 reactions)
Cat. No. / ID: P7610L
250 reactions (evaluation pack) of 2x VeraSeq PCR Mix (1 x 6.25 mL)
Log in To see your account pricing.
The VeraSeq PCR Mix (2x, 250 reactions) is intended for molecular biology applications. This product is not intended for the diagnosis, prevention, or treatment of a disease.
Certain applications in which this product can be used may be covered by patents issued and applicable in the United States and abroad. Purchase of this product does not include a license to perform any patented application; therefore, it is the sole responsibility of the users of the product to determine whether they may be required to engage a license agreement depending upon the particular application in which the product is used.
Need bulk, customized or optimized products for commercial purposes? We also offer support with logistics, compliance and more. Reach out to cooperate with QIAGEN Strategic Partnerships & OEM
Features
- 2x master mix based on VeraSeq™ 2.0 (cat. no. P7511L)
- 50x greater fidelity than Taq DNA Polymerase
- Ultra-thermostable polymerase
- Extends 1 kb in 15 seconds
- Strong proofreading activity (3'→5' exonuclease activity)
Product Details
VeraSeq™ PCR Mix is a premixed, ready-to-use 2x solution containing VeraSeq™ 2.0 High-Fidelity DNA Polymerase (P7511L), dNTPS, MgCl2 and reaction buffer at optimal concentrations to maximize the speed, accuracy and length of DNA synthesis. The formulation provides efficient, high-fidelity DNA amplification, cloning and synthetic biology applications.
Performance
Polymerase properties
- Storage temperature: –25°C to –15°C
- Extension rate: 15 second per kb at 72˚C
- Proofreading (3'→5' exo): Yes, strong
- Nick-translation (5'→3' exo): No
- Fidelity: >50x higher than Taq DNA Polymerase
- Strand displacement: No
- Thermostability: Highly thermostable
- Able to extend an RNA primer: No
- Extends from a nick: No
- Generate blunt end products: Yes
- Uracil read through: No
| Test | Specification |
| Functional Assay | Amplification of 500 bp fragment from genomic DNA |
Principle
Source of recombinant enzyme protein
The protein is produced by a recombinant E. coli strain carrying the engineered VeraSeq™ 2.0 gene.
Unit definition
One unit is defined as the amount of enzyme required to incorporate 10 nmoles of dNTPs into acid-insoluble form at 74°C in 30 minutes.
Procedure
Protocol
General precautions should be taken when setting up a PCR, including setting up the reaction on ice, adding master mix last, gently pipetting, thorough mixing and a quick centrifugation. The following procedure can be used as a guideline. Reactions may need to be optimized individually.
Reaction setup (for 50 µL)
| Component | Volume (µL) | Final concentration |
| Sterile H2O | 20, variable | N/A |
| 2x VeraSeq PCR Mix | 25 | 1x |
| PCR Primer Cocktail | 5 | 0.5 µM each |
| Library DNA* | Variable | N/A |
* Total reaction volumes of library DNA and water should be adjusted to achieve a final reaction lolume of 50 µL. If the reaction volume needs to be >50 µL, the volume of the 2x Master Mix should be adjusted so that it constitutes 50% of the final reaction volume.
| Step | Temperature | Time | Cycles |
| Initial denaturation | 98°C | 30 seconds | 1 |
| Denaturation Annealing Extension |
98°C 60°C 72°C |
10 seconds 30 seconds 30 seconds |
To be determined by user† |
| Final extension | 72°C 4°C |
300 seconds hold |
1 |
* Cycling conditions may need to be optimized, depending on the amplicon of interest.
† Number of cycles is dependent on the amount of input DNA and other specific sequence analysis requirements.
Quality control analysis
Functionality of 2x VeraSeq™ PCR Mix is assessed by its ability to amplify a 500 bp fragment from genomic DNA. Following PCR the 500 bp fragment was visualized by agarose-gel electrophoresis.
Contamination Tests
VeraSeq™ PCR Mix was tested prior to assembly and found to be free of contaminating endonucleases. Enzyme purity was >99% as determined by SDS-PAGE and negligible E. coli genomic DNA contamination was confirmed by qPCR. Specific activity was verified pre and post dilution.
Applications
This product is available for molecular biology applications such as:
- High-fidelity DNA amplification
- Cloning
- Synthetic biology
Resources
Safety Data Sheets (1)
Certificates of Analysis (1)