PMA Enhancer for Gram Negative Bacteria, 5X Solution
Référence 31038
Conditionnement : 16ML
Marque : Biotium
PMA Enhancer for Gram Negative Bacteria, 5X Solution
This product improves PMA- and PMAxx™-mediated discrimination between live and dead gram-negative bacteria when performing viability PCR.

Viability PCR dyes like PMAxx™ or PMA are membrane-impermeant, which makes them dead cell specific. Once inside of a dead cell, they bind to DNA. Exposure to intense visible light renders the dyes reactive, and causes them to covalently attach to the DNA. This DNA modification prevents amplification in subsequent PCR reactions.
The basic v-PCR workflow involves the following 5 steps: dye addition, incubation, light exposure, DNA extraction, and qPCR.Product Description
PMA Enhancer for Gram Negative Bacteria improves PMA- and PMAxx™-mediated discrimination between live and dead gram-negative bacteria.
- Used in viability PCR with PMA or PMAxx™
- Decreases dead cell signal in gram-negative bacteria
- Should not be used with gram-positive bacteria
- Provided as a 5X solution
The mechanism by which Enhancer improves live/dead discrimination has not been determined. It may improve passive permeability of dead cell walls or membranes to the dye, and/or improve access of the dye to the dead cell DNA.
Viability PCR
Viability PCR is a powerful technology for the sensitive and rapid detection of viable microorganisms. Unlike time-consuming culturing methods, qPCR is a fast and sensitive method of detection. However, normal qPCR does not distinguish between live and dead cells. With v-PCR using PMAxx™ or PMA, you get the speed, sensitivity and specificity of PCR, plus quantifiable viability. And because no culturing is required, you can even detect viable but not culturable (VBNC) bacteria. The v-PCR technology can be applied not only to bacteria but to other organisms like yeast, viruses, eukaryotes, and archaea.
To learn more about the advantages of determining microbial or cell viability using viability PCR, visit the Viability PCR Technology Page.

E. coli were killed with mild heat treatment (56°C for 3 hrs) and treated with PMAxx™ or PMAxx™ + Enhancer, followed by light exposure using PMA-Lite™, DNA purification, and qPCR with Fast EvaGreen® qPCR Master Mix. dCt values were calculated by subtracting the Ct without dye from the Ct with dye. Only dead cells treated with PMAxx™ + Enhancer showed a large dCt, indicating that the dye successfully inhibited PCR of dead cell DNA.
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Request the Certificate of AnalysisReferences
Download list of curated PMA and PMAxx™ References and a list of PMA and PMAxx™ Validated Bacterial Strains.
Citations
Download list of curated PMA and PMAxx™ References and a list of PMA and PMAxx™ Validated Bacterial Strains.


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