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permeabilization buffer set  (Multi Sciences (Lianke) Biotech Co Ltd)


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    Multi Sciences (Lianke) Biotech Co Ltd permeabilization buffer set
    Permeabilization Buffer Set, supplied by Multi Sciences (Lianke) Biotech Co Ltd, used in various techniques. Bioz Stars score: 96/100, based on 107 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/permeabilization+buffer+set/Flow+Cytometry+Staining+buffer/pm41864339-53-6-10
    Average 96 stars, based on 107 article reviews
    permeabilization buffer set - by Bioz Stars, 2026-09
    96/100 stars

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    Related Articles

    Staining:

    Article Title: Cyclovirobuxine D suppresses cancer stemness in osteosarcoma with implication of the noncanonical NF-kappaB pathway
    Article Snippet: Before processing, wash with PBS, then wash with Staining buffer (Multisciences (Lianke) Biotech, China), and discard the supernatant while avoiding light. .. Resuspend in PI/RNase staining buffer (Multisciences (Lianke) Biotech, China), avoiding light, and incubate for 5–10 min before analysis. ..

    Article Title: Regulatory mechanisms of ALKBH5/CIITA axis in the synergistic modulation of hepatocellular carcinoma radiotherapy and immunotherapy.
    Article Snippet: .. They were then resuspended in 1 milliliter of DNA Staining Solution (sourced from Hangzhou Lianke Biotechnology Co., Ltd., China) and incubated for 30min in an environment devoid of light. .. The final stage entailed the assessment of the cell-cycle distribution of the treated cells, employing a Beckman Coulter flow cytometer for this purpose.

    Article Title: Circ-find-0001774 Modulates Parkinson's Disease via miR-153-3p: Mechanistic Insights and Therapeutic Implications.
    Article Snippet: 1 Department of Neurosurgery, Jiangxi Provincial People’s Hospital, The First Affiliated Hospital of Nanchang Medical College, No.266, Fenghe North Avenue, Honggutan District, Nanchang 330038, Jiangxi, PR China 2 Department of Neurosurgery, Xiangya Hospital, Central South University, Jiangxi (National Regional Medical Center for Neurological Diseases), Nanchang, China 3 Department of Neurology, Xiangya Hospital, Central South University, Jiangxi(National Regional Medical Center for Neurological Diseases), Nanchang, China 4 Department of Neurology, Jiangxi Provincial People’s Hospital, The First Affiliated Hospital of Nanchang Medical College, No.266, Fenghe North Avenue, Honggutan District, Nanchang, Jiangxi 330038, PR China 5 Jiangxi Medical College, Nanchang University, Nanchang, China Abstract Objective This study aimed to investigate how circ-find-0001774 regulates miR-153-3p in Parkinson’s disease (PD).. Methods We first validated the targeting relationship between circ-find-0001774 and miR-153-3p using dual-luciferase reporter assays, excluding any association with let-7a-5p.. Next, we constructed a circ-find-0001774 overexpression vector and transfected it into MN9D dopaminergic neurons, confirming transfection efficiency by qPCR.

    Article Title: R-propranolol Promotes the Adipogenesis and Subsequent Apoptosis of Hemangioma Stem Cells through the PERK Signaling Pathway.
    Article Snippet: From the State Key Laboratory of Oral and Maxillofacial Reconstruction and Regeneration,* Key Laboratory of Oral Biomedicine Ministry of Education, Hubei Key Laboratory of Stomatology, and the Departments of Oral and Maxillofacial Surgery and Pathology, School and Hospital of Stomatology, Wuhan University, Wuhan; the Department of Stomatology, The Central Hospital of Enshi Tujia and Miao Autonomous Prefecture, Enshi; the Department of Plastic Surgery, Wuhan Children’s Hospital, Wuhan; and the Wuhan Conform Pharm Co, Ltd, Wuhan, China

    Article Title: Circ-find-0001774 Modulates Parkinson’s Disease via miR-153-3p: Mechanistic Insights and Therapeutic Implications
    Article Snippet: .. The cells were resuspended in 300 μL of pre-cooled 1× Binding Buffer and stained with 5 μL of Annexin V-FITC and 10 μL of PI (MULTI SCIENCES, AP101-100-kit). .. After gentle mixing, the cells were incubated in the dark at room temperature for 10 min and then analyzed using a flow cytometer (NovoCyte 2060R, Acea Biosciences).

    Article Title: Cyclovirobuxine D suppresses cancer stemness in osteosarcoma with implication of the noncanonical NF-kappaB pathway
    Article Snippet: .. Before processing, wash with PBS, then wash with Staining buffer (Multisciences (Lianke) Biotech, China), and discard the supernatant while avoiding light. .. Resuspend in PI/RNase staining buffer (Multisciences (Lianke) Biotech, China), avoiding light, and incubate for 5–10 min before analysis.

    Article Title: Cyclovirobuxine D suppresses cancer stemness in osteosarcoma with implication of the noncanonical NF-kappaB pathway
    Article Snippet: Before processing, wash with PBS, then wash with Staining buffer (Multisciences (Lianke) Biotech, China), and discard the supernatant while avoiding light. .. Resuspend in PI/RNase staining buffer (Multisciences (Lianke) Biotech, China), avoiding light, and incubate for 5–10 min before analysis. ..

    Article Title: Integrated Single-Cell Profiling Reveals TL1A as a Biomarker and Driver of Type 2 Inflammation via Macrophage-Dependent Immunoregulation in Asthma
    Article Snippet: To label intercellular proteins, including S100A4 (Abcam), forkhead box protein P3 (Foxp3; MultiSciences), IL-4 (MultiSciences), and interleukin 17A (IL-17A, MultiSciences), cells were first fixed with intracellular fixation and permeabilization buffer A (MultiSciences) for 15 min. After washing, the cells were resuspended and incubated on ice with the corresponding flow cytometric antibodies (anti-S100A4, anti-Foxp3, anti-IL-4, and anti-IL-17A) and permeabilization buffer B (MultiSciences) for 30 min at 4 °C. .. The cells were subsequently washed with Flow Cytometry Staining Buffer (MultiSciences) and collected after centrifugation at 3,000 rpm for 5 min at 4 °C. .. Finally, the cells were analyzed using a FACSCalibur or FACSAria III (BD Biosciences) flow cytometer and the FlowJo 10.8.1 software.

    Incubation:

    Article Title: Regulatory mechanisms of ALKBH5/CIITA axis in the synergistic modulation of hepatocellular carcinoma radiotherapy and immunotherapy.
    Article Snippet: .. They were then resuspended in 1 milliliter of DNA Staining Solution (sourced from Hangzhou Lianke Biotechnology Co., Ltd., China) and incubated for 30min in an environment devoid of light. .. The final stage entailed the assessment of the cell-cycle distribution of the treated cells, employing a Beckman Coulter flow cytometer for this purpose.

    Binding Assay:

    Article Title: Circ-find-0001774 Modulates Parkinson's Disease via miR-153-3p: Mechanistic Insights and Therapeutic Implications.
    Article Snippet: 1 Department of Neurosurgery, Jiangxi Provincial People’s Hospital, The First Affiliated Hospital of Nanchang Medical College, No.266, Fenghe North Avenue, Honggutan District, Nanchang 330038, Jiangxi, PR China 2 Department of Neurosurgery, Xiangya Hospital, Central South University, Jiangxi (National Regional Medical Center for Neurological Diseases), Nanchang, China 3 Department of Neurology, Xiangya Hospital, Central South University, Jiangxi(National Regional Medical Center for Neurological Diseases), Nanchang, China 4 Department of Neurology, Jiangxi Provincial People’s Hospital, The First Affiliated Hospital of Nanchang Medical College, No.266, Fenghe North Avenue, Honggutan District, Nanchang, Jiangxi 330038, PR China 5 Jiangxi Medical College, Nanchang University, Nanchang, China Abstract Objective This study aimed to investigate how circ-find-0001774 regulates miR-153-3p in Parkinson’s disease (PD).. Methods We first validated the targeting relationship between circ-find-0001774 and miR-153-3p using dual-luciferase reporter assays, excluding any association with let-7a-5p.. Next, we constructed a circ-find-0001774 overexpression vector and transfected it into MN9D dopaminergic neurons, confirming transfection efficiency by qPCR.

    Article Title: Circ-find-0001774 Modulates Parkinson’s Disease via miR-153-3p: Mechanistic Insights and Therapeutic Implications
    Article Snippet: .. The cells were resuspended in 300 μL of pre-cooled 1× Binding Buffer and stained with 5 μL of Annexin V-FITC and 10 μL of PI (MULTI SCIENCES, AP101-100-kit). .. After gentle mixing, the cells were incubated in the dark at room temperature for 10 min and then analyzed using a flow cytometer (NovoCyte 2060R, Acea Biosciences).

    Flow Cytometry:

    Article Title: Integrated Single-Cell Profiling Reveals TL1A as a Biomarker and Driver of Type 2 Inflammation via Macrophage-Dependent Immunoregulation in Asthma
    Article Snippet: To label intercellular proteins, including S100A4 (Abcam), forkhead box protein P3 (Foxp3; MultiSciences), IL-4 (MultiSciences), and interleukin 17A (IL-17A, MultiSciences), cells were first fixed with intracellular fixation and permeabilization buffer A (MultiSciences) for 15 min. After washing, the cells were resuspended and incubated on ice with the corresponding flow cytometric antibodies (anti-S100A4, anti-Foxp3, anti-IL-4, and anti-IL-17A) and permeabilization buffer B (MultiSciences) for 30 min at 4 °C. .. The cells were subsequently washed with Flow Cytometry Staining Buffer (MultiSciences) and collected after centrifugation at 3,000 rpm for 5 min at 4 °C. .. Finally, the cells were analyzed using a FACSCalibur or FACSAria III (BD Biosciences) flow cytometer and the FlowJo 10.8.1 software.

    Centrifugation:

    Article Title: Integrated Single-Cell Profiling Reveals TL1A as a Biomarker and Driver of Type 2 Inflammation via Macrophage-Dependent Immunoregulation in Asthma
    Article Snippet: To label intercellular proteins, including S100A4 (Abcam), forkhead box protein P3 (Foxp3; MultiSciences), IL-4 (MultiSciences), and interleukin 17A (IL-17A, MultiSciences), cells were first fixed with intracellular fixation and permeabilization buffer A (MultiSciences) for 15 min. After washing, the cells were resuspended and incubated on ice with the corresponding flow cytometric antibodies (anti-S100A4, anti-Foxp3, anti-IL-4, and anti-IL-17A) and permeabilization buffer B (MultiSciences) for 30 min at 4 °C. .. The cells were subsequently washed with Flow Cytometry Staining Buffer (MultiSciences) and collected after centrifugation at 3,000 rpm for 5 min at 4 °C. .. Finally, the cells were analyzed using a FACSCalibur or FACSAria III (BD Biosciences) flow cytometer and the FlowJo 10.8.1 software.



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    Image Search Results


    Schematic workflow and bioinformatics analysis of the ST-FFPE-mIF whole solution. (1) FFPE tissue section was mounted on the chip and performed de-paraffinization (2) The section on the chip was subjected to antigen repair, blocking, antibody incubation, and mIF imaging. Before the 2nd round of mIF staining, antibodies from the 1 st round should be removal, and the epitope would be re-exposed. Then, the above mIF protocol should be repeated to generate another mIF image. Nine-colored mIF images were obtained accordingly (3) Permeabilization, in situ cDNA synthesis and collection were conducted after De-crosslink (4) cDNA amplification, library construction, and sequencing were performed according to manufacturer’s protocol to obtain Stereo-seq sequencing result (5) mIF images and spatially resolved gene expression was subjected to downstream spatial visualization and bioinformatics analyses including image processing and spatial multi-omics analysis to address scientific questions

    Journal: Genome Biology

    Article Title: ST-FFPE-mIF: integrating spatial transcriptomics and multiplex immunofluorescence in formalin-fixed paraffin-embedded tissues using Stereo-seq

    doi: 10.1186/s13059-025-03900-3

    Figure Lengend Snippet: Schematic workflow and bioinformatics analysis of the ST-FFPE-mIF whole solution. (1) FFPE tissue section was mounted on the chip and performed de-paraffinization (2) The section on the chip was subjected to antigen repair, blocking, antibody incubation, and mIF imaging. Before the 2nd round of mIF staining, antibodies from the 1 st round should be removal, and the epitope would be re-exposed. Then, the above mIF protocol should be repeated to generate another mIF image. Nine-colored mIF images were obtained accordingly (3) Permeabilization, in situ cDNA synthesis and collection were conducted after De-crosslink (4) cDNA amplification, library construction, and sequencing were performed according to manufacturer’s protocol to obtain Stereo-seq sequencing result (5) mIF images and spatially resolved gene expression was subjected to downstream spatial visualization and bioinformatics analyses including image processing and spatial multi-omics analysis to address scientific questions

    Article Snippet: Post-fixation, the Stereo-seq chip was air-dried, and the tissue section was incubated in permeabilization buffer (Cat# 211SN114, STOmics) supplemented with 3 μL of Tetramethylene sulfone (Cat#A610163, Sangon Biotech) for 25 min at 37 °C.

    Techniques: Blocking Assay, Incubation, Imaging, Staining, In Situ, cDNA Synthesis, Amplification, Sequencing, Gene Expression, Biomarker Discovery