Related Product Information
Principle of Isolation
Dynabeads are mixed with the sample in a tube. The Dynabeads will bind to the target cells during a short incubation, and then the bead-bound cells are separated by a magnet.
- Positive isolation – discard the supernatant and use the bead-bound cells for downstream molecular applications (e.g. protein or gene expression analysis).
- Depletion – discard the bead-bound cells and use the remaining, untouched cells for any application.
Isolate T cells directly from whole blood, buffy coat or MNC. Please visit www.invitrogen.com/cellisolation and follow our QuickLinks for recommended sample preparation procedures.
Additional Materials Required
Materials that are not included, but are needed to perform the entire protocol:
• Mixer allowing both tilting and rotation
• Magnet: See www.invitrogen.com/magnets-selection for magnet recommendations
• Isolation buffer: Ca2+ and Mg2+ free phosphate buffered saline (PBS) (e.g. Gibco cat.no. 14190-094) supplemented with 0.1% BSA and 2mM EDTA
BSA can be replaced by human serum albumin (HSA) or 2% FBS/FCS. EDTA can be replaced by 0.6% sodium citrate.
- Use a mixer that provides tilting and rotation of the tubes to ensure that Dynabeads do not settle at the bottom of the tube.
- Follow the recommended volumes and incubation times.
- Avoid air bubbles during pipetting.
Table 1: Volume of Dynabeads added per ml of sample.
|Sample volume ||1 ml||1 ml|
|Volume of Dynabeads||50 μl||100 μl|
|Total no. of cells processed per product||1x109||5x108|
* When working with lower cell concentrations, use the same volumes as indicated. When working with higher cell concentrations, scale up all reagent volumes and total volumes accordingly.
Dynabeads Washing Procedure
Dynabeads should be washed before use.
- Resuspend the Dynabeads in the vial.
- Transfer the desired volume of Dynabeads to a tube.
- Add the same volume of Isolation buffer, or at least 1 ml, and mix.
- Place the tube in a magnet for 1 min and discard the supernatant.
- Remove the tube from the magnet and resuspend the washed Dynabeads in the same volume of Isolation buffer as the initial volume of Dynabeads (bullet point 2).
Depletion or Positive Isolation of CD2+ cells
- Add the appropriate volume of Dynabeads to the prepared sample according to table 1.
- Incubate for 20 min (positive isolation) or 30 min (depletion) at 2 - 8°C with gentle tilting and rotation.
- Place the tube in a magnet for 2 min.
- For depletion, transfer supernatant to a new tube for further use.
- For positive isolation, discard the supernatant and wash the beadbound cells 3 times by resuspending in Isolation Buffer to the original sample volume, and separate using a magnet.
For molecular studies, lyse cells while still attached to the beads and transfer supernatant (lysate) to a new tube for further processing.
This product is stable until the expiry date stated on the label when stored unopened at 2-8°C. Store opened vials at 2-8°C and avoid bacterial contamination. Keep Dynabeads in liquid suspension during storage and all handling steps, as drying will result in reduced performance. Resuspend well before use.
Warnings And Limitations
This product is for research use only. Not intended for any animal or human therapeutic or diagnostic use unless otherwise stated. Follow appropriate laboratory guidelines. This product contains 0.02% sodium azide as a preservative, which is cytotoxic.
Avoid pipetting by mouth!
Sodium azide may react with lead and copper plumbing to form highly explosive metal azides. When disposing through plumbing drains, flush with large volumes of water to prevent azide build up. Certificate of Analysis (CoA) is available upon request. Material Safety Data Sheet (MSDS) is available at http://www.invitrogen.com.
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