Venor®GeM qEP

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Venor®GeM qEP utilizes quantitative, real-time PCR (qPCR) for fast (ca. 3 h) and reliable screening of cell culture supernatants for mycoplasma contaminations. The kit can be used in combination with any type of real-time PCR cycler able to detect the fluorescence dyes FAM™ and HEX™.
All Mollicutes (Mycoplasma, Acholeplasma, Spiroplasma) species so far described as contaminants of cell cultures and media components are specifically detected by amplifying a highly conserved rRNA operon, or more specifically, the 16S rRNA coding region in the mycoplasma genome. The mycoplasma-specific amplification is detected at 520 nm (FAM™ channel). False negative results due to PCR inhibitors or improper DNA extraction can be ruled out by using the provided internal amplification control, which is detected at 610 nm (HEX™ channel).

Type of PCR

TaqMan® based qPCR Assay with FAM™ and HEX™ labeled probes

Recommended Use

Venor®GeM qEP is used for direct detection of Mollicutes (Mycoplasma, Acholeplasma, Spiroplasma) contamination in cell cultures and cell media components.

Kit Components

Lyophilized Mix: Primer sets / Nucleotides / Probes / Polymerase in aliquots of 25 reactions each
Rehydration Buffer
Lyophilized Internal Control DNA
Lyophilized Positive Control
PCR Grade Water

Package Sizes
  • Cat. No. 11-9025 25 reactions
    Cat. No. 11-9100 100 reactions
    Cat. No. 11-9250 250 reactions
Result Evaluation

Cycler based, real-time PCR

Required Consumables

PCR reaction tubes
Optional for process validation and EP 2.6.7 / JP G3 compliant testing:
Internal Control DNA extra (4 vials for 300 µl each of Internal Control DNA; Cat. No. 11-9905)
10CFU™ Sensitivity Standards available for all EP 2.6.7 / JP G3 listed mycoplasma species

Required Lab Devices

qPCR cycler with FAM™ and HEX™ filter
Pipetting equipment
Benchtop centrifuge for 1.5 ml reaction tubes

Shelf Life and Storage

Components can be stored at +2 to +8 °C for at least 12 months. After rehydration the reagents must be stored at ≤ -18 °C.

EP 2.6.7 / JP G3 Compliance


Please note that validation data are provided for information purpose only. EP 2.6.7 clearly states “Where commercial kits are used …, documented validation points already covered by the kit manufacturer can replace validation by the user. Nevertheless, the performance of the kit with respect to its intended use has to be demonstrated by the user (e.g. detection limit, robustness, cross-detection of other classes of bacteria.”. Please feel free to contact us if you need further assistance.


Fig. Amplified dilution series of Mycoplasma fermentans, performed on a Corbett RotorGene®6000.