MBTP 29: Immunophenotyping of antigen-specific CD4+ T cells from human PBMCs using flow cytometry
Miltenyi Biotec-tested panel 29 (MBTP 29)
Miltenyi Biotec-tested panel 29 (MBTP 29)
This application protocol describes the flow cytometric analysis of antigen-specific CD4+ T cells from human PBMCs.
Protocol
Labeling of cells with Viobility™ Fixable Dye
- Viobility Fixable Dye was reconstituted in advance. The vial was warmed up to room temperature to avoid water condensation. One vial of lyophilized Viobility Fixable Dye was reconstituted by addition of 100 µL anhydrous DMSO to the dye vial and mixed until completely dissolved. The solution was aliquoted and stored at –20 °C under anhydrous (desiccant) conditions and protected from light for up to one month.
- Volumes given below were for up to 107 nucleated cells. When working with fewer than 107 cells, use the same volumes as indicated. When working with higher cell numbers, scale up all reagent volumes and total volumes accordingly (e.g. for 2×107 nucleated cells, use twice the volume of all indicated reagent volumes and total volumes).
- Cell number was determined.
- Cells were washed by addition of 1 mL of 1× PBS and centrifuged at 300×g for 10 minutes. Supernatant was aspirated completely.
- Cells were resuspended in 100 µL of 1× PBS.
- 1 µL of Viobility Fixable Dye was added.
- Samples were mixed well and incubated for 15 minutes in the dark at room temperature.
▲Note: Higher temperatures and/or longer incubation times may lead to non-specific cell labeling. Working on ice requires increased incubation times. - Cells were washed by addition 1 mL PEB buffer and centrifuged at 300×g for 10 minutes. Supernatant was aspirated completely.
- Step 6 was repeated.
- Surface staining was performed.
Surface staining
- Volumes given below were for up to 106 nucleated cells. When working with fewer than 106 cells, use the same volumes as indicated. When working with higher cell numbers, scale up all reagent volumes and total volumes accordingly (e.g. for 2×106 nucleated cells, use twice the volume of all indicated reagent volumes and total volumes).
- Cell number was determined.
- Cells were centrifuged at 300×g for 10 minutes. Supernatant was aspirated completely.
- A master mix with all antibodies was prepared according to the dilutions mentioned in the respective antibody data sheets.
- 100 µl antibody master mix was added to the cells.
- Cells were resuspended and incubated for 10 minutes in the dark at 4 °C.
- Cells were washed by addition of 1 mL of PEB buffer and centrifuged at 300×g for 5 minutes at 4 °C. Supernatant was aspirated completely.
- Cells were resuspended in 100 µL of PEB buffer and flow cytometric analysis was performed using the MACSQuant® Analyzer.
Materials
Antibody panel details
| Specificity | Clone | Purpose | Fluorochrome | Detection filter (nm) (laser) |
| Viobility™ 405/520 Fixable Dye | - | Viability | - | 525/50 (violet) |
| CD3 | BW264/56* | T cells | VioBlue® | 450/50 (violet) |
| CD4 | M-T466* | T helper cells | PerCP-Vio® 770 | 655–730 (blue) |
| CD154 | REA238 | Activation marker | PE | 585/40 (blue) |
| CD185 (CXCR5) | REA103 | Antigen-specific cells | PE-Vio 770 | 750 LP (blue) |
| CD183 (CXCR3) | REA232 | Follicular T helper cells 1 | Vio Bright FITC | 525/50 (blue) |
| CD196 (CCR6) | REA190 | Follicular T helper cells 17 | APC | 655-730 (red) |
*alternative REAfinity™ Antibody available
Additional reagents used
- Phosphate-buffered saline (PBS), pH 7.2
- PEB buffer: PBS, pH 7.2, 0.5% bovine serum albumin (BSA), and 2 mM EDTA.
- Deionized or distilled water
- Flow cytometer, for example, MACSQuant® Analyzer 10 (# 130-096-343) or MACSQuant X (# 130-105-100)
- (Optional) MACSQuant Calibration Beads (# 130-093-607)
- (Optional) MACS® Comp Bead Kit, anti-REA (# 130-104-693)
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REA103
FC
USD 365.00
REA232
FC
USD 405.00
