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flow cytometry staining buffer  (Thermo Fisher)


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    Structured Review

    Thermo Fisher flow cytometry staining buffer
    Flow <t>cytometry</t> for MACS-isolated microglia purity (A and B) Total CD11b-positive cells from MACS columns; (C) Cell viability assessed by Zombie Red staining; (D) Infiltrating leukocytes, including neutrophils (Ly6G+) and T lymphocytes (CD3+); (E) Proportions of microglia (CD11b+CD45low) versus monocytes/border-associated macrophages (CD11b+CD45high); (F) Proportion of resting (homeostatic) microglia identified as CD11b+TMEM119+ cells.
    Flow Cytometry Staining Buffer, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/staining+buffer/Matrix+DeepWell+Storage+Blocks/pmc13068824-328-4-9
    Average 97 stars, based on 1 article reviews
    flow cytometry staining buffer - by Bioz Stars, 2026-09
    97/100 stars

    Images

    1) Product Images from "Protocol for isolating and culturing microglia from the adult mouse brain using a magnetic-activated cell sorting system"

    Article Title: Protocol for isolating and culturing microglia from the adult mouse brain using a magnetic-activated cell sorting system

    Journal: STAR Protocols

    doi: 10.1016/j.xpro.2026.104471

    Flow cytometry for MACS-isolated microglia purity (A and B) Total CD11b-positive cells from MACS columns; (C) Cell viability assessed by Zombie Red staining; (D) Infiltrating leukocytes, including neutrophils (Ly6G+) and T lymphocytes (CD3+); (E) Proportions of microglia (CD11b+CD45low) versus monocytes/border-associated macrophages (CD11b+CD45high); (F) Proportion of resting (homeostatic) microglia identified as CD11b+TMEM119+ cells.
    Figure Legend Snippet: Flow cytometry for MACS-isolated microglia purity (A and B) Total CD11b-positive cells from MACS columns; (C) Cell viability assessed by Zombie Red staining; (D) Infiltrating leukocytes, including neutrophils (Ly6G+) and T lymphocytes (CD3+); (E) Proportions of microglia (CD11b+CD45low) versus monocytes/border-associated macrophages (CD11b+CD45high); (F) Proportion of resting (homeostatic) microglia identified as CD11b+TMEM119+ cells.

    Techniques Used: Flow Cytometry, Isolation, Staining

    Related Articles

    Incubation:

    Article Title: RIG-I–Adjuvanted Immunogen Elicited T-Cell Immunity Controls Trypanosoma cruzi, Chagasic Cardiomyopathy, and Left Ventricular Dysfunction
    Article Snippet: .. Briefly, splenocytes were incubated for 15 minutes with Fc block (antiCD16/CD32) in brilliant-stain buffer (BD Biosciences) and washed with staining buffer (00-4222-26; eBioscience). ..

    Article Title: RIG-I–Adjuvanted Immunogen Elicited T-Cell Immunity Controls Trypanosoma cruzi , Chagasic Cardiomyopathy, and Left Ventricular Dysfunction
    Article Snippet: .. Briefly, splenocytes were incubated for 15 minutes with Fc block (anti-CD16/CD32) in brilliant-stain buffer (BD Biosciences) and washed with staining buffer (00-4222-26; eBioscience). ..

    Article Title: Enterococcus faecalis biofilm rewires neutrophil metabolism to suppress antimicrobial functions
    Article Snippet: .. Samples were incubated overnight at 4°C with rabbit anti-histone H3 (citrulline R2 + R8 + R17) (1:500; Cat. Nr. ab5103, abcam) or goat anti-human/mouse myeloperoxidase (1:40; AF3667, R&D Systems) in staining buffer (1% goat serum, 1% BSA, 0.05% Triton X-100 in PBS), washed three times, and incubated with fluorophore-conjugated secondary antibodies goat anti-rabbit IgG Alexa Fluor 488 (1:1000; Cat. Nr. A11034, Thermo Fisher Scientific) or donkey anti-goat IgG Alexa Fluor 568 (1:1000; Cat. Nr. A11057, Thermo Fisher Scientific) respectively for 1 h at RT in the dark. .. F-actin was stained with Alexa Fluor 588-phalloidin (1:500; Thermo Fisher Scientific) for 30 min at RT and nuclei with 4’,6-diamidino-2-phenylindole (DAPI) (1:500, stock concentration 5 mg/mL, Thermo Fisher Scientific) for 5 min at RT.

    Article Title: Peripheral immune cell subsets as potential predictors of benefit from immune checkpoint blockade therapy in small cell lung cancer
    Article Snippet: Cells were resuspended in Fixable Violet Viability kit (Thermo Fisher Scientific) following manufacturer ́s protocol, incubated for 30 minutes at 4°C in the dark and washed twice with phosphate buffered saline (PBS) 1X (Gibco, Thermo Fisher Scientific). .. For each antibody configuration, one million cells per panel were incubated with 1:100 dilution of Fc receptor blocking solution containing purified monoclonal anti-CD16 antibody (CB16) (eBioscience) in staining buffer (PBS 1X with 2% bovine serum albumin (Sigma-Aldrich) and 2 mM EDTA (Sigma-Aldrich)) for 15 minutes at 4°C. ..

    Article Title: The dynamics of mutational selection in cutaneous squamous carcinogenesis.
    Article Snippet: .. Wholemount samples were then incubated with p53 antibody (1:500) in staining buffer overnight, washed three times in PBS/0.2% Tween-20, incubated with fluorchrome-conjugated secondary antibodies (Invitrogen, A31572) for 2h at room temperature and washed as before. .. Epidermal wholemounts were dissected into 1-2mm2 grids and DNA extracted using QIAMP DNA microkit (Qiagen) by digesting overnight and following manufacturer’s instructions.

    Blocking Assay:

    Article Title: RIG-I–Adjuvanted Immunogen Elicited T-Cell Immunity Controls Trypanosoma cruzi, Chagasic Cardiomyopathy, and Left Ventricular Dysfunction
    Article Snippet: .. Briefly, splenocytes were incubated for 15 minutes with Fc block (antiCD16/CD32) in brilliant-stain buffer (BD Biosciences) and washed with staining buffer (00-4222-26; eBioscience). ..

    Article Title: RIG-I–Adjuvanted Immunogen Elicited T-Cell Immunity Controls Trypanosoma cruzi , Chagasic Cardiomyopathy, and Left Ventricular Dysfunction
    Article Snippet: .. Briefly, splenocytes were incubated for 15 minutes with Fc block (anti-CD16/CD32) in brilliant-stain buffer (BD Biosciences) and washed with staining buffer (00-4222-26; eBioscience). ..

    Article Title: Peripheral immune cell subsets as potential predictors of benefit from immune checkpoint blockade therapy in small cell lung cancer
    Article Snippet: Cells were resuspended in Fixable Violet Viability kit (Thermo Fisher Scientific) following manufacturer ́s protocol, incubated for 30 minutes at 4°C in the dark and washed twice with phosphate buffered saline (PBS) 1X (Gibco, Thermo Fisher Scientific). .. For each antibody configuration, one million cells per panel were incubated with 1:100 dilution of Fc receptor blocking solution containing purified monoclonal anti-CD16 antibody (CB16) (eBioscience) in staining buffer (PBS 1X with 2% bovine serum albumin (Sigma-Aldrich) and 2 mM EDTA (Sigma-Aldrich)) for 15 minutes at 4°C. ..

    Article Title: Enantiomer-dependent and modification-free DNA matrix as an adjuvant for subunit vaccines against SARS-CoV-2 or pneumococcal infections.
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    Staining:

    Article Title: RIG-I–Adjuvanted Immunogen Elicited T-Cell Immunity Controls Trypanosoma cruzi, Chagasic Cardiomyopathy, and Left Ventricular Dysfunction
    Article Snippet: .. Briefly, splenocytes were incubated for 15 minutes with Fc block (antiCD16/CD32) in brilliant-stain buffer (BD Biosciences) and washed with staining buffer (00-4222-26; eBioscience). ..

    Article Title: IL-15 promotes immune escape, invasion, and metastasis of pancreatic cancer by upregulating PD-L1 expression via the JAK1/STAT1/IRF1 pathway.
    Article Snippet: .. Flow cytometry: PD-L1 staining CFPAC-1/BxPC-3 cells were digested into single cells and adjusted to 1×106 cells/mL in staining buffer (00-4222-26, Thermo Fisher). .. A 100 μL cell suspension was mixed with 5 μL PD-L1 antibody (F1127403, MultiSciences, Hangzhou, China) and incubated for 60 min; the cells were then detected by the BD FACSVerse (BD Biosciences, Franklin Lakes, NJ, USA) and analyzed via FlowJo.

    Article Title: RIG-I–Adjuvanted Immunogen Elicited T-Cell Immunity Controls Trypanosoma cruzi , Chagasic Cardiomyopathy, and Left Ventricular Dysfunction
    Article Snippet: .. Briefly, splenocytes were incubated for 15 minutes with Fc block (anti-CD16/CD32) in brilliant-stain buffer (BD Biosciences) and washed with staining buffer (00-4222-26; eBioscience). ..

    Article Title: Enterococcus faecalis biofilm rewires neutrophil metabolism to suppress antimicrobial functions
    Article Snippet: .. Samples were incubated overnight at 4°C with rabbit anti-histone H3 (citrulline R2 + R8 + R17) (1:500; Cat. Nr. ab5103, abcam) or goat anti-human/mouse myeloperoxidase (1:40; AF3667, R&D Systems) in staining buffer (1% goat serum, 1% BSA, 0.05% Triton X-100 in PBS), washed three times, and incubated with fluorophore-conjugated secondary antibodies goat anti-rabbit IgG Alexa Fluor 488 (1:1000; Cat. Nr. A11034, Thermo Fisher Scientific) or donkey anti-goat IgG Alexa Fluor 568 (1:1000; Cat. Nr. A11057, Thermo Fisher Scientific) respectively for 1 h at RT in the dark. .. F-actin was stained with Alexa Fluor 588-phalloidin (1:500; Thermo Fisher Scientific) for 30 min at RT and nuclei with 4’,6-diamidino-2-phenylindole (DAPI) (1:500, stock concentration 5 mg/mL, Thermo Fisher Scientific) for 5 min at RT.

    Article Title: Peripheral immune cell subsets as potential predictors of benefit from immune checkpoint blockade therapy in small cell lung cancer
    Article Snippet: Cells were resuspended in Fixable Violet Viability kit (Thermo Fisher Scientific) following manufacturer ́s protocol, incubated for 30 minutes at 4°C in the dark and washed twice with phosphate buffered saline (PBS) 1X (Gibco, Thermo Fisher Scientific). .. For each antibody configuration, one million cells per panel were incubated with 1:100 dilution of Fc receptor blocking solution containing purified monoclonal anti-CD16 antibody (CB16) (eBioscience) in staining buffer (PBS 1X with 2% bovine serum albumin (Sigma-Aldrich) and 2 mM EDTA (Sigma-Aldrich)) for 15 minutes at 4°C. ..

    Article Title: Enantiomer-dependent and modification-free DNA matrix as an adjuvant for subunit vaccines against SARS-CoV-2 or pneumococcal infections.
    Article Snippet: The emergence of novel infectious disease has intensified demand for more advanced vaccine development and more potent adjuvants to enhance immunogenicity.. Here we introduce a dynamic DNA supramolecular matrix assembled from five unmodified, short DNA single strands, serving as a safe, multifaceted adjuvant platform.. This DNA matrix elicits a robust humoral response with minimal adverse effects, generating potent neutralizing antibodies and conferring robust protection against SARS-CoV-2 and Streptococcus pneumoniae infections.

    Article Title: The dynamics of mutational selection in cutaneous squamous carcinogenesis.
    Article Snippet: .. Wholemount samples were then incubated with p53 antibody (1:500) in staining buffer overnight, washed three times in PBS/0.2% Tween-20, incubated with fluorchrome-conjugated secondary antibodies (Invitrogen, A31572) for 2h at room temperature and washed as before. .. Epidermal wholemounts were dissected into 1-2mm2 grids and DNA extracted using QIAMP DNA microkit (Qiagen) by digesting overnight and following manufacturer’s instructions.

    Article Title: AANG: A natural compound formulation for targeting macrophage-myofibroblast transition in non-small-cell lung carcinoma.
    Article Snippet: Sections were blocked with 5 % bovine serum albumin (BSA) and incubated overnight at 4 ◦C with primary antibodies against α-SMA (F3777, Sigma), CD68 (PE-conjugated, sc-20,060, Santa Cruz), Smad7 (FITC-conjugated, sc-365,846, Santa Cruz), and p-Smad3 (sc-517,575, Santa Cruz). .. Antibodies were diluted to be 1:100 in staining buffer (eBioscience 00–4222–57) and applied on the samples at 4 ◦C for overnight. .. The unbounded antibodies were washed out with PBST 3 times followed by detection with Alexa FITC-conjugated secondary antibodies (F-2761, Invitrogen) at 1:1000 dilution.

    Flow Cytometry:

    Article Title: IL-15 promotes immune escape, invasion, and metastasis of pancreatic cancer by upregulating PD-L1 expression via the JAK1/STAT1/IRF1 pathway.
    Article Snippet: .. Flow cytometry: PD-L1 staining CFPAC-1/BxPC-3 cells were digested into single cells and adjusted to 1×106 cells/mL in staining buffer (00-4222-26, Thermo Fisher). .. A 100 μL cell suspension was mixed with 5 μL PD-L1 antibody (F1127403, MultiSciences, Hangzhou, China) and incubated for 60 min; the cells were then detected by the BD FACSVerse (BD Biosciences, Franklin Lakes, NJ, USA) and analyzed via FlowJo.

    Purification:

    Article Title: Peripheral immune cell subsets as potential predictors of benefit from immune checkpoint blockade therapy in small cell lung cancer
    Article Snippet: Cells were resuspended in Fixable Violet Viability kit (Thermo Fisher Scientific) following manufacturer ́s protocol, incubated for 30 minutes at 4°C in the dark and washed twice with phosphate buffered saline (PBS) 1X (Gibco, Thermo Fisher Scientific). .. For each antibody configuration, one million cells per panel were incubated with 1:100 dilution of Fc receptor blocking solution containing purified monoclonal anti-CD16 antibody (CB16) (eBioscience) in staining buffer (PBS 1X with 2% bovine serum albumin (Sigma-Aldrich) and 2 mM EDTA (Sigma-Aldrich)) for 15 minutes at 4°C. ..



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    Image Search Results


    Flow cytometry for MACS-isolated microglia purity (A and B) Total CD11b-positive cells from MACS columns; (C) Cell viability assessed by Zombie Red staining; (D) Infiltrating leukocytes, including neutrophils (Ly6G+) and T lymphocytes (CD3+); (E) Proportions of microglia (CD11b+CD45low) versus monocytes/border-associated macrophages (CD11b+CD45high); (F) Proportion of resting (homeostatic) microglia identified as CD11b+TMEM119+ cells.

    Journal: STAR Protocols

    Article Title: Protocol for isolating and culturing microglia from the adult mouse brain using a magnetic-activated cell sorting system

    doi: 10.1016/j.xpro.2026.104471

    Figure Lengend Snippet: Flow cytometry for MACS-isolated microglia purity (A and B) Total CD11b-positive cells from MACS columns; (C) Cell viability assessed by Zombie Red staining; (D) Infiltrating leukocytes, including neutrophils (Ly6G+) and T lymphocytes (CD3+); (E) Proportions of microglia (CD11b+CD45low) versus monocytes/border-associated macrophages (CD11b+CD45high); (F) Proportion of resting (homeostatic) microglia identified as CD11b+TMEM119+ cells.

    Article Snippet: Note: We use commercial flow cytometry staining buffer from eBioscience (Cat# 00-4222-26), which is PBS-based formulation designed to prevent non-specific antibody binding and maintain cell stability during flow cytometry.

    Techniques: Flow Cytometry, Isolation, Staining