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Pharmingen foxp3 staining kit

Manufactured by BD
Sourced in China

The BD Pharmingen FoxP3 staining kit is a laboratory reagent used for the detection and analysis of FoxP3-expressing cells, a key transcription factor associated with regulatory T cells. The kit provides the necessary reagents and protocols to perform intracellular staining of FoxP3 in fixed and permeabilized cells.

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2 protocols using pharmingen foxp3 staining kit

1

Ins2 Peptide-Loaded Hydrogel Vaccine for NOD Mice

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2‐Cl‐trityl chloride resin (1.1 mmol g−1) was obtained from Nankai University resin Co., Ltd. Fmoc‐amino acids and o‐benzotriazol‐1‐yl‐N,N,N′,N′‐tetramethyluronium hexafluorophosphate (HBTU) were acquired from GL Biochem (Shanghai). Hydogels were prepared and respective endotoxin levels of formula were tested as previously reported.[23, 24] Ins29‐23 peptide (SHLVEALYLVCGERGR; endotoxins <1 EU mg−1) was supplied by Bankpeptide (Hefei, China). The BD Pharmingen FoxP3 staining kit was from (BD Biosciences, Beijing, China). Aluminum hydroxide was purchased from Sigma‐Aldrich (Shanghai, China). Antibodies used for flow cytometry analysis were purchased from eBioscience (CA, USA) and antibodies used for immunofluorescence staining were obtained from Abcam (Shanghai, China). Cytokine chip microarray was performed by Beijing Genomics Institute (Beijing, China). Recombinant Human Insulin R/CD220 (aa 28‐944) Protein was ordered from R&D Systems (Shanghai, China). Mouse Insulin EZRMI‐13 ELISA kit was from Millipore (Merck, UK). Female NOD/ShiLtJNju mice were supplied by Model Animal Research Center of Nanjing University. All animal procedures were approved by the Centre of Tianjin Animal Experiment Ethics Committee. The accreditation number of the laboratory is SYXK(Jin) 2019‐0003 promulgated by Tianjin Science and Technology Commission.
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2

Quantification of Coronary T-Cell and Cytokine Profiles

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For quantification of the local T cell subset and immune‐inflammatory mediators, 20 mL of blood was collected from the coronary artery using an aspiration thrombectomy catheter immediately after the diagnostic angiogram but before the intervention.13, 14 For patients with multivessel coronary artery disease, the coronary blood sampling of each culprit vessel was collected separately for flow cytometry detection. T cell subsets and cytokine levels were detected using flow cytometry. Briefly, to quantify mature T, B, and NK lymphocyte populations and CD4+ and CD8+ T cell subsets in whole blood, BD MultitestTM four‐color reagents were used for flow cytometry (BD FACSCalibur). The activated T cells were tested using BD MultitestTM reagents, including monoclonal antibodies (CD3/CD4/CD8/CD38/CD25/HLA‐DR), and flow cytometry (BD FACSCanto). The percentage of Treg cells was detected using a BD Pharmingen™ FoxP3 Staining Kit and flow cytometry (BD FACSCanto). The quantification of cytokines was performed using BDTM Cytometric Bead Array (CBA) kits and flow cytometry (BD FACSCanto II).
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