MB042-EUT: Taq DNA Polymerase
* High efficiency. The extension time of the Taq DNA polymerase is shorter than 30 seconds per kb DNA. Easily amplify DNA fragments up to 5 kb.
* High purity. >98% homogeneous of the Taq DNA polymerase by SDS gel electrophoresis. No contamination detected in standard PCR test reactions.
* Reproducible results. No visible activity change after storage of the Taq DNA polymerase at room temperature for 3 months to amplify a single-copy gene from human genome with high efficiency.
* Terminal transferase activity of adding a single nucleotide (adenosine) at 3' end of the extension product, facilitating TA cloning of PCR products.
* Low cost: 2.8+ cents per unit. The cheapest PCR enzyme in the market.MB087: Hot Start Taq DNA Polymerase
* High efficiency. The extension time of the Taq DNA polymerase is shorter than 30 seconds per kb DNA. Easily amplify DNA fragments up to 5 kb.
* High specificity.
* Reproducible results.
* Terminal transferase activity of adding a single nucleotide (adenosine) at 3' end of the extension product, facilitating TA cloning of PCR products.
* Low cost: $0.19+ per unit. The cheapest hot start Taq enzyme in the market.MB117: Hot Start Taq DNA Polymerase for Probe-based qPCR
* High amplification specificity and sensitivity for detection of low-copy genes paired with the most suitable buffer optimized for qPCR and PCR.
* For probe-based qPCR, excellent amplification curve within a wide quantitative range, and accurately quantify and detect target genes.
* Compatibility in terms of template type, template GC content, and primer Tm values.
* Good tolerance to impurities and is suitable for use in a variety of testing scenarios.
* Low cost: $0.19+ per unit. The cheapest hot start Taq enzyme in the market.MB118: Hot-Start High-Fidelity DNA Polymerase
* Long fragment amplification: up to 40 kb from simple templates such as λDNA and plasmids, up to 20 kb from complex templates such as genomic DNA, and up to 10 kb from cDNA templates.
* Fast amplification speed: normally ~30 sec/kb; ~0.5 sec/kb if the amplification length is <1 kb; 4-150 times that of conventional Taq DNA polymerase.
* High specificity: Its amplification mismatch rate is 1/53 that of ordinary Taq polymerase and 1/6 that of Pfu polymerase.
* Reproducible results: even with the GC-rich fragments and in the presence of PCR inhibitors.
* Blunt-ended amplified products.
* Low cost: $0.8 per unit. The cheapest hot start high fidelity Taq enzyme in the market.MB016-HYT: High Yield Taq DNA Polymerase
* Robust processivity. Up to 10 kb human genomic and 15 kb lamda DNA fragments have been tested for amplification.
* High purity. >98% homogeneous of the Taq DNA polymerase by SDS gel electrophoresis. No contamination detected in standard PCR test reactions.
* Reproducible results. No visible activity change after storage of the high yield Taq DNA polymerase at room temperature for 3 months to amplify a single-copy gene from human genome with high efficiency.
* Proofreading with 5′ exonuclease activity.MB121: Bst 2G DNA Polymerase, Large Fragment
* Rapid amplification of diverse templates.
* Higher amplification yield.
* Increased tolerance of inhibitors including salts.
* Improved thermostability of the enzyme.
* The cheapest Bst 2.0 DNA Polymerase, Large Fragment in the market.
MB122: Bst DNA Polymerase, Large Fragment
* Warm-start reaction system: The reaction process is completed by simply mixing all components at 60 - 65 ℃ for 30 - 60 minutes.
* Multiple options of reading results: The amplification products can be checked with gel electrophoresis, colorimetric methods, and fluorescence intensity methods.
* Potent amplification ability: The upgraded polymerase features strong 5´→3´ DNA polymerase activity and strong strand displacement activity.
* Perfect for assembling RT-LAMP kits: Compatible with various reverse transcriptases from Syd Labs and other commercial suppliers.