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Home > Site Map > Product List G > green taq polymerase
    14 products and services found for "green taq polymerase"
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  • Fast return: 4 days for ligation subcloning and additional 4 days if PCR is required;
    The insert and vector sizes do not matter;
    Various DNA templates;
    Vectors which you want to subclone DNA fragments into.

  • Fast return: 8 days for standard site-directed mutagenesis;
    Point mutations, deletions, or insertions of several amino acids can be performed in a single mutagenesis reaction. The same price is charged for incorporating several mutations, as long as the changes are localized and can be introduced in a single reaction. The same price is charged no matter the size of gene is.

  • Random mutagenesis based on PCR and other methods.

  • 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.

  • MB038-4G: 4G One-step RT-PCR Kit

    MB038-4Gb: 4G One-step RT-PCR Kit with blue dye

    The kit is provided in a convenient Master Mix format. The 2 x One-step Mix contains optimized buffer system, dNTP and loading dye; One-step Enzyme Mix contains optimized ratio of 4G Reverse Transcriptase, Murine RNase inhibitor, and hot start Taq DNA polymerase.

    * High efficiency. Integrating the superior performance of 4G Reverse Transcriptase and hot-start Taq DNA Polymerase, with an optimized buffer system, the detection sensitivity of the 4G One Step RT-PCR Kit can reach 1 pg total RNA and can be amplified Fragments up to 10 kb.
    * High purity. >98% homogeneous of the Taq DNA polymerase by SDS gel electrophoresis. No contamination detected in standard PCR test reactions.
    * Reproducible results.
    * Reverse transcription and PCR reactions are completed in one tube, no additional tube opening/pipetting operations are required, which improves detection throughput and reduces the risk of contamination.

  • MB127-5G: 5G RT Supermix for qPCR with gDNA Elimination Function

    * The 5G RT supermix for qPCR with gDNA elimination function is suitable for two-step RT-qPCR detection, and compatible with dye-based and probe-based qPCR, enabling high-performance gene expression analysis.
    * Simple and fast operation: one-step genome clearance and reverse transcription.
    * Higher reverse transcription efficiency and higher cDNA yields from all regions of RNA transcripts: based on the more efficient 5G Reverse Transcriptase.
    * Flexible choice of primers: Different types of reverse transcription primers can be used flexibly for different experimental designs.
    * Excellent cDNA stability: complete deactivation of thermal DNase and long-term storage of cDNA.
     

    MB127-4G: 4G RT Supermix for qPCR with gDNA Elimination Function

    * The 4G RT supermix for qPCR with gDNA elimination function is suitable for two-step RT-qPCR detection, and compatible with dye-based and probe-based qPCR, enabling high-performance gene expression analysis.
    * Based on the highly efficient 4G Reverse Transcriptase, the super temperature tolerance ensures that the complex secondary structure of RNA can be opened under high temperature conditions to obtain longer cDNA.
    * Quick and complete removal of genome contamination by the 4 × gDNA Removing Buffer: to ensure more reliable follow-up results, and simplify the design of qPCR primers, without the need to design primers across introns.
    * Different primers are selected for different downstream applications.

  • MB040-HY2: 2x HY PCR Master Mix, with blue dye

    * The PCR master mix simplifies the assembly of PCR reaction and offers advantages of time savings, convenience, consistency, and minimal risk of contamination and pipetting errors.
    * The high yield PCR Master Mix has increased amplification robustness, fidelity, yield, and fragment length, as well as the ability to handle difficult or “dirty” templates.
    * The tracking dye and precipitant have been added into the PCR PreMix so that the PCR product can be directly loaded for electrophoresis.

    Features of the blend of Taq enzyme and a proofreading enzyme contained in the high yield PCR master mix:
    * 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 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.

  • MB041-EN-1: dNTP Mix, 10 mM each

    Chemically synthesized and >99% purity confirmed by HPLC;
    Free of human and E. coli DNA;
    Free of DNases and RNases;
    Free from PCR, qPCR, and cDNA synthesis inhibitors;
    Stable for 2 years at –20°C.

  • MB067-EQ2G / MB067-EQ2B: 2x PCR PreMix, with dye (green, or blue)

    * The PCR master mix simplifies the assembly of PCR reaction and offers advantages of time savings, convenience, consistency, and minimal risk of contamination and pipetting errors.
    * The tracking dye and precipitant have been added into the PreMix so that the PCR product can be directly loaded for electrophoresis.

    Features of the Taq DNA polymerases contained in the PCR master mix:
    * 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.

  • 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.

About our green taq polymerase products
14 green taq polymerase products are offered for sale on sydlabs.com, and welcome to contact us if you are interested in more green taq polymerase related products, which may be under development and close to be listed for sale. We have always tried our best to reduce cost to offer the cheapest green taq polymerase products.
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