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Molecular Diagnostics & Proteomics |
BD Vacutainer® CPT™ Cell Preparation Tube with Sodium Heparin
Procedure
- The BD Vacutainer® CPT™ Tube with Sodium Heparin should
be at room temperature (18-25° C) and properly labeled for
patient identification.
- Collect blood into the Tube using the standard technique for
BD Vacutainer® Brand Evacuated Blood Collection Tubes (see
Venipuncture Technique & Sample Collection section and Prevention
of Backflow section).
- After collection, store Tube upright at room temperature until centrifugation. Blood samples should be centrifuged within two hours of blood collection for best results.
- Centrifuge Tube/blood sample at room temperature (18-25° C) in a horizontal rotor (swing-out head) for a minimum of 15 minutes at 1500 to 1800 RCF (Rela-tive Centrifugal Force).
NOTE: Remix the blood sample immediately prior to centrifugation by gently inverting the Tube 8 to 10 times. Also, check to see that the Tube is in the proper centrifuge carrier/adapter.
WARNING: Excessive centrifuge speed (over 2000 RCF) may cause tube breakage and exposure to blood and possible injury. To calculate the correct centrifuge speed for a given RCF, use the following calculator. Simply enter two of the three values in the calculator and press the Calculate button.

- After centrifugation, mononuclear cells and platelets will be in a whitish layer just under the plasma layer (see above figure). Aspirate approximately half of the plasma without disturbing the cell layer. Collect cell layer with a Pasteur pipette and transfer to a 15 mL size conical centrifuge Tube with cap. Collection of cells immediately following centrifugation will yield best results.
- An alternative procedure for recovering the separated mononuclear
cells is to resuspend the cells into the plasma by inverting the
unopened BD Vacutainer® CPT™ Tube gently 5 to 10 times.
This is the preferred method for storing or transporting the separated
sample for up to 24 hours after centrifugation. To collect the
cells, open the BD Vacutainer® CPT™ Tube and pipette
the entire contents of the Tube above the gel into a separate
vessel.
Suggested Cell Washing Steps:
- Add PBS to bring volume to 15 mL. Cap Tube. Mix cells by inverting Tube 5 times.
- Centrifuge for 15 minutes at 300 RCF. Aspirate as much supernatant as possible without disturbing cell pellet.
- Resuspend cell pellet by gently vortexing or tapping Tube with index finger.
- Add PBS to bring volume to 10 mL. Cap Tube. Mix cells by inverting Tube 5 times.
- Centrifuge for 10 minutes at 300 RCF. Aspirate as much supernatant as possible without disturbing cell pellet. Resuspend cell pellet in the desired medium for subsequent procedure.
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