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    List Price*
    500 x 50µl Reactions
    538,00 €
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    BIO-X-ACT™ Short DNA Polymerase and BIO-X-ACT™ Short Mix will be discontinued in December 2018. We advise customers to upgrade to the new generation reagents MyFi™ DNA Polymerase and MyFi™ Mix respectively. Thank you

    BIO-X-ACT™ Short Mix is a complete, ready-to-use, 2x reaction mix that enables PCR assays to be performed on problematic templates through the simple addition of water, template and primers.

    Product Highlights

    • High performance - for templates that fail with standard Taq DNA Polymerases
    • For problematic templates - works with high GC content, dirty templates, or difficult melting profiles
    • Ideal for short amplicons - amplifies genomic fragments up to 3 kb
    • Convenient - pre-mixed, pre-optimized 2x solution
    • Ready to use - reduces risk of contamination

    Product Description

    BIO-X-ACT™ Short Mix is a complete, ready-to-use, 2x reaction mix which enables PCR assays on problematic templates, simply by adding water, template and primers.

    BIO-X-ACT Short is recommended for short genomic DNA fragments up to 3 kb and Lambda DNA up to 5 kb.

    To achieve optimal reaction conditions, the BIO-X-ACT Short Mix contains BIO-X-ACT™ Short DNA Polymerase, MgCl2, ultra-pure dNTPs manufactured by Bioline, as well as additives. The mix has been optimized for a wide variety of templates and an additional 50 mM MgCl2 solution is included, should fine-tuning be required.

    BIO-X-ACT Short Mix reduces the time needed to set up reactions, thereby minimizing the risk of contamination. Greater reproducibility is ensured through a reduction in the number of pipetting steps that can introduce errors.


    • Suitable for cloning
    • Short amplicons

    PCR Enzyme Guide

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    PCR Selection Chart

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    500 Reactions

    BIO-X-ACT Short Mix

    10 x 1.25 mL

    50 mM MgCl2 Solution

    1.2 mL


    • BIO-25026: 500 x 50 µL Reactions: 10 x 1.25 mL



    Storage & Stability

    All components are shipped on dry/blue ice and should be stored at -20°C upon receipt for optimum stability. Repeated freeze/thaw cycles should be avoided. When stored under the recommended conditions and handled correctly, full activity of the reagents is retained until the expiry date on the outer box label.

    Components may also be stored at +4°C if required, although storage at -20°C is recommended. When stored at +4°C, reagents will remain stable for a period of 2 weeks from date of receipt.


    Bioline's mixes contain magnesium chloride at the following concentrations (please see table below). An additional tube of 50 mM MgCl2 solution is supplied with each mix to facilitate further optimization if required.

     Bioline Mix Final Magnesium Concentration
    ACCUZYME Mix  2.0 mM.
    BioMix / BioMix Red  2.5 mM.
    ImmoMix / ImmoMix Red  3.0 mM.
    BIO-X-ACT Short Mix  2.0 mM.
    MangoMix  2.5 mM.
    MyTaq  3.0 mM.
    RANGER  1.5 mM.

    At Bioline we pride ourselves in supplying high-quality polymerases to suit your requirements. To aid your selection of the most suited enzyme for your specific applications, please see our enzyme selection tool.

    All our polymerases are guaranteed for a period of 12 months from the date of purchase. These should be stored at -20°C during this time for optimal retention of activity.

    Please Note: We do not recommend the storage of our polymerases at -80 °C as ice crystals could form on the active site, which may affect or destroy the activity of the enzyme.

    PCR can be a challenging technique, with various parameters to optimize to achieve the best results. If you are having problems, these could be easily resolved by addressing a few issues. Please see our PCR troubleshooting guide for suggestions and help with your specific problems.

    Observation Recommended Solution(s)
    No or low PCR yield  Enzyme concentration too low – increase the amount of enzyme in 0.5 U increments.
     Primers degraded – check quality and age of the primers.
     Magnesium concentration too low – increase concentration in 0.25 mM increments with a starting  concentration of 1.75 mM.
     Primer concentration not optimized. Titrate primer concentration (0.3-1 µM); ensuring that both  primers have the same concentration.
     Template concentration too low – Increase concentration of template.
     Perform a positive control to ensure that the enzyme, dNTPs and buffers are not degraded and/or contaminated.
    Multiple Bands  Primer annealing temperature too low. Increase annealing temperature. Primer annealing should be at least 5°C below the calculated Tm of primers.
     Prepare master mixes on ice or use a heat-activated polymerase.
     For problems with low specificity. Try adding 3% DMSO (not supplied) to improve specificity.
    Smearing or artifacts  Template concentration too high. Prepare serial dilutions of template.
     Too many cycles. Reduce the cycle number by 3-5 to remove non-specific bands.
     Enzyme concentration too high - decrease the amount of enzyme in 0.5 U increments.
     Extension time too long. Reduce extension time in 0.5-1 minute increments.

    These terms refer to parameters to be considered when performing PCR and are important features in selecting the correct enzyme for your needs. Understanding what they mean is therefore crucial: Yield: The amount of DNA produced in a PCR reaction. Fidelity: The accuracy of the enzyme at incorporating the correct dNTP to the elongating DNA strand. Processivity: The length of time a polymerase is associated with the template and therefore the size of fragment which can be amplified. Specificity: A measure of the unwanted by-products generated in a reaction.

    In nature, the ability of a DNA polymerase to correct misincorporations of nucleotides in the DNA strand being elongated is often crucial to the survival of the host organism. This ability is termed "proofreading activity" and occurs in the 3' to 5' direction. This activity also leads to the polymerase removing unpaired nucleotides overhanging at the 3'end (A-overhangs), creating blunt ends.

    One unit is defined as the amount of enzyme that incorporates 10 nmoles of dNTPs into acid-insoluble form in 30 minutes at 72°C.

    All Bioline polymerases are available in the convenient format of a 2x master mix, containing all the reagents and additives necessary to perform successful PCR, with the exception of template, primers and water. This formulation not only provides a convenient and hassle-free PCR setup, but also significantly reduces the chances of human error, inaccuracies and contamination by reducing the pipetting steps required.

    We recommend a final reaction volume of 50 µL, this requiring the use of 25 µL of the 2x master mix and to make up to 50 µL using template, primers and PCR grade water.

    Whilst the exact composition of the mixes is proprietary information, all mixes are made up of reaction buffer, magnesium, dNTPs, polymerase and additives, designed to keep the polymerase stable in the mix, as well as provide the optimal conditions for PCR.

    All Bioline PCR mixes come supplied at a 2x concentration, requiring the user simply to add template, primers and PCR grade water to a final concentration of 1x.