PMA Real-Time PCR Bacterial Viability Kit – Listeria monocytogenes (hly)

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Product Description

PMA-PCR kits are designed for selective detection of viable bacteria from a specific strain using PMA or PMAxx dye and real-time PCR. The kits contain PMA or PMAxx dye, Fast EvaGreen qPCR Master Mix, and PCR primers for detection of selected strains of bacteria that are of widespread interest to food safety, public health, and/or antibacterial research.

This kit contains primers for amplification of Listeria monocytogenes hly gene, with reagents sufficient to treat 80 bacterial cultures with PMA or PMAxx, and perform 200 PCR reactions. There is an option to choose either PMA or PMAxx for the viability dye (see below for more information about these dyes). The number of samples that can be treated with PMA or PMAxx using the kit may vary depending on sample type. See the product protocol under the downloads tab and references for more information.

Kit contents:

PMA™ is a high affinity photoreactive DNA binding dye developed by Biotium. The dye is weakly fluorescent by itself but becomes highly fluorescent upon binding to nucleic acids. It preferentially binds to dsDNA with high affinity. Upon photolysis, the photoreactive azido group on the dye is converted to a highly reactive nitrene radical, which readily reacts with any hydrocarbon moiety at the binding site to form a stable covalent nitrogen-carbon bond, thus resulting in permanent DNA modification. The dye is cell membrane-impermeable and thus can be used to selectively modify DNA from dead cells with compromised membrane integrity, while leaving DNA from viable cells intact. PMA inhibits PCR amplification of modified DNA templates by a combination of removal of modified DNA during purification and inhibition of template amplification by DNA polymerases (see Reference 1 under the references tab). Consequently the dye is useful in the selective detection of viable pathogenic cells by quantitative real-time PCR.

PMAxx™ is a new and improved version of PMA designed by Biotium scientists to be a superior alternative to PMA. While PMA is generally effective at differentiating between live and dead bacteria by qPCR, it does not completely eliminate PCR products from dead cell DNA. This could potentially give false positive results. Biotium’s new dye PMAxx is much more effective at eliminating PCR amplification of dead cell DNA, and therefore provides the best discrimination between live and dead bacteria.

Fast EvaGreen® Master Mix is a ready-to-use hot-start mix for qPCR and DNA melt curve analysis of PCR amplicons. It is formulated for qPCR using a fast cycling protocol, but also can be used for qPCR using regular cycling protocols. EvaGreen dye is a unique DNA-binding dye with features ideal for both qPCR and melt curve analysis. EvaGreen dye binds to dsDNA via a novel “release-on-demand” mechanism, which permits the use of a relatively high dye concentration in qPCR without PCR inhibition. Fast EvaGreen Master Mix contains Cheetah™ Taq, Biotium’s fast-activating chemically-modified hot-start Taq polymerase, which is particularly suitable for fast PCR cycling protocols.

Listeria monocytogenes is a food-borne pathogen that can cause digestive illness and fetal harm. The gene hly encodes the Listeria Lysin O (LLO) protein that is specific for Listeria. PMA-PCR using these primers for viability PCR in Listeria has been published (see Reference 2 under the references tab). In addition, these primers have been validated at Biotium for real-time qPCR using EvaGreen Master Mix (see product protocol under downloads for details).

Also see our other PMA-PCR kits for detection of Staphylococcus aureus, methicillin-resistant Staphylococcus aureus (MRSA), E. coli, E. coli O157:H7Mycobacterium tuberculosis, Legionella pneumophila, and Salmonella enterica. Don’t see your favorite strain? Let us know at techsupport@biotium.com.

Materials from Biotium are sold for research use only.

1. Nocker A, et al. Comparison of propidium monoazide with ethidium monoazide for differentiation of live vs. dead bacteria by selective removal of DNA from dead cells. J. Microbiol. Meth. 67(2), 310-320 (2006).

2. Nocker A, et al. Molecular monitoring of disinfection efficacy using propidium monoazide in combination with quantitative PCR. J. Microbiol. Meth. 70(2), 252-260 (2007).

3. Fittipaldi M, et al. Progress in understanding preferential detection of live cells using viability dyes in combination with DNA amplification. J. Microbiol. Meth. 91(2), 276-289 (2012).

Download the PMA reference list

Additional Information

Viability dye

PMA, PMAxx

Flyer (PDF): FL-PMA-and-PMAxx-2015

MSDS (PDF): MSDS 31051

Protocol (PDF): PI-31051-31051-X

Shipment Method: Shipping and handling methods will be assessed and calculated at time of shipment based upon item(s) storage temperature conditions.

Expedited shipment may be requested at time of checkout.

Please note that products with recommended storage at 4°C or -20°C may ship at ambient temperature. This will not affect product performance. When you receive the product, place it under the recommended storage conditions.

More information about product handling and shelf life