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
Applicable in research and industry for the direct detection of Mollicutes (Mycoplasma, Acholeplasma, Spiroplasma) contaminations in cell cultures and biopharmaceuticals. Approved for testing according to EP 2.6.7 and JP G3.
Lyophilized Mix: Primer sets / Nucleotides/ Probes / Polymerase in aliquots of 25 reactions each
Lyophilized Internal Control DNA
Lyophilized Positive Control
PCR Grade Water
- Cat. No. 11-9025 25 Reactions
- Cat. No. 11-9100 100 Reactions
- Cat. No. 11-9250 250 Reactions
Cycler-based, real-time PCR
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 amplification control; 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
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