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permeabilization buffer  (Complete Genomics Inc)


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    Structured Review

    Complete Genomics Inc permeabilization buffer
    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) <t>Permeabilization,</t> 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
    Permeabilization Buffer, supplied by Complete Genomics Inc, used in various techniques. Bioz Stars score: 99/100, based on 495 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/permeabilization+buffer+set/Stereo-seq+Transcriptomics+Set+for+FFPE/pmc12709731-202-13-17
    Average 99 stars, based on 495 article reviews
    permeabilization buffer - by Bioz Stars, 2026-11
    99/100 stars

    Images

    1) Product Images from "ST-FFPE-mIF: integrating spatial transcriptomics and multiplex immunofluorescence in formalin-fixed paraffin-embedded tissues using Stereo-seq"

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

    Journal: Genome Biology

    doi: 10.1186/s13059-025-03900-3

    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
    Figure Legend 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

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

    Related Articles

    Incubation:

    Article Title: Stereo-seq of the prefrontal cortex in aging and Alzheimer’s disease
    Article Snippet: The nuclei images were captured using a Zeiss Axio Scan Z1 microscope (at EGFP wavelength). .. Subsequently, the tissue section was incubated in the permeabilization buffer (Cat # 111KP118, STOmics America Ltd) for 12 mins at 37 °C. ..

    Article Title: ST-FFPE-mIF: integrating spatial transcriptomics and multiplex immunofluorescence in formalin-fixed paraffin-embedded tissues using Stereo-seq
    Article Snippet: Fixation in pre-cooled methanol (Cat# 34860, Sigma) for 30 min at − 20 °C ensued. .. 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. .. After permeabilization, the FFPE Dimer mix (Cat#211SN114, STOmics) was added and incubated at room temperature for 40 min.

    Article Title: Stereo-seq of the prefrontal cortex in aging and Alzheimer's disease.
    Article Snippet: .. Subsequently, the tissue section was incubated in the permeabilization buffer (Cat # 111KP118, STOmics America Ltd) for 12mins at 37 °C. ..

    Article Title: ST-FFPE-mIF: Integrating Spatial Transcriptomics and Multiplex Immunofluorescence in Formalin-Fixed Paraffin-Embedded Tissues Using Stereo-seq
    Article Snippet: Fixation in pre-cooled methanol (Cat# 34860, Sigma) for 30 min at −20°C ensued. .. 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. .. After permeabilization, the FFPE Dimer mix (Cat#211SN114, STOmics) was added and incubated at room temperature for 40 min.

    Article Title: ST-FFPE-mIF: integrating spatial transcriptomics and multiplex immunofluorescence in formalin-fixed paraffin-embedded tissues using Stereo-seq.
    Article Snippet: Fixation in pre-cooled methanol (Cat# 34860, Sigma) for 30 min at − 20 °C ensued. .. 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. .. After permeabilization, the FFPE Dimer mix (Cat#211SN114, STOmics) was added and incubated at room temperature for 40 min.

    other:

    Article Title: Psychedelic control of neuroimmune interactions governing fear.
    Article Snippet: Elizabeth N. Chung, Jinsu Lee, Carolina M. Polonio, Joshua Choi, Camilo Faust Akl, Michael Kilian, Wiebke M. Weiß, Georgia Gunner, Mingyu Ye, Tae Hyun Heo, Sienna S. Drake, Liu Yang, Catarina R. G. L. d’Eca, Joon-Hyuk Lee, Liwen Deng, Daniel Farrenkopf, Anton M. Schüle, Hong-Gyun Lee, Oreoluwa Afolabi, Sharmin Ghaznavi, Stelios M. Smirnakis, Isaac M. Chiu, Vijay K. Kuchroo, Francisco J. Quintana & Michael A. Wheeler1,2 ✉

    Article Title: Morphogenic, molecular and cellular adaptations for unidirectional airflow in the chicken lung.
    Article Snippet: Briefly, the tissue section on the Stereo-seq chip (1 cm×1 cm) was incubated at 37°C for 5 min and subsequently fixed in pre-cooled methanol (34860, Sigma-Aldrich; precooled for 30 mins at −20°C) at −20°C.

    Transcriptomics:

    Article Title: Quasi-spatial single-cell transcriptome based on physical tissue properties defines early aging associated niche in liver.
    Article Snippet: Aging is associated with the accumulation of senescent cells, which are triggered by tissue injury response and often escape clearance by the immune system.. The specific traits and diversity of these cells in aged tissues, along with their effects on the t is sue m ic ro en vi ro nment, remain largely unexplored.. Despite the advances in single-cell and spatial omics technologies to understand complex tissue architecture, senescent cell populations are often neglected in general analysis pipelines due to their scarcity and the technical bias in current omics toolkits.



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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