permeabilization buffer perm/wash (Thermo Fisher)
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Permeabilization Buffer Perm/Wash, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/permeabilization+buffer+perm/permeabilization+buffer/pm40286451-176-10-13
Average 90 stars, based on 1 article reviews
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other:Article Title: Protocol for phenotyping and isolation of dendritic cell subsets from blood and lymphoid organs of non-human primates and humans by flow cytometry Article Snippet: Staining:Article Title: Succinate enhances mitochondrial metabolism and phagocytosis in human airspace monocytes Article Snippet: Cells were fixed (IC Fixation Buffer, Invitrogen) for 20 mins on ice. .. Cells were stained for intracellular markers ( ) overnight at 4°C in Article Title: Integrin CD103 reveals a distinct developmental pathway of autoreactive thymocytes in TCR transgenic mice Article Snippet: For cytokine production analysis, freshly isolated lymph node cells were resuspended in cell culture media at 5 \documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \usepackage{upgreek} \setlength{\oddsidemargin}{-69pt} \begin{document}$$\times$$\end{document} × 10 6 cells/ml density and stimulated with 50 ng/ml PMA (Sigma-Aldrich), 1 μM ionomycin (Sigma-Aldrich), and 3 μg/ml Brefeldin A (Invitrogen) for 3 hours. .. Cells were then washed once with FACS buffer followed by cell surface staining, fixation by IC Fixation Buffer (eBioscience), and Article Title: Bispecific targeting of 4-1BB and CCR8 boosts antitumor immunity via Ti-Treg depletion and CD8 + activation Article Snippet: Surface staining was performed for 30 min on ice after a 10 min incubation on ice with an anti-mouse CD16/CD32 antibody (clone 93, Invitrogen) to block Fcγ receptors by using panels of appropriately diluted fluorochrome-conjugated antibodies against the following mouse proteins in different combinations: CD45.2 (BD Biosciences, 104), CD3 (Invitrogen, 145-2C11), CD4 (BD Biosciences, RM4-5), CD8 (eBioscience, 53-6.7), 4-1BB (eBioscience, 1785), CCR8 (Biolegand, SA214G2), CD44 (Biolegand, IM7), CD62L (Biolegand, MEL-14), PD-1 (Biolegand, 29F.1A12), Tim3 (BD Biosciences, 5D12) and a Fixable Viability Stain (BD Biosciences). .. For intracellular staining, mouse cells were fixed and permeabilized ( Article Title: Therapeutic radiation drives leptomeningeal dissemination of medulloblastoma through an innate immune process. Article Snippet: In brief Radiation, the most effective treatment for medulloblastoma, induces an innate immune response and opens the bloodbrain barrier, allowing for the intravasation of tumor cells into the blood circulation.. These circulating tumor cells can seed the leptomeninges, forming metastasis, the major cause of mortality in patients, whereas inhibition of inflammation abrogates radiationinduced metastasis. Article Title: Simulating CD8 T cell exhaustion: A comprehensive approach Article Snippet: .. Then washed with FACS:Article Title: Integrin CD103 reveals a distinct developmental pathway of autoreactive thymocytes in TCR transgenic mice Article Snippet: For cytokine production analysis, freshly isolated lymph node cells were resuspended in cell culture media at 5 \documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \usepackage{upgreek} \setlength{\oddsidemargin}{-69pt} \begin{document}$$\times$$\end{document} × 10 6 cells/ml density and stimulated with 50 ng/ml PMA (Sigma-Aldrich), 1 μM ionomycin (Sigma-Aldrich), and 3 μg/ml Brefeldin A (Invitrogen) for 3 hours. .. Cells were then washed once with FACS buffer followed by cell surface staining, fixation by IC Fixation Buffer (eBioscience), and Incubation:Article Title: Bispecific targeting of 4-1BB and CCR8 boosts antitumor immunity via Ti-Treg depletion and CD8 + activation Article Snippet: Surface staining was performed for 30 min on ice after a 10 min incubation on ice with an anti-mouse CD16/CD32 antibody (clone 93, Invitrogen) to block Fcγ receptors by using panels of appropriately diluted fluorochrome-conjugated antibodies against the following mouse proteins in different combinations: CD45.2 (BD Biosciences, 104), CD3 (Invitrogen, 145-2C11), CD4 (BD Biosciences, RM4-5), CD8 (eBioscience, 53-6.7), 4-1BB (eBioscience, 1785), CCR8 (Biolegand, SA214G2), CD44 (Biolegand, IM7), CD62L (Biolegand, MEL-14), PD-1 (Biolegand, 29F.1A12), Tim3 (BD Biosciences, 5D12) and a Fixable Viability Stain (BD Biosciences). .. For intracellular staining, mouse cells were fixed and permeabilized ( Article Title: Salivary gland transcriptomic analysis and immunophenotyping in the IL-14α transgenic mouse model of Sjögren's disease Article Snippet: Following a 5 min wash in cytometry buffer, cells were fixed and permeabilized using the eBioscience FoxP3/transcription factor staining buffer set (ThermoFisher) per the manufacturer's protocol. .. Cells were then resuspended in Article Title: Simulating CD8 T cell exhaustion: A comprehensive approach Article Snippet: .. Then washed with |
