• LuminUltra Technologies Ltd.
  • LuminUltra Technologies Ltd.
  • LuminUltra Technologies Ltd.
  • LuminUltra Technologies Ltd.
  • LuminUltra Technologies Ltd.
  • LuminUltra Technologies Ltd.
  • LuminUltra Technologies Ltd.
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Performing Tests - Quench–Gone Organic Modified


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In addition to eliminating ATP from dead cells, QGO-M tests remove interferences from oils and other organics to obtain a true measure of biological activity.

  cATP Analyses using QGO-M consists of the following steps:

Mix your sample to ensure homogenity. Remove the plunger from a 20mL syringe and attach a filter. Pour the appropriate volume of sample into the barrel of the syringe.

TIP: Alternatively, the syringe tip can be immersed into the sample and drawn into the barrel before attaching the filter, rather than pouring the sample into the barrel after attaching the filter. Be sure the syringe tip is clean if this mechanism is used.



Slowly push the entire sample volume through the filter and into a waste receptacle. Push the plunger far enough to filter the sample and stop to ensure that the filter remains wet. Detach the filter and remove the plunger.

NOTE: If the full volume of sample could not be filtered, record the actual volume processed.
TIP: If increased sensitivity is desired, filter additional sample by repeating 2.2 and 2.3 using the same syringe and filter.



Filter Washing
Re-attach the filter to the 20mL syringe barrel and use the micropipettor to add 5mL of LumiClean to the syringe barrel. Pass the LumiClean through the filter to dryness and collect into the waste receptacle.


Filter Drying
Detach the filter from the 20mL syringe barrel, and attach the filter to a 60mL syringe. While holding the filter tip over a waste receptacle, push the plunger through the barrel to dry the filter. Repeat this process a second time, first detaching the filter from the barrel before removing the syringe plunger

TIP: The same 60mL syringe can be used to dry many filters. As a rule of thumb, replace the 60mL syringe for every 20 tests performed, so long as the syringe is stored in a clean, dust-free location in its wrapper when not in use.


Re-attach the filter to the 20mL syringe barrel. Use the micropipettor to add 1mL of UltraLyse 7 to the barrel. Pass the UltraLyse 7 through the filter to dryness and collect in an unused 17x100mm test tube. This is called the Extraction Tube.


NOTE: At this point, the contents of the Extraction Tube can be capped and stored refrigerated between 2-8oC for up to 1 week prior to 2.7 and 2.8.


Add 9mL of UltraLute into the Extraction Tube. Cap and invert three times to mix. This is now called the Diluted Extraction Tube.

NOTE: At this point, the contents of the Diluted Extraction Tube are stable at room temperature for up to 4 hours.


Using the micropipettor, transfer 100µL of the Diluted Extraction Tube contents to a new 12x55mm test tube (the Assay Tube), add 2 drops (100µL) of Luminase, swirl gently five times, and insert into the Luminometer. Record RLUcATP for use in the final calculations.

NOTE: If RLUcATP < 10 on a Kikkoman Lumitester C-100 or C-110, you are below the low–detection limit. Report cATP (pg ATP/mL) = 0 in the final calculations, or select a larger volume in 2.1 and repeat the analysis.
TIP: If “Scale Over” is returned, repeat the analysis using a smaller sample volume in 2.1.




UltraCheck1 Standard

For each set of tests, an UltraCheck1 Standard must also be performed. This is used as a calibration to convert RLU values obtained from ATP assays into actual ATP concentrations:


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