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stereo-seq transcriptomics set for chip-on-a-slide  (Complete Genomics Inc)


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    Complete Genomics Inc stereo-seq transcriptomics set for chip-on-a-slide
    Stereo Seq Transcriptomics Set For Chip On A Slide, supplied by Complete Genomics Inc, used in various techniques. Bioz Stars score: 99/100, based on 116 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/slide+seq/Stereo-seq+Transcriptomics+Set+for+Chip-on-a-slide/custom%40211st114%4042413505
    Average 99 stars, based on 116 article reviews
    stereo-seq transcriptomics set for chip-on-a-slide - by Bioz Stars, 2026-09
    99/100 stars

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    Related Articles

    Spatial & Multi-Omics:

    Article Title: Mapping brain-wide monosynaptic inputs to single neurons with ROInet-seq.
    Article Snippet: thesia on the harvest day. Brains were snap frozen on dry ice and stored at -80◦C until sectioning the following day. Tissue mounting was performed according to the steps outlined by the manufactorer (STOmics, Stereo-seq transcriptomics set for chip-on-a-slide V1.2, manual version A1). The tissue was sectioned into 10μm-thick slices, and the target region (hippocampus) was trimmed with a blade and

    Single-Cell Sequencing:

    Article Title: Mapping brain-wide monosynaptic inputs to single neurons with ROInet-seq.
    Article Snippet: thesia on the harvest day. Brains were snap frozen on dry ice and stored at -80◦C until sectioning the following day. Tissue mounting was performed according to the steps outlined by the manufactorer (STOmics, Stereo-seq transcriptomics set for chip-on-a-slide V1.2, manual version A1). The tissue was sectioned into 10μm-thick slices, and the target region (hippocampus) was trimmed with a blade and

    Targeted Sequencing:

    Article Title: Mapping brain-wide monosynaptic inputs to single neurons with ROInet-seq.
    Article Snippet: thesia on the harvest day. Brains were snap frozen on dry ice and stored at -80◦C until sectioning the following day. Tissue mounting was performed according to the steps outlined by the manufactorer (STOmics, Stereo-seq transcriptomics set for chip-on-a-slide V1.2, manual version A1). The tissue was sectioned into 10μm-thick slices, and the target region (hippocampus) was trimmed with a blade and

    Whole-Exome Sequencing:

    Article Title: Mapping brain-wide monosynaptic inputs to single neurons with ROInet-seq.
    Article Snippet: thesia on the harvest day. Brains were snap frozen on dry ice and stored at -80◦C until sectioning the following day. Tissue mounting was performed according to the steps outlined by the manufactorer (STOmics, Stereo-seq transcriptomics set for chip-on-a-slide V1.2, manual version A1). The tissue was sectioned into 10μm-thick slices, and the target region (hippocampus) was trimmed with a blade and

    Metagenomics & Microbiome:

    Article Title: Mapping brain-wide monosynaptic inputs to single neurons with ROInet-seq.
    Article Snippet: thesia on the harvest day. Brains were snap frozen on dry ice and stored at -80◦C until sectioning the following day. Tissue mounting was performed according to the steps outlined by the manufactorer (STOmics, Stereo-seq transcriptomics set for chip-on-a-slide V1.2, manual version A1). The tissue was sectioned into 10μm-thick slices, and the target region (hippocampus) was trimmed with a blade and

    Bulk RNA Sequencing:

    Article Title: Mapping brain-wide monosynaptic inputs to single neurons with ROInet-seq.
    Article Snippet: thesia on the harvest day. Brains were snap frozen on dry ice and stored at -80◦C until sectioning the following day. Tissue mounting was performed according to the steps outlined by the manufactorer (STOmics, Stereo-seq transcriptomics set for chip-on-a-slide V1.2, manual version A1). The tissue was sectioned into 10μm-thick slices, and the target region (hippocampus) was trimmed with a blade and

    Epigenomics & Chromatin Profiling:

    Article Title: Mapping brain-wide monosynaptic inputs to single neurons with ROInet-seq.
    Article Snippet: thesia on the harvest day. Brains were snap frozen on dry ice and stored at -80◦C until sectioning the following day. Tissue mounting was performed according to the steps outlined by the manufactorer (STOmics, Stereo-seq transcriptomics set for chip-on-a-slide V1.2, manual version A1). The tissue was sectioned into 10μm-thick slices, and the target region (hippocampus) was trimmed with a blade and



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    AIR-SPACE enables the mapping of adaptive immune receptor (AIR) clonotypes and <t>transcriptomics</t> in situ. ( A ) Schematic of the experimental design and methodology, including the generation of long-read (LR) and short-read (SR). ( B ) Spatial mapping of cell types across the LN sections at different time points postinfection. (Scale bar, 500 μm.) ( C ) Spatial mapping of AIR clonotypes across the LN sections, with immunoglobulin (IG) clones shown in blue and T cell receptor (TCR) clones shown in red; outlined with germinal center (GC) regions in LNs from D10PI to D21PI. ( D ) Multiplexed RNA FISH staining for T cell marker Trbc2 (green), B cell marker Ms4a1 (red), and DAPI (blue) across all samples on sister sections. (Scale bar 500 μm.)
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    Image Search Results


    AIR-SPACE enables the mapping of adaptive immune receptor (AIR) clonotypes and transcriptomics in situ. ( A ) Schematic of the experimental design and methodology, including the generation of long-read (LR) and short-read (SR). ( B ) Spatial mapping of cell types across the LN sections at different time points postinfection. (Scale bar, 500 μm.) ( C ) Spatial mapping of AIR clonotypes across the LN sections, with immunoglobulin (IG) clones shown in blue and T cell receptor (TCR) clones shown in red; outlined with germinal center (GC) regions in LNs from D10PI to D21PI. ( D ) Multiplexed RNA FISH staining for T cell marker Trbc2 (green), B cell marker Ms4a1 (red), and DAPI (blue) across all samples on sister sections. (Scale bar 500 μm.)

    Journal: Proceedings of the National Academy of Sciences of the United States of America

    Article Title: A temporal and spatial atlas of adaptive immune responses in the lymph node following viral infection

    doi: 10.1073/pnas.2504742123

    Figure Lengend Snippet: AIR-SPACE enables the mapping of adaptive immune receptor (AIR) clonotypes and transcriptomics in situ. ( A ) Schematic of the experimental design and methodology, including the generation of long-read (LR) and short-read (SR). ( B ) Spatial mapping of cell types across the LN sections at different time points postinfection. (Scale bar, 500 μm.) ( C ) Spatial mapping of AIR clonotypes across the LN sections, with immunoglobulin (IG) clones shown in blue and T cell receptor (TCR) clones shown in red; outlined with germinal center (GC) regions in LNs from D10PI to D21PI. ( D ) Multiplexed RNA FISH staining for T cell marker Trbc2 (green), B cell marker Ms4a1 (red), and DAPI (blue) across all samples on sister sections. (Scale bar 500 μm.)

    Article Snippet: Slide-seq spatial transcriptomics experiment was performed using the Curio Seeker Kit (Curio Bioscience) according to manufacturer instructions.

    Techniques: In Situ, Clone Assay, Staining, Marker