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Cd127 hil 7r m21

Manufactured by BD
Sourced in United States

The CD127 (HIL-7R-M21) is a laboratory equipment product. It is a cell surface marker that serves as a receptor for the cytokine interleukin-7 (IL-7). The CD127 molecule is expressed on a variety of immune cells, including T cells, B cells, and natural killer cells.

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4 protocols using cd127 hil 7r m21

1

Multiparametric Flow Cytometry for PBMC Analysis

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Distinct PBMC populations were enumerated by flow cytometry, as described (33 (link), 50 (link)). Phenotypic analyses were performed using Abs directed against CD3 (clone SP34-2), CD4 (L200), CD8 (RPA-T8), CD14 (M5E2), CD20 (2H2), CD45RA (5H9), CD56 (MY31) and CD127 (HIL-7R-M21) from BD Pharmingen (Franklin Lakes, NJ). Anti-CD159a (NKG2A) (Z199) was from Beckman Coulter and anti-CD28 (CD28.2) from Biolegend (San Diego, CA). Anti-CD25 (BC96) was from eBioscience (San Diego, CA) and anti-CD62L (SK11) from Becton Dickinson (Franklin Lakes, NJ). Data were acquired on a LSR II or LSR Fortessa (BD Bioscience) and analyzed with FlowJo software.
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2

Comprehensive T cell Immunophenotyping

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T cells were labeled with monoclonal antibodies against CD4 (OKT4), CD25 (BC96), CD38 (HIT1), CD48 (TU145), CD52 (4C8), CD127 (HIL-7R-M21), CD161 (HP-3G10), CD196 (11A9), and CD226 (DX11), all from BD or Biolegend, as described previously (12 (link)). Intracellular staining for HIF-1a (241812 from R&D systems) and AhR (T49-550 from BD) was done after fixation and permeabilization using kit from R&D Systems. The profiling was done after 7 days in culture if not mentioned otherwise in the figure legend. The data acquisition was done at LSRFortessa (BD biosciences), and analysis was performed with FlowJo v10 software (Tree star).
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3

Multi-Parameter Flow Cytometry Immunophenotyping

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The following anti-human mAb were used to stain cell suspension for FACS analysis: CD3 (SK7), CD4 (SK3), CD34 (581), CD8 (SK1), CD19 (HIB19), CD10 (HI10a), CD38 (HB7), NKp46 (9E2), CD16 (3G8), CD161 (DX12), CD56 (B159), HLA-DR (L243), CD244.2 (2B4), HLA-A/B/C (G46-2.6), CD117 (YB5.B8), CD14 (M5E2), CD122 (Mik-3), TCR-β (T10B9.1A-31), CD127 (hIL-7R-M21), CD11c (B-ly6), CD7 (M-T701), CD45 (2D1) from (BD Bioscience, CA, USA). All washings and reagent dilutions were done with phosphate buffered saline (PBS) containing 2% foetal calf serum (FCS). All acquisitions were performed using FACSVerse cytometers and cell sorting was perform using FACS ARIA, all machines were interfaced to the FACS-Diva software (BD Bioscience). Data analysis was performed using FlowJo software from TreeStar Inc. (Ashland, OR, USA).
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4

Isolation and Sorting of CD8+ T Cell Subsets

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PBMCs were isolated from fresh whole blood using Ficoll-Paque Plus (GE) density gradient centrifugation. For cell sorting, we used fluorochrome-labeled antibodies specific for CD3 (UCHT1), CD27 (M-T271) (Biolegend), CD4 (RPA-T4), CD19 (HIB19), IgD (IA6–2), CD127 (HIL-7R-M21) (BD Biosciences), and CD8 (SCF121Thy2D3) (Beckman-Coulter). CD8+IL7R+ (CD8+CD127+) and CD8+IL7R (CD8+CD127) T cells were sorted from the CD19CD3+CD4 fraction. Cell sorting was performed using FACSAria Fusion (BD).
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