Trainings and events

Dear cell culture users,

We are happy to announce that the qPCR-based mycoplasma detection service will be offered again on the first Wednesday of every month starting from October, just as before.

Key features of our detection protocol include (https://labsupport.pages.ist.ac.at/mycoplasma-detection/):

• Real-time PCR technology for rapid quantitative and qualitative analysis with high sensitivity
• Multiplex primers and probes targeting conserved mycoplasma DNA sequences
• Internal controls to ensure assay accuracy and sample quality
• Direct use of culture supernatant, no DNA extraction required

Please find below the sample preparation instructions (also available online here: https://labsupport.pages.ist.ac.at/mycoplasma-detection-guidelines/)

1. Cultivate cells without antibiotics for at least one week.
2. Collect 100 µL of supernatant from a culture at 90-100% confluence (grown for 2-3 days in the same media).
3. Heat-inactivate the supernatant at 95°C for 5 minutes. Note: Samples are stable at 4°C for up to 1 week.
4. Deliver samples to the 4°C fridge at the Sunstone Building, 1st Floor (I23.01.038). Tubes should be clearly labeled with user initials, sample number, and date (e.g., FS01_1oct25, FS02_1oct25). Printed labels are preferred.
5. Create a PPMS order, this triggers an automated notification to us.

Pricing details are available here (login required): https://labsupport.pages.ist.ac.at/mycoplasma-detection-pricing-internal-rates/  and below:

Dear cell culture users,

We are happy to announce that the qPCR-based mycoplasma detection service will be offered again on the first Wednesday of every month starting from October, just as before.

Key features of our detection protocol include (https://labsupport.pages.ist.ac.at/mycoplasma-detection/):

• Real-time PCR technology for rapid quantitative and qualitative analysis with high sensitivity
• Multiplex primers and probes targeting conserved mycoplasma DNA sequences
• Internal controls to ensure assay accuracy and sample quality
• Direct use of culture supernatant, no DNA extraction required

Please find below the sample preparation instructions (also available online here: https://labsupport.pages.ist.ac.at/mycoplasma-detection-guidelines/)

1. Cultivate cells without antibiotics for at least one week.
2. Collect 100 µL of supernatant from a culture at 90-100% confluence (grown for 2-3 days in the same media).
3. Heat-inactivate the supernatant at 95°C for 5 minutes. Note: Samples are stable at 4°C for up to 1 week.
4. Deliver samples to the 4°C fridge at the Sunstone Building, 1st Floor (I23.01.038). Tubes should be clearly labeled with user initials, sample number, and date (e.g., FS01_1oct25, FS02_1oct25). Printed labels are preferred.
5. Create a PPMS order, this triggers an automated notification to us.

Pricing details are available here (login required): https://labsupport.pages.ist.ac.at/mycoplasma-detection-pricing-internal-rates/  and below:

Dear cell culture users,

We are happy to announce that the qPCR-based mycoplasma detection service will be offered again on the first Wednesday of every month starting from October, just as before.

Key features of our detection protocol include (https://labsupport.pages.ist.ac.at/mycoplasma-detection/):

• Real-time PCR technology for rapid quantitative and qualitative analysis with high sensitivity
• Multiplex primers and probes targeting conserved mycoplasma DNA sequences
• Internal controls to ensure assay accuracy and sample quality
• Direct use of culture supernatant, no DNA extraction required

Please find below the sample preparation instructions (also available online here: https://labsupport.pages.ist.ac.at/mycoplasma-detection-guidelines/)

1. Cultivate cells without antibiotics for at least one week.
2. Collect 100 µL of supernatant from a culture at 90-100% confluence (grown for 2-3 days in the same media).
3. Heat-inactivate the supernatant at 95°C for 5 minutes. Note: Samples are stable at 4°C for up to 1 week.
4. Deliver samples to the 4°C fridge at the Sunstone Building, 1st Floor (I23.01.038). Tubes should be clearly labeled with user initials, sample number, and date (e.g., FS01_1oct25, FS02_1oct25). Printed labels are preferred.
5. Create a PPMS order, this triggers an automated notification to us.

Pricing details are available here (login required): https://labsupport.pages.ist.ac.at/mycoplasma-detection-pricing-internal-rates/  and below:

Dear cell culture users,

We are happy to announce that the qPCR-based mycoplasma detection service will be offered again on the first Wednesday of every month starting from October, just as before.

Key features of our detection protocol include (https://labsupport.pages.ist.ac.at/mycoplasma-detection/):

• Real-time PCR technology for rapid quantitative and qualitative analysis with high sensitivity
• Multiplex primers and probes targeting conserved mycoplasma DNA sequences
• Internal controls to ensure assay accuracy and sample quality
• Direct use of culture supernatant, no DNA extraction required

Please find below the sample preparation instructions (also available online here: https://labsupport.pages.ist.ac.at/mycoplasma-detection-guidelines/)

1. Cultivate cells without antibiotics for at least one week.
2. Collect 100 µL of supernatant from a culture at 90-100% confluence (grown for 2-3 days in the same media).
3. Heat-inactivate the supernatant at 95°C for 5 minutes. Note: Samples are stable at 4°C for up to 1 week.
4. Deliver samples to the 4°C fridge at the Sunstone Building, 1st Floor (I23.01.038). Tubes should be clearly labeled with user initials, sample number, and date (e.g., FS01_1oct25, FS02_1oct25). Printed labels are preferred.
5. Create a PPMS order, this triggers an automated notification to us.

Pricing details are available here (login required): https://labsupport.pages.ist.ac.at/mycoplasma-detection-pricing-internal-rates/  and below:

Dear cell culture users,

We are happy to announce that the qPCR-based mycoplasma detection service will be offered again on the first Wednesday of every month starting from October, just as before.

Key features of our detection protocol include (https://labsupport.pages.ist.ac.at/mycoplasma-detection/):

• Real-time PCR technology for rapid quantitative and qualitative analysis with high sensitivity
• Multiplex primers and probes targeting conserved mycoplasma DNA sequences
• Internal controls to ensure assay accuracy and sample quality
• Direct use of culture supernatant, no DNA extraction required

Please find below the sample preparation instructions (also available online here: https://labsupport.pages.ist.ac.at/mycoplasma-detection-guidelines/)

1. Cultivate cells without antibiotics for at least one week.
2. Collect 100 µL of supernatant from a culture at 90-100% confluence (grown for 2-3 days in the same media).
3. Heat-inactivate the supernatant at 95°C for 5 minutes. Note: Samples are stable at 4°C for up to 1 week.
4. Deliver samples to the 4°C fridge at the Sunstone Building, 1st Floor (I23.01.038). Tubes should be clearly labeled with user initials, sample number, and date (e.g., FS01_1oct25, FS02_1oct25). Printed labels are preferred.
5. Create a PPMS order, this triggers an automated notification to us.

Pricing details are available here (login required): https://labsupport.pages.ist.ac.at/mycoplasma-detection-pricing-internal-rates/  and below:

Dear cell culture users,

We are happy to announce that the qPCR-based mycoplasma detection service will be offered again on the first Wednesday of every month starting from October, just as before.

Key features of our detection protocol include (https://labsupport.pages.ist.ac.at/mycoplasma-detection/):

• Real-time PCR technology for rapid quantitative and qualitative analysis with high sensitivity
• Multiplex primers and probes targeting conserved mycoplasma DNA sequences
• Internal controls to ensure assay accuracy and sample quality
• Direct use of culture supernatant, no DNA extraction required

Please find below the sample preparation instructions (also available online here: https://labsupport.pages.ist.ac.at/mycoplasma-detection-guidelines/)

1. Cultivate cells without antibiotics for at least one week.
2. Collect 100 µL of supernatant from a culture at 90-100% confluence (grown for 2-3 days in the same media).
3. Heat-inactivate the supernatant at 95°C for 5 minutes. Note: Samples are stable at 4°C for up to 1 week.
4. Deliver samples to the 4°C fridge at the Sunstone Building, 1st Floor (I23.01.038). Tubes should be clearly labeled with user initials, sample number, and date (e.g., FS01_1oct25, FS02_1oct25). Printed labels are preferred.
5. Create a PPMS order, this triggers an automated notification to us.

Pricing details are available here (login required): https://labsupport.pages.ist.ac.at/mycoplasma-detection-pricing-internal-rates/  and below:

Dear cell culture users,

We are happy to announce that the qPCR-based mycoplasma detection service will be offered again on the first Wednesday of every month starting from October, just as before.

Key features of our detection protocol include (https://labsupport.pages.ist.ac.at/mycoplasma-detection/):

• Real-time PCR technology for rapid quantitative and qualitative analysis with high sensitivity
• Multiplex primers and probes targeting conserved mycoplasma DNA sequences
• Internal controls to ensure assay accuracy and sample quality
• Direct use of culture supernatant, no DNA extraction required

Please find below the sample preparation instructions (also available online here: https://labsupport.pages.ist.ac.at/mycoplasma-detection-guidelines/)

1. Cultivate cells without antibiotics for at least one week.
2. Collect 100 µL of supernatant from a culture at 90-100% confluence (grown for 2-3 days in the same media).
3. Heat-inactivate the supernatant at 95°C for 5 minutes. Note: Samples are stable at 4°C for up to 1 week.
4. Deliver samples to the 4°C fridge at the Sunstone Building, 1st Floor (I23.01.038). Tubes should be clearly labeled with user initials, sample number, and date (e.g., FS01_1oct25, FS02_1oct25). Printed labels are preferred.
5. Create a PPMS order, this triggers an automated notification to us.

Pricing details are available here (login required): https://labsupport.pages.ist.ac.at/mycoplasma-detection-pricing-internal-rates/  and below:

Dear cell culture users,

We are happy to announce that the qPCR-based mycoplasma detection service will be offered again on the first Wednesday of every month starting from October, just as before.

Key features of our detection protocol include (https://labsupport.pages.ist.ac.at/mycoplasma-detection/):

• Real-time PCR technology for rapid quantitative and qualitative analysis with high sensitivity
• Multiplex primers and probes targeting conserved mycoplasma DNA sequences
• Internal controls to ensure assay accuracy and sample quality
• Direct use of culture supernatant, no DNA extraction required

Please find below the sample preparation instructions (also available online here: https://labsupport.pages.ist.ac.at/mycoplasma-detection-guidelines/)

1. Cultivate cells without antibiotics for at least one week.
2. Collect 100 µL of supernatant from a culture at 90-100% confluence (grown for 2-3 days in the same media).
3. Heat-inactivate the supernatant at 95°C for 5 minutes. Note: Samples are stable at 4°C for up to 1 week.
4. Deliver samples to the 4°C fridge at the Sunstone Building, 1st Floor (I23.01.038). Tubes should be clearly labeled with user initials, sample number, and date (e.g., FS01_1oct25, FS02_1oct25). Printed labels are preferred.
5. Create a PPMS order, this triggers an automated notification to us.

Pricing details are available here (login required): https://labsupport.pages.ist.ac.at/mycoplasma-detection-pricing-internal-rates/  and below:

Dear cell culture users,

We are happy to announce that the qPCR-based mycoplasma detection service will be offered again on the first Wednesday of every month starting from October, just as before.

Key features of our detection protocol include (https://labsupport.pages.ist.ac.at/mycoplasma-detection/):

• Real-time PCR technology for rapid quantitative and qualitative analysis with high sensitivity
• Multiplex primers and probes targeting conserved mycoplasma DNA sequences
• Internal controls to ensure assay accuracy and sample quality
• Direct use of culture supernatant, no DNA extraction required

Please find below the sample preparation instructions (also available online here: https://labsupport.pages.ist.ac.at/mycoplasma-detection-guidelines/)

1. Cultivate cells without antibiotics for at least one week.
2. Collect 100 µL of supernatant from a culture at 90-100% confluence (grown for 2-3 days in the same media).
3. Heat-inactivate the supernatant at 95°C for 5 minutes. Note: Samples are stable at 4°C for up to 1 week.
4. Deliver samples to the 4°C fridge at the Sunstone Building, 1st Floor (I23.01.038). Tubes should be clearly labeled with user initials, sample number, and date (e.g., FS01_1oct25, FS02_1oct25). Printed labels are preferred.
5. Create a PPMS order, this triggers an automated notification to us.

Pricing details are available here (login required): https://labsupport.pages.ist.ac.at/mycoplasma-detection-pricing-internal-rates/  and below: