Isolate untouched mouse CD4+ T cells by depleting non-CD4+ T cells (CD8+ T cells, B cells, monocytes/ macrophages NK cells, dendritic cells, erythrocytes and granulocytes) from mouse spleen or lymph node cells. Other sources of mouse CD4+ T cells can also be used as starting material after optimization for the particular application. Isolated CD4+ T cells are bead- and antibody-free and are suitable for any downstream application
Principle of Isolation
Add a mixture of monoclonal antibodies against the non-CD4+ T cells to the starting sample. Add Mouse Depletion Dynabeads to bind to the non-CD4+ T cells during a short incubation. Separate the bead-bound cells by a magnet. Discard the beadbound cells and use the remaining, untouched mouse CD4+ T cells for any application
Description of Materials
Dynabeads are uniform, superparamagnetic polystyrene beads (4.5 μm diameter) coated with a polyclonal sheep anti-rat IgG antibody.
Dynal® Mouse CD4 Negative Isolation Kit
|Number of cells Processed||Up to 1 × 109||Up to 2 × 108|
|Mouse Depletion Dynabeads||2 × 10 ml||4 ml|
|Antibody Mix||2 ml||0.4 ml|
* Starter Kit
- Mouse Depletion Dynabeads - Supplied at 4 × 108 beads per ml in phosphate buffered saline (PBS), pH 7.4, containing 0.1% bovine serum albumin (BSA) and 0.02% sodium azide (NaN3).
- Antibody Mix - The Antibody Mix contains a mixture of rat monoclonal antibodies against mouse CD45R (B220), CD11b (MAC-1), Ter-119, CD16/32 and CD8. Supplied in PBS with 0.02% sodium azide (NaN3).
Additional Materials Required
- Heat inactivated Fetal Calf Serum (FCS).
- Mixer allowing both tilting and rotation.
- Buffer 1: PBS (without Ca2+ and Mg2+) w/0.1% BSA and 2 mM EDTA, pH 7.4.
- BSA can be replaced by FCS.
- EDTA can be replaced by sodium citrate.
- PBS containing Ca2+ or Mg2+ is not recommended.
- This product should not be used with the magnet MPC-1.
- Keep the buffers cold!
Dynabeads Washing Procedure
Dynabeads should be washed before use.
1. Resuspend the Dynabeads in the vial.
2. Transfer the desired volume of Dynabeads to a tube.
3. Add the same volume of Buffer 1, or at least 1 ml, and mix.
4. Place the tube in a magnet for 1 min and discard the supernatant.
5. Remove the tube from the magnet and resuspend the washed Dynabeads in the same volume of Buffer 1 as the initial volume of Dynabeads.
See recommended procedure to prepare cells from mouse spleen or lymph nodes.
Critical Steps for Cell Isolation
- Use a mixer that provides tilting and rotation of the tubes to ensure Dynabeads do not settle at the bottom of the tube.
- Never use less than 200 μl Dynabeads per 1 x 107 leucocytes
- It is critical to follow the magnet recommendations to ensure a successful isolation.
Isolation of Mouse CD4+ T Cells from Spleen or Lymph Node Leucocytes
This protocol is based on 1 x 107 leucocytes. It is scalable from 1 x 107-1 x 109 cells, (see table 1).
- Transfer 100 μl (1 x 107) leucocytes in Buffer 1 to a tube.
- Add 20 μl heat inactivated FCS.
- Add 20 μl of Antibody Mix.
- Mix well and incubate for 20 min at 2-8°C.
- Wash the cells by adding 2 ml Buffer 1. Mix well by tilting the tube several times and centrifuge at 300 x g for 8 min at 2-8°C. Discard the supernatant.
- Resuspend the cells in 800 μl Buffer 1.
- Add 200 μl pre-washed Mouse Depletion Dynabeads.
- Incubate for 15 min at 18-25°C with gentle tilting and rotation.
- Resuspend the bead-bound cells by gently pipetting 5 times using a pipette with a narrow tip opening, (e.g. a 1000 μl pipette tip or a 5 ml serological pipette).
- Add 1 ml Buffer 1.
- Place the tube in the magnet for 2 min.
- Transfer the supernatant to a new tube.
The supernatant contains the negatively isolated mouse CD4+ T cells.
Table 1. Volumes for mouse T cell isolation per 1 x 107 starting leucocytes.
|Working volume per 1 x 107 leucocytes|
|Cell volume (step 1)||100 μl|
|FCS (step 2)||20 μl|
|Antibody Mix (step 3)||20 μl|
|Washing (step 5)||2 ml|
|Resuspension (step 6)||800 μl|
|Mouse Depletion Dynabeads (step 7)||200 μl|
|Volume added before magnet (step 10)||1 ml|
When working with higher cell numbers, scale up all reagents and volumes accordingly (e.g. for 2 x 107 leucocytes use twice the volume of all indicated reagent volumes). As a rule of thumb, up to 5 x 107 leucocytes can be processed in a single 15 ml tube and up to 2 x 108 leucocytes can be processed in a single 50 ml tube.
Isolated mouse CD4+ T cells can be used in applications such as cell culture, flow cytometry, functional assays and molecular studies.
Description of Materials
Dynabeads FlowComp™ are uniform, superparamagnetic beads (2.8 μm in diameter). Supplied at a concentration of approx. 1 × 10 9 beads (10 mg) per ml in phosphate buffered saline (PBS), pH 7.4, containing 0.1% bovine serum albumin (BSA) and 0.02% sodium azide (NaN 3) as pereservatives.
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 .
- Comer JE et al (2005). Direct Inhibition of T-Lymphocyte Activation by Anthrax Toxins In Vivo. Infection and Immunity, vol 73 (12), pp. 8275-8281.
- Toscano MA et al (2007). Differential glycosylation of TH1, TH2 and TH-17 effector cells selectively regulates susceptibility to cell death. Nature Immunology, vol 8 (8), pp.825-834.