Taq II Polymerase and PCR Master Mix
Superior Performance on Fidelity, Stability and Specificity.
Taq II polymerase is an enhanced Taq DNA polymerase optimised for routine PCR applications. The enzyme provides a higher sensitivity, yields and longer PCR amplification as compared to conventional Taq DNA polymerase. It is supplied with optimised Taq II Polymerase 10X buffer and 25mM MgCl2, minimising the need for optimisation.
Highlights
- Robust amplification
- Higher sensitivity as compared to conventional Taq
- Amplification of targets up to 6kb from genomic DNA
- High efficiency and PCR yields
- Fast – developed to work under fast thermal cycling conditions
Polymerase for everyday applications
- DNA sequencing
- DNA labelling
- PCR for cloning
- PCR amplification of DNA fragments up to 6kb
- Routine PCR
Specifications
Fidelity | 1X |
Amplification length | Up to 6 kb |
Overhang | Sticky ends/ 3'-A |
Polymerase | Taq II DNA polymerase |
Amplification speed | 30s-60s/kb |
Robust and efficient amplification
Better Sensitivity
Faster processivity
REDiant II DNA Polymerase & Master Mix
Formulated with Density Reagents and Inert Tracking Dyes to Enable Easy Visual Control
REDiant II Polymerase and PCR Mastermix uses the enhanced Taq II polymerase and are formulated with density reagents and inert tracking dyes to enable easy visual control during PCR set-up and direct loading of the reaction product into the gel. REDiant II PCR Master Mix is a premixed, ready to use solution which contains Taq DNA polymerase, dNTPs, MgCl2 and reaction buffer for amplification of DNA templates by PCR. This pre-mixed formulation saves time and reduces contamination by reducing the number of pipetting steps required for usual PCR set up. The mix is optimised for efficient and reproducible PCR. It also includes a red, inert tracking dye which migrates at the same rate as 1kb DNA fragment in a 1% agarose gel.
Highlights
- Direct loading of PCR products onto agarose gel without addition of gel loading buffer
- Visualizes the addition of polymerase into the PCR reaction mix and ensure complete mixing
- Acts as tracking dye in gel electrophoresis
- Red inert dye does not inhibit PCR
Polymerase for everyday applications
- DNA sequencing
- DNA labelling
- PCR for cloning
- PCR amplification of DNA fragments up to 6kb
- Routine PCR
Specifications
Fidelity | 1X |
Amplification length | Up to 6 kb |
Overhang | Sticky ends/ 3'-A |
Polymerase | Taq II DNA polymerase |
Reaction speed | 30s-60s/kb |
Robust and efficient amplification
Higher Sensitivity
Faster Processivity
Convenient & Ease of Handling
REDiant II contains red tracking dye to save time and prevent cross contamination between samples. The red tracking dye does not interfere with the PCR and serves as a loading dye for gel electrophoresis to monitor the progress of a running gel. The dye migrates at similar rate to a 500bp-800bp DNA fragment in a 1% agarose gel.
exTEN II PCR Master Mix
exTENsively Amplifies Up to 10kb
exTEN II is an unique premixed blend of Taq DNA polymerase, a proof-reading enzyme, dNTPs, MgCl2 and reaction buffer for amplification of DNA templates by PCR With the addition of a 3’ 5’ exonuclease (proof-reading) ability, the amplification efficiency is enhanced through a lower rate misincorporated nucleotides compared to just Taq DNA Polymerase alone.
exTEN II PCR Master Mix produces higher yields and amplifies longer fragments up to 10kb. Most of the amplified DNA fragments have 3’A overhang, while a small percentage are blunt-end. This premix formulation saves times and reduces contamination by reducing the number of pipetting steps for PCR setup. exTEN II PCR Master Mix consists of a density reagent and 2 tracking dyes which migrates at the same rate as a 4000bp and 50bp DNA fragment in a 1% agarose gel.
Highlights
- Superior yield and robust amplification of DNA fragments up to 10kb
- Greater sensitivity achieved with low concentration template DNA
- Minimum pipetting steps required as it is formulated for easy preparation and direct loading which also reduces contamination & errors
Specification
Fidelity | 1X |
Amplification length | Up to 10 kb |
Overhang | Mix of sticky & blunt ends |
Polymerase | Taq II DNA polymerase & proof-reading enzyme |
Amplification speed | 30s-60s/kb |
Superior Yield & Robust Amplification of DNA Fragments Up to 10kb
Better Sensitivity Achieved even in Low Concentration of DNA Template
Superior Performance
Convenient & Ease of Handling
Contact Us for Orders or Enquiries
Select Your Country
Product Review Form
Thank you for helping 1st BASE gather feedback on our products as we strive to work towards providing the best for our customers.
We look forward to reading your review and seeing your results!
Terms and Conditions apply.
- All product reviews submitted through this form will be reviewed and subjected to approval.
- 1st BASE reserves the right to change these terms and conditions at any time without prior notice.