ELISA for human CXCL12/SDF-1α
						R&D Systems ELISA for human CXCL12/SDF-1α
Judith Sunzenauer (last update 11.6.2013)
Procedures
Preparation:
- Bring all reagents and samples to room temperature before use.
 - Run duplicates.
 - Samples: an additional centrifugation step at 10.000xg for 10min at 4°C is necessary. Dilute EDTA plasma samples 1:4 with Calibrator Diluent RD6Q.
 - Prepare Wash Buffer: Add 20ml of Wash Buffer Concentrate to 480ml a.dest (1:25 Dilution)
 - Reconstitute CXCL12 Standard: add 1ml a.dest to vial of CXCL12 Standard (concentration of stock: 100.000pg/ml). Allow the standard to sit for a minimum of 30min prior to making dilutions.
 
- Produce the dilution series for CXCL12 Standardcurve:
 
Prepare 8 prelabeled polypropylene tubes and fill each tube with 500µl of Calibrator Diluent RD6Q excluding #1 which is filled with 900µl. Transfer 100µl Standard from the original vial to tube #1, mix thoroughly and transfer 500µl from tube #1 to #2,….. continue until tube #7. Fill tube #8 with Calibrator Diluent RD6Q.
Assay Procedure:
- Add 100µl of Assay Diluent RD1-55 to each well.
 - Add 100µl of Standard Dilution #1-8 or sample per well.
 - Seal the Plate and incubate 2h at room temperature on a horizontal orbital microplate shaker set at 500rpm.
 
- Aspirate each well.
 - Wash 4 times with 400µl Wash Buffer.
 - After the last wash, remove any remaining liquid and invert the plate and blot it against clean paper towels.
 - Add 200µl of CXCL12/SDF1a Conjugate to each well.
 - Seal and incubate for 2h at RT on the shaker.
 
Prepare Substrate Solution: mix color Reagents A and B in equal volumes within 15min of use. Protect from light!
- Wash 4 times with 400µl Wash Buffer.
 - Add 200µl of Substrate Solution to each well.
 - Incubate for 30min at RT and protect from light.
 
- Add 50µl Stop Solution to each well. Gently tap the plate to ensure mixing.
 - Determine the OD at 450nm within 30min. Set wavelength correction to 540nm or 570nm.
 
Calculation of Results:
- If samples have been diluted, the concentration read from the standard curve must be multiplied by the dilution factor.
 - Concentrations of the Standard Dilutions:
 
| Std. # | CXCL12 pg/ml | 
| 1 | 10.000 | 
| 2 | 5000 | 
| 3 | 2500 | 
| 4 | 1250 | 
| 5 | 625 | 
| 6 | 312 | 
| 7 | 156 | 
| 8 | 0 | 
Sensitivity:
| Assay | Mean in EDTA Plasma(pg/ml) | Range (pg/ml) | 
| CXCL12 | 2000 | 18-10.000 | 
Handling Photometer + Software:
Make sure the laser is warmed up prior to scanning for 15min
Materials
| 
 CXCL12 Human Immunoassay  | 
 R&D Systems  | 
 #SSA00  |