Glucose Assay in Serum: Difference between revisions
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== Calculations == | == Calculations == | ||
* Use the standard curve to calculate glucose levels. | * Use the standard curve to calculate glucose levels. | ||
== Reading Plate Instructions == | |||
* Turn on the plate reader (switch at the back) and the computer. | |||
* Open ‘Soft Max Pro’. | |||
* Click ‘Settings’. | |||
* Set ‘Wavelengths’ to “2”. | |||
* Set ‘Lm1’ to “490”, ‘Lm2’ to “650”. | |||
* Put plate in, REMOVE THE LID. | |||
* Click ‘Read’. | |||
* Reading: top numbers are 490 uL, bottle numbers are 650 uL | |||
* To export files: click ‘file’ - ‘export’ - ‘save to computer’ - ‘Bridges’ folder - place in USB | |||
Revision as of 00:54, 13 February 2026
Materials
- FujiFilm Autokit Glucose (Cat 997-03001). Dissolve the Color Reagent in Buffer Solution (150 mL) to make a bottle of 150 mL Color Solution. The solution is stable for 2 weeks at 4C.
- Glucose Standard Solution (200 mg/dL)
- Serum samples (thaw on ice if from -80C)
Procedure
- Plan out 96-well plate, including samples and space for 5 standards and a blank, in duplicates.
- Add 100 uL of Color Solution to each well.
- Add 0, 1, 2, 3, 4, 5 uL to each of the standard wells.
- Add 3 uL of sample to each well.
- Incubate at room temperature for 30 mins (or 5 mins at 37C).
- Read plate at 505 nM and 600 nM.
Calculations
- Use the standard curve to calculate glucose levels.
Reading Plate Instructions
- Turn on the plate reader (switch at the back) and the computer.
- Open ‘Soft Max Pro’.
- Click ‘Settings’.
- Set ‘Wavelengths’ to “2”.
- Set ‘Lm1’ to “490”, ‘Lm2’ to “650”.
- Put plate in, REMOVE THE LID.
- Click ‘Read’.
- Reading: top numbers are 490 uL, bottle numbers are 650 uL
- To export files: click ‘file’ - ‘export’ - ‘save to computer’ - ‘Bridges’ folder - place in USB