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tonbo fix permeabilization solution  (Cytek Biosciences)


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    Structured Review

    Cytek Biosciences tonbo fix permeabilization solution
    Tonbo Fix Permeabilization Solution, supplied by Cytek Biosciences, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/fixation+buffer+(fix/Fixation+Buffer/pmc12355481-57-22-22
    Average 95 stars, based on 1 article reviews
    tonbo fix permeabilization solution - by Bioz Stars, 2026-09
    95/100 stars

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    Related Articles

    Incubation:

    Article Title: Mitochondrial protein OPA1 is required for the expansion of effector CD8 T cells.
    Article Snippet: Article Mitochondrial protein OPA1 is required for the expansion of effector CD8 T cells

    Article Title: Mitochondrial protein OPA1 is required for the expansion of effector CD8 T cells
    Article Snippet: .. After washing, cells were incubated in fix/perm buffer (Tonbo) for 20 min, washed twice in perm buffer (Tonbo), and incubated with anti-puromycin-PE antibody (Biolegend) for 30 min-overnight. ..

    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: 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: 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: Incretin triple agonist retatrutide (LY3437943) alleviates obesity-associated cancer progression
    Article Snippet: Following red blood cell lysis (BioLegend), viability was determined by staining with Ghost dye (Tonbo Biosciences, Inc.) followed by FcR-blocking (Tonbo Biosciences, Inc.). .. Cells were stained with fluorescently labeled antibodies and fixed in Perm/fix buffer (Tonbo Biosciences Inc.). .. Stained cells were analyzed using a Bio-Rad ZE5 flow cytometer at the UTHSC Flow Cytometry and Cell Sorting Core.

    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: The gut microbiome enhances breast cancer immunotherapy following bariatric surgery.
    Article Snippet: In all studies, following red blood cell lysis (BioLegend), viability was determined by staining with Ghost dye (Tonbo Biosciences, Inc.) followed by FcR-blocking (Tonbo Biosciences, Inc.). .. Cells were stained with fluorescently labeled antibodies and fixed in Perm/fix buffer (Tonbo Biosciences Inc.). ..

    Labeling:

    Article Title: Incretin triple agonist retatrutide (LY3437943) alleviates obesity-associated cancer progression
    Article Snippet: Following red blood cell lysis (BioLegend), viability was determined by staining with Ghost dye (Tonbo Biosciences, Inc.) followed by FcR-blocking (Tonbo Biosciences, Inc.). .. Cells were stained with fluorescently labeled antibodies and fixed in Perm/fix buffer (Tonbo Biosciences Inc.). .. Stained cells were analyzed using a Bio-Rad ZE5 flow cytometer at the UTHSC Flow Cytometry and Cell Sorting Core.

    Article Title: The gut microbiome enhances breast cancer immunotherapy following bariatric surgery.
    Article Snippet: In all studies, following red blood cell lysis (BioLegend), viability was determined by staining with Ghost dye (Tonbo Biosciences, Inc.) followed by FcR-blocking (Tonbo Biosciences, Inc.). .. Cells were stained with fluorescently labeled antibodies and fixed in Perm/fix buffer (Tonbo Biosciences Inc.). ..

    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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