anti cd206 pe Search Results


95
Miltenyi Biotec anti cd206 pe
Anti Cd206 Pe, supplied by Miltenyi Biotec, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Guangzhou JET Bio-Filtration pe anti-mouse cd206/mmr antibody
Pe Anti Mouse Cd206/Mmr Antibody, supplied by Guangzhou JET Bio-Filtration, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Miltenyi Biotec pe vio770 cd206 mabs
Flow cytometric analysis of the M1 markers HLA-DR and CD16 and the M2 markers <t>CD206</t> and CD163 on ( a ) M0, ( b ) polarized M(IFN-γ/LPS), and ( c ) polarized M(IL-10) macrophages. Macrophages (7 × 10 5 cells per mL) were stimulated or not with 10 −8 M NPY in the presence or absence of LPS in complete medium for 24 h and then analyzed for surface marker expressions by flow cytometry. Histograms show the percentages of positive cells (%) and the mean fluorescence intensity (MFI). Results are expressed as mean value ± SD of 4 independent experiments. Significance was determined by one-way ANOVA followed by Tukey’s post hoc analysis; *: p < 0.05, **: p < 0.01.
Pe Vio770 Cd206 Mabs, supplied by Miltenyi Biotec, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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pe vio770 cd206 mabs - by Bioz Stars, 2026-03
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90
AAT Bioquest pe-conjugated anti-human cd206/cd163
Flow cytometric analysis of the M1 markers HLA-DR and CD16 and the M2 markers <t>CD206</t> and CD163 on ( a ) M0, ( b ) polarized M(IFN-γ/LPS), and ( c ) polarized M(IL-10) macrophages. Macrophages (7 × 10 5 cells per mL) were stimulated or not with 10 −8 M NPY in the presence or absence of LPS in complete medium for 24 h and then analyzed for surface marker expressions by flow cytometry. Histograms show the percentages of positive cells (%) and the mean fluorescence intensity (MFI). Results are expressed as mean value ± SD of 4 independent experiments. Significance was determined by one-way ANOVA followed by Tukey’s post hoc analysis; *: p < 0.05, **: p < 0.01.
Pe Conjugated Anti Human Cd206/Cd163, supplied by AAT Bioquest, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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90
Dakewe Biotech Co anti-cd206-pe
Flow cytometric analysis of the M1 markers HLA-DR and CD16 and the M2 markers <t>CD206</t> and CD163 on ( a ) M0, ( b ) polarized M(IFN-γ/LPS), and ( c ) polarized M(IL-10) macrophages. Macrophages (7 × 10 5 cells per mL) were stimulated or not with 10 −8 M NPY in the presence or absence of LPS in complete medium for 24 h and then analyzed for surface marker expressions by flow cytometry. Histograms show the percentages of positive cells (%) and the mean fluorescence intensity (MFI). Results are expressed as mean value ± SD of 4 independent experiments. Significance was determined by one-way ANOVA followed by Tukey’s post hoc analysis; *: p < 0.05, **: p < 0.01.
Anti Cd206 Pe, supplied by Dakewe Biotech Co, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Image Search Results


Flow cytometric analysis of the M1 markers HLA-DR and CD16 and the M2 markers CD206 and CD163 on ( a ) M0, ( b ) polarized M(IFN-γ/LPS), and ( c ) polarized M(IL-10) macrophages. Macrophages (7 × 10 5 cells per mL) were stimulated or not with 10 −8 M NPY in the presence or absence of LPS in complete medium for 24 h and then analyzed for surface marker expressions by flow cytometry. Histograms show the percentages of positive cells (%) and the mean fluorescence intensity (MFI). Results are expressed as mean value ± SD of 4 independent experiments. Significance was determined by one-way ANOVA followed by Tukey’s post hoc analysis; *: p < 0.05, **: p < 0.01.

Journal: International Journal of Molecular Sciences

Article Title: Neuropeptide Y Promotes Human M2 Macrophage Polarization and Enhances p62/SQSTM1-Dependent Autophagy and NRF2 Activation

doi: 10.3390/ijms232113009

Figure Lengend Snippet: Flow cytometric analysis of the M1 markers HLA-DR and CD16 and the M2 markers CD206 and CD163 on ( a ) M0, ( b ) polarized M(IFN-γ/LPS), and ( c ) polarized M(IL-10) macrophages. Macrophages (7 × 10 5 cells per mL) were stimulated or not with 10 −8 M NPY in the presence or absence of LPS in complete medium for 24 h and then analyzed for surface marker expressions by flow cytometry. Histograms show the percentages of positive cells (%) and the mean fluorescence intensity (MFI). Results are expressed as mean value ± SD of 4 independent experiments. Significance was determined by one-way ANOVA followed by Tukey’s post hoc analysis; *: p < 0.05, **: p < 0.01.

Article Snippet: To determine macrophage phenotypic surface markers, macrophages were stained with the following monoclonal antibodies (mAbs): phycoerythrin (PE)-CD163, fluorescein isothiocyanate (FITC)-CD206 and PE-Vio770-CD206 mAbs (Miltenyi Biotec), allophycocyanin (APC)-CD16 and APC-Alexa Fluor 750-HLA-DR (clone Immu357) mAbs (Beckman Coulter, Lane Cove, Australia), PE-CD1a and FITC-CD14 mAbs, or with isotype-matched control mAbs from PharMingen (PharMingen, San Diego, CA, USA) for 30 min at 4 °C.

Techniques: Marker, Flow Cytometry, Fluorescence