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fixation permeabilization solution  (Cytek Biosciences)


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    Structured Review

    Cytek Biosciences fixation permeabilization solution
    Fixation Permeabilization Solution, supplied by Cytek Biosciences, used in various techniques. Bioz Stars score: 97/100, based on 300 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/fixation+buffer+solution/Foxp3+%2F+Transcription+Factor+Staining+Buffer+Kit/bio_rxiv__2025__10__25__684515-300-11-13
    Average 97 stars, based on 300 article reviews
    fixation permeabilization solution - by Bioz Stars, 2026-09
    97/100 stars

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    Related Articles

    Incubation:

    Article Title: The immune landscape of fetal chorionic villous tissue in term placenta
    Article Snippet: To prevent non-specific binding by myeloid cells, True-Stain Monocyte Block and Human TruStain FcXTM (Fc Receptor Blocking Solution) (BioLegend, San Diego, CA) were also added to the surface staining cocktail (1:20). .. After incubation for 30 minutes at 4°C, the iMGL cell pellet was washed with FACS buffer, fixed for 20 minutes (Tonbo fix/permeabilization solution, 1:3), permeabilized (Tonbo permeabilization buffer), and stained with the following panel of intranuclear antibodies: PU.1, IBA.1, and IRF8 (BioLegend, San Diego, CA) at a ratio of 1:20 overnight at 4°C. .. The next day, stained iMGL were washed with FACS buffer, and were run using an Attune NxT and analyzed on FlowJo 10.10 (Beckton Dickinson, Ashland, OR).

    Article Title: Prenatal opioid exposure and maternal HCV infection impair microglia development and function: A patient-specific in vitro model.
    Article Snippet: Opioids are a class of pain-relieving drugs known to cross the placental and blood brain barriers, exposing the fetus in utero.. Rates of opioid use disorder amongst pregnant individuals in the United States are on the rise, and intravenous routes of opioid administration are highly associated with hepatitis C (HCV) infection.. Newborns with prenatal opioid exposure (POE) are more likely to be small for gestational age and have increased rates of neurodevelopmental delay.

    Article Title: Prenatal opioid exposure and maternal HCV infection impair microglia development and function: a patient-specific in vitro model
    Article Snippet: Thawed UCBMC from newborns of full-term, healthy pregnancies (N=9) or iMGL (N=27, 9 Controls, 9 POE HCV−, and 9 POE HCV+) were thoroughly washed with FACS buffer, and stained with a cocktail of the following surface antibodies at a ratio of 1:20 in 50μl/sample of Brilliant Stain Buffer (BD Biosciences): CD14, HLA-DR, CD16, CX3CR1, CD45, CD11b, P2RY12, TMEM119, TREM2, CD68, CD40, CD163, CD115, and CD86 46 , 47 as well as True-Stain Monocyte Block and Human TruStain FcX TM (Fc Receptor Blocking Solution, BioLegend, 1:20). .. After incubation for 30 minutes at 4°C, UCBMCs or the iMGL cell pellet was washed with FACS buffer, fixed for 2 hours (Tonbo fix/permeabilization solution, 1:3), permeabilized (Tonbo permeabilization buffer), and stained with PU.1, IBA.1, and IRF8 intranuclear antibodies at a ratio of 1:20, overnight 4°C. .. The next day, stained UCBMCs/iMGLs were washed with FACS buffer, ran on the Cytek Aurora flow cytometer (Cytek Biosciences, 5-laser; 355 nm, 405 nm, 488 nm, 561 nm, and 640 nm) using the SpectroFlo Software v2.2.0.2.

    FACS:

    Article Title: The immune landscape of fetal chorionic villous tissue in term placenta
    Article Snippet: To prevent non-specific binding by myeloid cells, True-Stain Monocyte Block and Human TruStain FcXTM (Fc Receptor Blocking Solution) (BioLegend, San Diego, CA) were also added to the surface staining cocktail (1:20). .. After incubation for 30 minutes at 4°C, the iMGL cell pellet was washed with FACS buffer, fixed for 20 minutes (Tonbo fix/permeabilization solution, 1:3), permeabilized (Tonbo permeabilization buffer), and stained with the following panel of intranuclear antibodies: PU.1, IBA.1, and IRF8 (BioLegend, San Diego, CA) at a ratio of 1:20 overnight at 4°C. .. The next day, stained iMGL were washed with FACS buffer, and were run using an Attune NxT and analyzed on FlowJo 10.10 (Beckton Dickinson, Ashland, OR).

    Article Title: Prenatal opioid exposure and maternal HCV infection impair microglia development and function: A patient-specific in vitro model.
    Article Snippet: Opioids are a class of pain-relieving drugs known to cross the placental and blood brain barriers, exposing the fetus in utero.. Rates of opioid use disorder amongst pregnant individuals in the United States are on the rise, and intravenous routes of opioid administration are highly associated with hepatitis C (HCV) infection.. Newborns with prenatal opioid exposure (POE) are more likely to be small for gestational age and have increased rates of neurodevelopmental delay.

    Article Title: Prenatal opioid exposure and maternal HCV infection impair microglia development and function: a patient-specific in vitro model
    Article Snippet: Thawed UCBMC from newborns of full-term, healthy pregnancies (N=9) or iMGL (N=27, 9 Controls, 9 POE HCV−, and 9 POE HCV+) were thoroughly washed with FACS buffer, and stained with a cocktail of the following surface antibodies at a ratio of 1:20 in 50μl/sample of Brilliant Stain Buffer (BD Biosciences): CD14, HLA-DR, CD16, CX3CR1, CD45, CD11b, P2RY12, TMEM119, TREM2, CD68, CD40, CD163, CD115, and CD86 46 , 47 as well as True-Stain Monocyte Block and Human TruStain FcX TM (Fc Receptor Blocking Solution, BioLegend, 1:20). .. After incubation for 30 minutes at 4°C, UCBMCs or the iMGL cell pellet was washed with FACS buffer, fixed for 2 hours (Tonbo fix/permeabilization solution, 1:3), permeabilized (Tonbo permeabilization buffer), and stained with PU.1, IBA.1, and IRF8 intranuclear antibodies at a ratio of 1:20, overnight 4°C. .. The next day, stained UCBMCs/iMGLs were washed with FACS buffer, ran on the Cytek Aurora flow cytometer (Cytek Biosciences, 5-laser; 355 nm, 405 nm, 488 nm, 561 nm, and 640 nm) using the SpectroFlo Software v2.2.0.2.

    Staining:

    Article Title: The immune landscape of fetal chorionic villous tissue in term placenta
    Article Snippet: To prevent non-specific binding by myeloid cells, True-Stain Monocyte Block and Human TruStain FcXTM (Fc Receptor Blocking Solution) (BioLegend, San Diego, CA) were also added to the surface staining cocktail (1:20). .. After incubation for 30 minutes at 4°C, the iMGL cell pellet was washed with FACS buffer, fixed for 20 minutes (Tonbo fix/permeabilization solution, 1:3), permeabilized (Tonbo permeabilization buffer), and stained with the following panel of intranuclear antibodies: PU.1, IBA.1, and IRF8 (BioLegend, San Diego, CA) at a ratio of 1:20 overnight at 4°C. .. The next day, stained iMGL were washed with FACS buffer, and were run using an Attune NxT and analyzed on FlowJo 10.10 (Beckton Dickinson, Ashland, OR).

    Article Title: Prenatal opioid exposure and maternal HCV infection impair microglia development and function: A patient-specific in vitro model.
    Article Snippet: Opioids are a class of pain-relieving drugs known to cross the placental and blood brain barriers, exposing the fetus in utero.. Rates of opioid use disorder amongst pregnant individuals in the United States are on the rise, and intravenous routes of opioid administration are highly associated with hepatitis C (HCV) infection.. Newborns with prenatal opioid exposure (POE) are more likely to be small for gestational age and have increased rates of neurodevelopmental delay.

    Article Title: Prenatal opioid exposure and maternal HCV infection impair microglia development and function: a patient-specific in vitro model
    Article Snippet: Thawed UCBMC from newborns of full-term, healthy pregnancies (N=9) or iMGL (N=27, 9 Controls, 9 POE HCV−, and 9 POE HCV+) were thoroughly washed with FACS buffer, and stained with a cocktail of the following surface antibodies at a ratio of 1:20 in 50μl/sample of Brilliant Stain Buffer (BD Biosciences): CD14, HLA-DR, CD16, CX3CR1, CD45, CD11b, P2RY12, TMEM119, TREM2, CD68, CD40, CD163, CD115, and CD86 46 , 47 as well as True-Stain Monocyte Block and Human TruStain FcX TM (Fc Receptor Blocking Solution, BioLegend, 1:20). .. After incubation for 30 minutes at 4°C, UCBMCs or the iMGL cell pellet was washed with FACS buffer, fixed for 2 hours (Tonbo fix/permeabilization solution, 1:3), permeabilized (Tonbo permeabilization buffer), and stained with PU.1, IBA.1, and IRF8 intranuclear antibodies at a ratio of 1:20, overnight 4°C. .. The next day, stained UCBMCs/iMGLs were washed with FACS buffer, ran on the Cytek Aurora flow cytometer (Cytek Biosciences, 5-laser; 355 nm, 405 nm, 488 nm, 561 nm, and 640 nm) using the SpectroFlo Software v2.2.0.2.

    Article Title: Blocking plasma cell fate enhances antigen-specific presentation by B cells to boost anti-tumor immunity
    Article Snippet: After surface staining, cells were fixed by 4% PFA, followed by permeabilization and staining with Perm/WashTM Buffer (BD Biosciences). .. For intranuclear staining, the Foxp3 Fixation/Permeabilization solution (TONBO Biosciences) was used after surface staining. .. All samples were acquired on BD LSR2 flow cytometer (BD Biosciences), or Aurora spectral flow cytometry (Cytek Biosciences) and data were analyzed using Flowjo software (v10).

    Article Title: Mitochondrial protein OPA1 is required for the expansion of effector CD8 T cells
    Article Snippet: For viability and surface staining, cells were stained in complete media for 10 min at 37°C with Ghost Dye Red 780 (Tonbo) and surface antibodies (1:300, unless noted otherwise) against CD19 (1D3; BD Biosciences), CD8α (53–6.7; BioLegend), CD44 (1:150, IM7; Tonbo), CD45.1 (A20; BioLegend), CD45.2 (104; BioLegend), KLRG1 (2F1/KLRG1; BioLegend), CD127 (1:150, A7R34; BioLegend), and CD98 (RL388; BioLegend). .. After wash with RPMI, cells were fixed and permeabilized for 30 min at RT in FoxP3/Transcription Factor 1x Fix/Perm solution (Tonbo), followed by wash with 1x Flow Cytometry Perm Buffer (Tonbo), and intracellular staining in Perm Buffer for 30 min at RT with an intracellular antibody against GZMB (1:100, QA16A02; BioLegend). ..

    Article Title: Blocking plasma cell fate enhances antigen-specific presentation by B cells to boost anti-tumor immunity.
    Article Snippet: After surface staining, cells were fixed by 4% PFA, followed by permeabilization and staining with Perm/ WashTM Buffer (BD Biosciences). .. For intranuclear staining, the Foxp3 Fixation/Permeabilization solution (TONBO Biosciences) was used after surface staining. .. All samples were acquired on BD LSR2 flow cytometer (BD Biosciences), or Aurora spectral flow cytometry (Cytek Biosciences) and data were analyzed using Flowjo software (v10).

    Article Title: Single-cell proteomics characterization of bone marrow hematopoiesis with distinct Ras pathway lesions
    Article Snippet: .. Cells were then fixed/permed with 100uL fixation solution (FoxP3 Transcription Factor Staining Buffer Kit; Tonbo Biosciences cat. no. TNB-0607KIT) for 20 minutes in the dark. ..

    Magnetic Cell Separation:

    Article Title: Tumor cell dissemination is facilitated through regulatory T cell-driven extracellular matrix remodeling
    Article Snippet: Samples were stained with AF-700-conjugated anti-CD45 antibody (30-F11 clone, Thermo 56- 0451-82, 1:125) in MACS buffer for 20 minutes, covered on ice. .. Wells were washed with MACS buffer and resuspended in 100uL of fixation/permeabilization solution (TONBO, TNB-0607-KIT) for 40 minutes, covered on ice. .. Cells were then permeabilized with 1X Perm Buffer (TONBO, TNB- 0607-KIT), for 20 minutes, covered on ice.

    Flow Cytometry:

    Article Title: Mitochondrial protein OPA1 is required for the expansion of effector CD8 T cells
    Article Snippet: For viability and surface staining, cells were stained in complete media for 10 min at 37°C with Ghost Dye Red 780 (Tonbo) and surface antibodies (1:300, unless noted otherwise) against CD19 (1D3; BD Biosciences), CD8α (53–6.7; BioLegend), CD44 (1:150, IM7; Tonbo), CD45.1 (A20; BioLegend), CD45.2 (104; BioLegend), KLRG1 (2F1/KLRG1; BioLegend), CD127 (1:150, A7R34; BioLegend), and CD98 (RL388; BioLegend). .. After wash with RPMI, cells were fixed and permeabilized for 30 min at RT in FoxP3/Transcription Factor 1x Fix/Perm solution (Tonbo), followed by wash with 1x Flow Cytometry Perm Buffer (Tonbo), and intracellular staining in Perm Buffer for 30 min at RT with an intracellular antibody against GZMB (1:100, QA16A02; BioLegend). ..



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