Phosphatidylcholine Assay Kit

1. 96-well Microtiter Plate : One 96-well clear bottom black plate.
2. Assay Buffer (10X) : One 25 mL bottle.
3. Fluorescence Probe (100X) : One 100 μL tube in DMSO.
4. HRP : One 100 μL tube of 100 U/mL HRP solution in glycerol.
5. Standard Diluent (10X) : One 1 mL tube.

Box 2 (shipped on blue ice packs)

1. Distilled or deionized water
2. 1X PBS
3. 10 μL to 1000 μL adjustable single channel micropipettes with disposable tips
4. 50 μL to 300 μL adjustable multichannel micropipette with disposable tips
5. Multichannel micropipette reservoir
6. Fluorescence microplate reader capable of reading excitation in the 530-570 nm range and emission in the 590-600 nm range.
7. (optional) Chloroform
8. (optional) Superoxide dismutase

• Simple fluorometric assay
• Measures phosphatidylcholine levels in plasma or serum, tissue homogenates, or cell suspensions
• Detect as little as 0.5 mg/dL

• 1X Assay Buffer: Warm the Assay Buffer (10X) to room temperature prior to using. Dilute the Assay Buffer (10X) with deionized water by diluting the 25 mL Buffer with 225 mL deionized water for 250 mL total. Mix to homogeneity. Store the 1X Assay Buffer at 4 °C up to six months.
• 1X Standard Diluent: Warm the Standard Diluent (10X) to room temperature prior to using. Dilute the Standard Diluent (10X) with deionized water by diluting the 1 mL Diluent with 9 mL deionized 4 water for 10 mL total. Vortex to homogeneity. Store the 1X Standard Diluent at 4 °C up to six months.
• Reaction Reagent: Prepare a Reaction Reagent by diluting the Choline Oxidase 1:200, HRP 1:500, Fluorescence Probe 1:100, and Phospholipase D 1:350 in 1X Assay Buffer. (e.g. for 50 assays, combine 25 μL of Choline Oxidase, 10 μL of HRP, 50 μL Fluorescence Probe, and 15 μL Phospholipase D with 1X Assay Buffer to 5 mL total solution). Mix thoroughly and protect the solution from light. For best results, place the Reaction Reagent on ice and use within 30 minutes of preparation. Do not store the Reaction Reagent solution. Note: The Fluorescence Probe is light sensitive and must be stored accordingly.

Samples should be assayed immediately or stored at -80 °C prior to performing the assay. Optimal experimental conditions for samples must be determined by the investigator. The following recommendations are only guidelines and may be altered to optimize or complement the user's experimental design. A set of serial dilutions is recommended for samples to achieve optimal assay results and minimize possible interfering compounds. Run proper controls as necessary. Always run a standard curve with samples. • Tissues or Cell Suspensions: Homogenize 250 mg of sample (wet tissue or cell pellet) in 4.5 mL of chloroform/methanol (2:1, v/v). Centrifuge to remove debris. After centrifugation, incubate the homogenate at room temperature for 1 hour on an orbital shaker. Induce phase separation by adding 1.25 mL dH2O. Incubate 10 minutes at room temperature and centrifuge at 1000 x g for 10 minutes. Collect the lower (chloroform) organic phase and re-extract the upper phase with 2 mL of solvent mixture whose composition is CHCl3/MeOH/water (86:14:1, v/v/v). Combine organic phases and dry in a vacuum centrifuge. Dissolve in 200 μL CHCl3/MeOH/water (60:30:4.5, v/v/v) for storage. Before phosphatidylcholine assay, samples must be diluted at least 1:50 to 1:400 with Assay Buffer. • Serum: Collect blood without using an anticoagulant. Allow blood to clot for 30 minutes at room temperature. Centrifuge at 2000 x g and 4 °C for 10 minutes. Remove the serum layer and store on ice. Take care to avoid disturbing the white buffy layer. Aliquot samples for testing and store remaining solution at -80 °C. Perform serum dilutions in 1X Assay Buffer. Serum samples must be diluted at least 1:50 to 1:400 with Assay Buffer. This will provide values within the range of the standard curve. • Plasma: Collect blood with heparin or citrate and centrifuge at 1000 x g and 4 °C for 10 minutes. Remove the plasma layer and store on ice. Take care to avoid disturbing the white buffy layer. Aliquot samples for testing and store remaining solution at -80 °C. Perform plasma dilutions in 1X Assay Buffer. Plasma samples must be diluted at least 1:50 to 1:400 with Assay Buffer. This will provide values within the range of the standard curve. Notes:

1. Samples with NADH concentrations above 10 μM and glutathione concentrations above 50 μM will oxidize the probe and could result in erroneous readings. To minimize this interference, it is recommended that superoxide dismutase (SOD) be added to the reaction at a final concentration of 40 U/mL. 5
2. Avoid samples containing DTT or β-mercaptoethanol since the fluorescence probe is not stable in the presence of thiols (above 10 μM).
3. Choline can generate high background if present in samples. If choline may be present, run a background control without Phospholipase D. Subtract this value from sample reading values.

Each phosphatidylcholine standard and sample should be assayed in duplicate or triplicate. A freshly prepared standard curve should be used each time the assay is performed.

1. Add 10 μL of the diluted phosphatidylcholine standards or samples to the 96-well microtiter plate.
2. Add 100 μL of the prepared Reaction Reagent to each well and mix the well contents thoroughly.
3. Cover the plate wells to protect the reaction from light. Incubate the plate for 60 minutes at 37 °C.
4. Read the plate with a fluorescence microplate reader equipped for excitation in the 530-570 nm range and for emission in the 590-600 nm range.
5. Calculate the concentration of phosphatidylcholine within samples by comparing the sample RFU to the phosphatidylcholine standard curve. 6

1. Calculate the average fluorescence values for every standard, control, and sample. Subtract the average zero standard value from itself and all standard and sample values. This is the corrected fluorescence.
2. Plot the corrected fluorescence for the standards against the final concentration of the phosphatidylcholine standards from Table 1 to determine the best curve. See Figure 2 for an example standard curve.
3. Determine the phosphatidylcholine concentration of the samples with the equation obtained from the linear regression analysis of the standard curve. Substitute the corrected fluorescence values for each sample. Remember to account for dilution factors. Sample corrected fluorescence Total Phosphatidylcholine (mg/dL) = x Sample dilution Slope 7 RFU