NEB offers a wide range of DNA polymerases and through our commitment to research, ensures the development of innovative and high quality tools for PCR related applications. In addition, our collaboration with Finnyzmes Oy brings an unsurpassed offering of state-of-the-art products for PCR and qPCR combined with the service and quality for which NEB is known. Several factors influence the choice of an optimal enzyme for a specific PCR application. The following chart highlights the most significant properties to be considered when choosing a DNA polymerase for PCR.
| Fidelity vs Taq |
Optimal Extn Range |
Difficult Templates | Resulting DNA ends | 3´→ 5´ exo |
PCR Kit /Master Mix Available |
Units /50µ Rxns |
Advantages | |
|---|---|---|---|---|---|---|---|---|
| 1X |
≤ 3kb |
- |
3'A |
No |
No/No |
1.5-2.5 |
Taq with a colored buffer–load PCR product directly on a gel to track migration |
|
| Phire Hot Start DNA Polymerase(1) | 2X | ≤7.5kb | x | Blunt | Yes | No/No |
1.0 | Quick hot start (no reactivation step) High Speed (3X faster than Hot Start Taq) High Yield |
| 50X |
≤20kb |
xxx |
Blunt |
Yes |
Yes/Yes |
0.5-1.0 |
Extreme fidelity (50X greater than Taq) High speed (5X faster than Pfu) Robust reactions High yield Choice of formats and reaction buffers |
|
| 50X |
≤20kb |
xxx |
Blunt |
Yes |
No/No |
0.5-1.0 |
Extreme specificity Extreme fidelity (50X greater than Taq) High speed (5X faster than Pfu) Robust reactions High yield |
|
| 5X |
≤6kb |
xx |
Blunt |
Yes |
No/No |
0.2-1.0 |
High-fidelity (5X greater than Taq) Extremely high thermostability |
|
| 5X |
≤6kb |
x |
Blunt |
Yes |
No/No |
0.2-1.0 |
High-fidelity (5X greater than Taq) High thermostability (half-life of 6.7 hr at 95°C) |
|
| 2X |
≤40kb |
xxxx |
3´A & |
Yes |
Yes/No |
0.5-2.0 |
Amplifies up to 40 kb Ideal for GC-rich or looped sequences Robust reactions with standard templates |
|
| 1X |
≤3kb |
- |
3´A |
No |
No/No |
0.75-2.0 |
Minimizes non-specific amplification Room temperature reaction set up Able to incorporate dUTP, dITP and fluorescently-labeled nucleotides |
|
| 1X |
≤3kb |
- |
3´A |
No |
Yes/Yes |
0.5-2.0 |
Industry standard for routine PCR Choice of formats and reaction buffers to accomodate a variety of PCR applications Tolerates a wide range of templates Incorporates dUTP, dITP and flourescently-labeled nucleotides |
|
| 6X |
≤40kb |
xxxx |
3´A & Blunt |
Yes |
Yes/Yes |
5 |
Amplifies up to 40 kb from lambda DNA and up to 30 kb from human genomic DNA Tolerates a wide ramge of templates Robust reactions |
(1) Manufactured by Finnzymes Oy. distributed by New England Biolabs, Inc.
Taq DNA Polymerase is the industry standard for routine PCR, known for robust and reliable reactions. NEB provides high quality, recombinant Taq at exceptional value in terms of cost per unit. For your convenience, this versatile enzyme is now available in a variety of formats:
| Multiplex PCR 5X Master Mix | For 2 or more products in a single reaction |
| Crimson Taq DNA Polymerase | Load PCR product directly on a gel |
| Taq PCR Kit | Everything you need to perform 200 PCR reactions |
| Taq PCR Kit with Controls | Also includes 30 control reactions |
| Taq 2X Master Mix Taq 5X Master Mix |
Just add template and primers |
| Quick-Load Taq 2X Master Mix | Also includes dyes for tracking |
| Taq DNA Polymerase with ThermoPol Buffer | Uniquely formulated buffer for high product yields |
| Taq DNA Polymerase with ThermoPol II (Mg-free) Buffer | Additional Mg+2 control |
| Taq DNA Polymerase with Standard Taq Buffer | Detergent free buffer for high throughput applications |
| Taq DNA Polymerase with Standard Taq (Mg-free) Buffer | Additional Mg+2 control |
| Crimson Taq DNA Polymerase | Buffer contains density reagent for direct gel loading |
| Crimson Taq DNA Polymerase with Mg-Free Buffer | Mg-free Buffer contains density reagent for direct gel loading |