Editing Mycoplasma Assay Protocol (section)

=Protocol=

====Preparing the Assay====

# Head over to the Nathanson Lab main room. It is located at '''CHS 23-234'''. You should contact someone ahead of time. Otherwise, any '''Lucetta 2 Luminometer''' will do.
# Next, '''take out a microtiter plate''' designated for biohazardous samples. The ''Nathanson Lab'' usually keeps a few in use in the middle drawer on the first lab bench once you enter the room. These microtiter plates are often used for assays involving mouse blood, so treat them as biohazardous. You should do the same if you use your own plate.
# In the microtiter plate, '''place 100 µL of sample (or control) into unused wells'''.
# Place the plate in your biohazardous secondary container for transport.
# Go to the assay room at '''CHS 23-376'''. A member of the ''Nathanson Lab'' will likely need to accompany you to let you in and log you into the machine.
# To each sample, '''add 100 µL of thawed MycoAlert Reagent''' (labeled “R” on aliquots) and '''wait 5 minutes'''.

====Running the Assay====

# Boot up the '''CLARIOstar program'''.
# Select '''Manage Protocols''' and then click on '''Myco Test'''.
# In the window, click on the '''Layout tab''' and '''Empty''' out all cell wells. You can do this by selecting the entire plate and clicking on the '''Empty''' button.
# Click '''Sample''' and select the wells on the plate that contain your samples (including the control). Click '''Start Measurement'''.
# In the second window that pops up, uncheck '''Gain Adjustment'''.
# Once '''your 5 minutes are up''', push the small black button above the myco tray insert on the machine to open it. '''Place your microtiter plate into the tray'''.
# On the new window in ''CLARIOstar'', double check that '''Gain Adjustment''' is unchecked. Then, hit '''Start Measurement''' when you’re ready.
# Once the program is finished, '''write down the values that pop up for each sample'''. These values are your '''first measurement (A)'''.
# Remove the microtiter plate from the machine.
# Next, '''add 100 µL of thawed MycoAlert Substrate''' (labeled “S” on aliquots) to each sample. '''Wait 10 minutes'''.
# Repeat steps 2-5. Ensure that '''Gain Adjustment''' is unchecked, and then run again.
# Once the program is finished, '''write down the values that pop up for each sample'''. These values are your '''second measurement (B)'''.
# Close the application and log off the computer (if in the ''Nathanson Lab'', leave it on). Return the microtiter plate to where you found it, if in the ''Nathanson Lab'' (no need to aspirate the samples), otherwise dispose of the media as if it were biohazardous. Sterilize your biohazardous secondary container with 70% isopropyl alcohol.

Next, calculate the following ratio for each of your samples, where '''B''' is your reading after adding MycoAlert Substrate and '''A''' is your reading after adding MycoAlert Reagent. Use the table below to determine the outcome of the assay. 

{| class="wikitable"
|+MycoAlert Result: Ratio = B/A
|-
! scope="col"| Ratio Value
! scope="col"| Result from the MycoAlert Assay
|-
|Less than 1.0
| Negative for mycoplasma.
|-
|1.0-1.2
|Inconclusive. Quarantine the cells for 24-48 hours and retest.
|-
|Greater than 1.2
|Positive for mycoplasma.
|}