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fc block  (Miltenyi Biotec)


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    Structured Review

    Miltenyi Biotec fc block
    Fc Block, supplied by Miltenyi Biotec, used in various techniques. Bioz Stars score: 97/100, based on 1388 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/fc+block/FcR+Blocking+Reagent%2C+mouse/10__1016_slash_j__gendis__2026__102441-385-9-13
    Average 97 stars, based on 1388 article reviews
    fc block - by Bioz Stars, 2026-11
    97/100 stars

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    Related Articles

    Fluorescence:

    Article Title: citrOgen: a synthesis-free polysaccharide and protein antigen-presentation to antibody-induction platform
    Article Snippet: Cells were then incubated 5 min at RT with 50 μg/mL DNase I (#11284932001, Sigma) to digest extracellular DNA and passed through a 70-μm cell strainer on ice to ensure a single-cell suspension, pooling samples from the same group and rinsing with 20 mL of cold DPBS. .. All steps from here onwards were performed on ice/at 4 °C to maintain cell viability. cIECs were counted using trypan blue to exclude dead cells and ~1 × 10 7 live cells were centrifuged, resuspended in fluorescence-activated cell sorter (FACS) buffer (5% FBS, 2 mM EDTA in DPBS) supplemented with Fc block (#130-092-575, Miltenyi Biotec) and incubated for 10 min. .. Samples were then incubated with FACS buffer containing anti-CR (1:1000) for 20 min, washed twice in and then incubated with EpCAM-APC (1:100) and phycoerythrin (PE) anti-rabbit IgG (Supplementary Data ) for 40 min, washed, and fixed in 1% paraformaldehyde in PBS prior to acquisition on a BD LSRFortessa cell analyser with BD FACSDiva v9.0 Software (BD Biosciences).

    Article Title: citrOgen: a synthesis-free polysaccharide and protein antigen-presentation to antibody-induction platform.
    Article Snippet: Cells were then incubated 5min at RT with 50 μg/mL DNase I (#11284932001, Sigma) to digest extracellular DNA and passed through a 70-μm cell strainer on ice to ensure a single-cell suspension, pooling samples from the same group and rinsing with 20mL of cold DPBS. .. All steps from here onwards were performed on ice/at 4 °C tomaintain cell viability. cIECs were counted using trypan blue to exclude dead cells and ~1 × 107 live cells were centrifuged, resuspended in fluorescence-activated cell sorter (FACS) buffer (5% FBS, 2mMEDTA in DPBS) supplemented with Fc block (#130-092-575, Miltenyi Biotec) and incubated for 10min. .. Samples were then incubated with FACS buffer containing anti-CR (1:1000) for 20min, washed twice in and then incubated with EpCAMAPC (1:100) and phycoerythrin (PE) anti-rabbit IgG (Supplementary Data 3) for 40min, washed, and fixed in 1% paraformaldehyde in PBS prior to acquisition on a BD LSRFortessa cell analyser with BD FACSDiva v9.0 Software (BD Biosciences).

    FACS:

    Article Title: citrOgen: a synthesis-free polysaccharide and protein antigen-presentation to antibody-induction platform
    Article Snippet: Cells were then incubated 5 min at RT with 50 μg/mL DNase I (#11284932001, Sigma) to digest extracellular DNA and passed through a 70-μm cell strainer on ice to ensure a single-cell suspension, pooling samples from the same group and rinsing with 20 mL of cold DPBS. .. All steps from here onwards were performed on ice/at 4 °C to maintain cell viability. cIECs were counted using trypan blue to exclude dead cells and ~1 × 10 7 live cells were centrifuged, resuspended in fluorescence-activated cell sorter (FACS) buffer (5% FBS, 2 mM EDTA in DPBS) supplemented with Fc block (#130-092-575, Miltenyi Biotec) and incubated for 10 min. .. Samples were then incubated with FACS buffer containing anti-CR (1:1000) for 20 min, washed twice in and then incubated with EpCAM-APC (1:100) and phycoerythrin (PE) anti-rabbit IgG (Supplementary Data ) for 40 min, washed, and fixed in 1% paraformaldehyde in PBS prior to acquisition on a BD LSRFortessa cell analyser with BD FACSDiva v9.0 Software (BD Biosciences).

    Article Title: Conserved T cell receptor usage underpins recognition of CD1c presenting a mycobacterial lipid
    Article Snippet: For PBMC staining, cells were first incubated in 50 nM dasatinib (STEMCELL Technologies 73082) in PBS for 30 min at 37°C. .. After washing in FACS buffer (PBS supplemented with 2% FBS and 2μg/ml DNAse, Roche 10104159001), cells were then blocked in FACS buffer containing anti-CD36 (10 μg/ml, clone 5-721, Biolegend 336202) and Fc-block (1:50, Miltenyi 130-059-901) for 15 min at 4°C. .. CD1c and CD1d tetramers (produced in-house as previously described( ) made from streptavidin phycoerythrin (PE; Becton Dickinson 554061) were the added directly to the cells at a final concentration of 1 μg/ml and incubated for a further 30 min at RT.

    Article Title: citrOgen: a synthesis-free polysaccharide and protein antigen-presentation to antibody-induction platform.
    Article Snippet: Cells were then incubated 5min at RT with 50 μg/mL DNase I (#11284932001, Sigma) to digest extracellular DNA and passed through a 70-μm cell strainer on ice to ensure a single-cell suspension, pooling samples from the same group and rinsing with 20mL of cold DPBS. .. All steps from here onwards were performed on ice/at 4 °C tomaintain cell viability. cIECs were counted using trypan blue to exclude dead cells and ~1 × 107 live cells were centrifuged, resuspended in fluorescence-activated cell sorter (FACS) buffer (5% FBS, 2mMEDTA in DPBS) supplemented with Fc block (#130-092-575, Miltenyi Biotec) and incubated for 10min. .. Samples were then incubated with FACS buffer containing anti-CR (1:1000) for 20min, washed twice in and then incubated with EpCAMAPC (1:100) and phycoerythrin (PE) anti-rabbit IgG (Supplementary Data 3) for 40min, washed, and fixed in 1% paraformaldehyde in PBS prior to acquisition on a BD LSRFortessa cell analyser with BD FACSDiva v9.0 Software (BD Biosciences).

    Article Title: Transferrin receptor-mediated transport at the blood-brain barrier is elevated during early development and maintained across aging and in an Alzheimer’s mouse model
    Article Snippet: .. Cells were then blocked with 1:10 FC block (Miltenyi 130-092-575) for 15 minutes at 4°C, followed by a 30 minute incubation of a FACS antibody mix (Ghost Dye-v450 (Tonbo 13-0863-T500; 1:1,000), CD45-PE-Cy7 (Biolegend 103114; 1:200), CD31-PE-CF594 (BD 563616; 1:75), CD11b-APC-Cy7 (Tonbo 25-01120-U100; 1:100), Thy1-A488 (R&D FAB7335G; 1:100), ACSA2-PE (Miltenyi 130-123-284; 1:100), O-1-APC (Invitrogen 50-6506-80; 1:100)) at 4°C protected from light. ..

    Blocking Assay:

    Article Title: citrOgen: a synthesis-free polysaccharide and protein antigen-presentation to antibody-induction platform
    Article Snippet: Cells were then incubated 5 min at RT with 50 μg/mL DNase I (#11284932001, Sigma) to digest extracellular DNA and passed through a 70-μm cell strainer on ice to ensure a single-cell suspension, pooling samples from the same group and rinsing with 20 mL of cold DPBS. .. All steps from here onwards were performed on ice/at 4 °C to maintain cell viability. cIECs were counted using trypan blue to exclude dead cells and ~1 × 10 7 live cells were centrifuged, resuspended in fluorescence-activated cell sorter (FACS) buffer (5% FBS, 2 mM EDTA in DPBS) supplemented with Fc block (#130-092-575, Miltenyi Biotec) and incubated for 10 min. .. Samples were then incubated with FACS buffer containing anti-CR (1:1000) for 20 min, washed twice in and then incubated with EpCAM-APC (1:100) and phycoerythrin (PE) anti-rabbit IgG (Supplementary Data ) for 40 min, washed, and fixed in 1% paraformaldehyde in PBS prior to acquisition on a BD LSRFortessa cell analyser with BD FACSDiva v9.0 Software (BD Biosciences).

    Article Title: Pparg activation-mediated lipid metabolism reprogramming confers an invasive phenotype and immune evasion in early-onset colorectal cancer
    Article Snippet: .. To block non-specific binding, cells were 872 incubated with Fc block (anti-CD16/CD32, 130-092-575, Miltenyi) at 4 °C for 15 873 min. Dead cells were discriminated using LIVE/DEAD Fixable Near-IR viability dye 874 (L34975, ThermoFisher) following the manufacturer's protocol. .. 875 876 Surface staining was subsequently performed: cells were incubated with fluorophore-877 conjugated primary antibodies diluted in FACS buffer at 4 °C in the dark for 30 min. 878 The antibodies included CD8 (ab237709, Abcam, 1:500), PD-1 (clone J43.1, 1:400), 879 TIM-3 (clone RMT3-23, 1:100), and LAG-3 (clone 4-10-C9, 1:100).

    Article Title: An epigenetic switch in vascular phenotype augments anti-tumor immunity.
    Article Snippet: .. Cell suspensions were first incubated with Live-or-Dye viability dye (Biotium 32,002), followed by Fc block (Miltenyi 130-092-575) for 10 min on ice. .. Cells were then stained with PE-conjugated CD31 (BD 553373) and APC-conjugated CD45 (BD 559864) for 30 min on ice.

    Article Title: citrOgen: a synthesis-free polysaccharide and protein antigen-presentation to antibody-induction platform.
    Article Snippet: Cells were then incubated 5min at RT with 50 μg/mL DNase I (#11284932001, Sigma) to digest extracellular DNA and passed through a 70-μm cell strainer on ice to ensure a single-cell suspension, pooling samples from the same group and rinsing with 20mL of cold DPBS. .. All steps from here onwards were performed on ice/at 4 °C tomaintain cell viability. cIECs were counted using trypan blue to exclude dead cells and ~1 × 107 live cells were centrifuged, resuspended in fluorescence-activated cell sorter (FACS) buffer (5% FBS, 2mMEDTA in DPBS) supplemented with Fc block (#130-092-575, Miltenyi Biotec) and incubated for 10min. .. Samples were then incubated with FACS buffer containing anti-CR (1:1000) for 20min, washed twice in and then incubated with EpCAMAPC (1:100) and phycoerythrin (PE) anti-rabbit IgG (Supplementary Data 3) for 40min, washed, and fixed in 1% paraformaldehyde in PBS prior to acquisition on a BD LSRFortessa cell analyser with BD FACSDiva v9.0 Software (BD Biosciences).

    Article Title: An epigenetic switch in vascular phenotype augments anti-tumor immunity
    Article Snippet: Tumors were digested at 37 °C for 30–45 min with agitation (120 rpm) and processed on a GentleMACS Dissociator using program m_imptumor_02 to achieve single-cell suspensions. .. Cell suspensions were first incubated with Live-or-Dye viability dye (Biotium 32002), followed by Fc block (Miltenyi 130-092-575) for 10 min on ice. .. Cell suspensions were first incubated with Live-or-Dye viability dye (Biotium 32002), followed by Fc block (Miltenyi 130-092-575) for 10 min on ice.

    Article Title: Transferrin receptor-mediated transport at the blood-brain barrier is elevated during early development and maintained across aging and in an Alzheimer’s mouse model
    Article Snippet: .. Cells were then blocked with 1:10 FC block (Miltenyi 130-092-575) for 15 minutes at 4°C, followed by a 30 minute incubation of a FACS antibody mix (Ghost Dye-v450 (Tonbo 13-0863-T500; 1:1,000), CD45-PE-Cy7 (Biolegend 103114; 1:200), CD31-PE-CF594 (BD 563616; 1:75), CD11b-APC-Cy7 (Tonbo 25-01120-U100; 1:100), Thy1-A488 (R&D FAB7335G; 1:100), ACSA2-PE (Miltenyi 130-123-284; 1:100), O-1-APC (Invitrogen 50-6506-80; 1:100)) at 4°C protected from light. ..

    Incubation:

    Article Title: citrOgen: a synthesis-free polysaccharide and protein antigen-presentation to antibody-induction platform
    Article Snippet: Cells were then incubated 5 min at RT with 50 μg/mL DNase I (#11284932001, Sigma) to digest extracellular DNA and passed through a 70-μm cell strainer on ice to ensure a single-cell suspension, pooling samples from the same group and rinsing with 20 mL of cold DPBS. .. All steps from here onwards were performed on ice/at 4 °C to maintain cell viability. cIECs were counted using trypan blue to exclude dead cells and ~1 × 10 7 live cells were centrifuged, resuspended in fluorescence-activated cell sorter (FACS) buffer (5% FBS, 2 mM EDTA in DPBS) supplemented with Fc block (#130-092-575, Miltenyi Biotec) and incubated for 10 min. .. Samples were then incubated with FACS buffer containing anti-CR (1:1000) for 20 min, washed twice in and then incubated with EpCAM-APC (1:100) and phycoerythrin (PE) anti-rabbit IgG (Supplementary Data ) for 40 min, washed, and fixed in 1% paraformaldehyde in PBS prior to acquisition on a BD LSRFortessa cell analyser with BD FACSDiva v9.0 Software (BD Biosciences).

    Article Title: Pparg activation-mediated lipid metabolism reprogramming confers an invasive phenotype and immune evasion in early-onset colorectal cancer
    Article Snippet: .. To block non-specific binding, cells were 872 incubated with Fc block (anti-CD16/CD32, 130-092-575, Miltenyi) at 4 °C for 15 873 min. Dead cells were discriminated using LIVE/DEAD Fixable Near-IR viability dye 874 (L34975, ThermoFisher) following the manufacturer's protocol. .. 875 876 Surface staining was subsequently performed: cells were incubated with fluorophore-877 conjugated primary antibodies diluted in FACS buffer at 4 °C in the dark for 30 min. 878 The antibodies included CD8 (ab237709, Abcam, 1:500), PD-1 (clone J43.1, 1:400), 879 TIM-3 (clone RMT3-23, 1:100), and LAG-3 (clone 4-10-C9, 1:100).

    Article Title: Biomimetic 3D-Bioprinted organoids of thymic epithelial tumors for translational drug screening and biomarker identification
    Article Snippet: .. The cells were incubated at room temperature for 10-15 min with FC-block (130-091-935,Miltenyi Biotec) to reduce nonspecific staining. .. Fluorescently labeled 7AAD (420404,Biolegend), CD45 (368512,Biolegend), CD326 (369816,Biolegend),CD8 (344704,Biolegend) and CD3 (317342,Biolegend) antibodiewere added sequentially, followed by 30-min incubation in the dark.

    Article Title: An epigenetic switch in vascular phenotype augments anti-tumor immunity.
    Article Snippet: .. Cell suspensions were first incubated with Live-or-Dye viability dye (Biotium 32,002), followed by Fc block (Miltenyi 130-092-575) for 10 min on ice. .. Cells were then stained with PE-conjugated CD31 (BD 553373) and APC-conjugated CD45 (BD 559864) for 30 min on ice.

    Article Title: citrOgen: a synthesis-free polysaccharide and protein antigen-presentation to antibody-induction platform.
    Article Snippet: Cells were then incubated 5min at RT with 50 μg/mL DNase I (#11284932001, Sigma) to digest extracellular DNA and passed through a 70-μm cell strainer on ice to ensure a single-cell suspension, pooling samples from the same group and rinsing with 20mL of cold DPBS. .. All steps from here onwards were performed on ice/at 4 °C tomaintain cell viability. cIECs were counted using trypan blue to exclude dead cells and ~1 × 107 live cells were centrifuged, resuspended in fluorescence-activated cell sorter (FACS) buffer (5% FBS, 2mMEDTA in DPBS) supplemented with Fc block (#130-092-575, Miltenyi Biotec) and incubated for 10min. .. Samples were then incubated with FACS buffer containing anti-CR (1:1000) for 20min, washed twice in and then incubated with EpCAMAPC (1:100) and phycoerythrin (PE) anti-rabbit IgG (Supplementary Data 3) for 40min, washed, and fixed in 1% paraformaldehyde in PBS prior to acquisition on a BD LSRFortessa cell analyser with BD FACSDiva v9.0 Software (BD Biosciences).

    Article Title: An epigenetic switch in vascular phenotype augments anti-tumor immunity
    Article Snippet: Tumors were digested at 37 °C for 30–45 min with agitation (120 rpm) and processed on a GentleMACS Dissociator using program m_imptumor_02 to achieve single-cell suspensions. .. Cell suspensions were first incubated with Live-or-Dye viability dye (Biotium 32002), followed by Fc block (Miltenyi 130-092-575) for 10 min on ice. .. Cell suspensions were first incubated with Live-or-Dye viability dye (Biotium 32002), followed by Fc block (Miltenyi 130-092-575) for 10 min on ice.

    Article Title: Transferrin receptor-mediated transport at the blood-brain barrier is elevated during early development and maintained across aging and in an Alzheimer’s mouse model
    Article Snippet: .. Cells were then blocked with 1:10 FC block (Miltenyi 130-092-575) for 15 minutes at 4°C, followed by a 30 minute incubation of a FACS antibody mix (Ghost Dye-v450 (Tonbo 13-0863-T500; 1:1,000), CD45-PE-Cy7 (Biolegend 103114; 1:200), CD31-PE-CF594 (BD 563616; 1:75), CD11b-APC-Cy7 (Tonbo 25-01120-U100; 1:100), Thy1-A488 (R&D FAB7335G; 1:100), ACSA2-PE (Miltenyi 130-123-284; 1:100), O-1-APC (Invitrogen 50-6506-80; 1:100)) at 4°C protected from light. ..

    Nonspecific Binding:

    Article Title: Pparg activation-mediated lipid metabolism reprogramming confers an invasive phenotype and immune evasion in early-onset colorectal cancer
    Article Snippet: .. To block non-specific binding, cells were 872 incubated with Fc block (anti-CD16/CD32, 130-092-575, Miltenyi) at 4 °C for 15 873 min. Dead cells were discriminated using LIVE/DEAD Fixable Near-IR viability dye 874 (L34975, ThermoFisher) following the manufacturer's protocol. .. 875 876 Surface staining was subsequently performed: cells were incubated with fluorophore-877 conjugated primary antibodies diluted in FACS buffer at 4 °C in the dark for 30 min. 878 The antibodies included CD8 (ab237709, Abcam, 1:500), PD-1 (clone J43.1, 1:400), 879 TIM-3 (clone RMT3-23, 1:100), and LAG-3 (clone 4-10-C9, 1:100).

    Flow Cytometry:

    Article Title: Biomimetic 3D-Bioprinted organoids of thymic epithelial tumors for translational drug screening and biomarker identification
    Article Snippet: .. The cells were incubated at room temperature for 10-15 min with FC-block (130-091-935,Miltenyi Biotec) to reduce nonspecific staining. .. Fluorescently labeled 7AAD (420404,Biolegend), CD45 (368512,Biolegend), CD326 (369816,Biolegend),CD8 (344704,Biolegend) and CD3 (317342,Biolegend) antibodiewere added sequentially, followed by 30-min incubation in the dark.

    Staining:

    Article Title: Biomimetic 3D-Bioprinted organoids of thymic epithelial tumors for translational drug screening and biomarker identification
    Article Snippet: .. The cells were incubated at room temperature for 10-15 min with FC-block (130-091-935,Miltenyi Biotec) to reduce nonspecific staining. .. Fluorescently labeled 7AAD (420404,Biolegend), CD45 (368512,Biolegend), CD326 (369816,Biolegend),CD8 (344704,Biolegend) and CD3 (317342,Biolegend) antibodiewere added sequentially, followed by 30-min incubation in the dark.



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