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trsa sequence  (Addgene inc)


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    Structured Review

    Addgene inc trsa sequence
    Figure 5. sarID <t>identifies</t> <t>NEAT1-interacting</t> transcripts in living cells. a) Read coverage at the AGO2 locus. C-to-U editing was indicated by the color. Brown and green indicate the abundances of C and U sites, respectively. b) Violin plot of C-to-U editing rates in the control and NEAT1 groups. n = 390 and 2341 for control and NEAT1 respectively; Wilcoxon test. c) Overlap of sites and genes identified in the control and NEAT1 groups. d) Metagene density plot of the distribution of C-to-U editing sites. e) Pathway enrichment analysis of interacting transcripts of NEAT1. f) Scheme of the <t>tRSA-tagged</t>
    Trsa Sequence, supplied by Addgene inc, used in various techniques. Bioz Stars score: 93/100, based on 7 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/trsa sequence/product/Addgene inc
    Average 93 stars, based on 7 article reviews
    trsa sequence - by Bioz Stars, 2026-02
    93/100 stars

    Images

    1) Product Images from "CRISPR/Cas13 sgRNA-Mediated RNA-RNA Interaction Mapping in Live Cells with APOBEC RNA Editing."

    Article Title: CRISPR/Cas13 sgRNA-Mediated RNA-RNA Interaction Mapping in Live Cells with APOBEC RNA Editing.

    Journal: Advanced science (Weinheim, Baden-Wurttemberg, Germany)

    doi: 10.1002/advs.202409004

    Figure 5. sarID identifies NEAT1-interacting transcripts in living cells. a) Read coverage at the AGO2 locus. C-to-U editing was indicated by the color. Brown and green indicate the abundances of C and U sites, respectively. b) Violin plot of C-to-U editing rates in the control and NEAT1 groups. n = 390 and 2341 for control and NEAT1 respectively; Wilcoxon test. c) Overlap of sites and genes identified in the control and NEAT1 groups. d) Metagene density plot of the distribution of C-to-U editing sites. e) Pathway enrichment analysis of interacting transcripts of NEAT1. f) Scheme of the tRSA-tagged
    Figure Legend Snippet: Figure 5. sarID identifies NEAT1-interacting transcripts in living cells. a) Read coverage at the AGO2 locus. C-to-U editing was indicated by the color. Brown and green indicate the abundances of C and U sites, respectively. b) Violin plot of C-to-U editing rates in the control and NEAT1 groups. n = 390 and 2341 for control and NEAT1 respectively; Wilcoxon test. c) Overlap of sites and genes identified in the control and NEAT1 groups. d) Metagene density plot of the distribution of C-to-U editing sites. e) Pathway enrichment analysis of interacting transcripts of NEAT1. f) Scheme of the tRSA-tagged

    Techniques Used: Control



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    Figure 5. sarID <t>identifies</t> <t>NEAT1-interacting</t> transcripts in living cells. a) Read coverage at the AGO2 locus. C-to-U editing was indicated by the color. Brown and green indicate the abundances of C and U sites, respectively. b) Violin plot of C-to-U editing rates in the control and NEAT1 groups. n = 390 and 2341 for control and NEAT1 respectively; Wilcoxon test. c) Overlap of sites and genes identified in the control and NEAT1 groups. d) Metagene density plot of the distribution of C-to-U editing sites. e) Pathway enrichment analysis of interacting transcripts of NEAT1. f) Scheme of the <t>tRSA-tagged</t>
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    Figure 5. sarID <t>identifies</t> <t>NEAT1-interacting</t> transcripts in living cells. a) Read coverage at the AGO2 locus. C-to-U editing was indicated by the color. Brown and green indicate the abundances of C and U sites, respectively. b) Violin plot of C-to-U editing rates in the control and NEAT1 groups. n = 390 and 2341 for control and NEAT1 respectively; Wilcoxon test. c) Overlap of sites and genes identified in the control and NEAT1 groups. d) Metagene density plot of the distribution of C-to-U editing sites. e) Pathway enrichment analysis of interacting transcripts of NEAT1. f) Scheme of the <t>tRSA-tagged</t>
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    Image Search Results


    Figure 5. sarID identifies NEAT1-interacting transcripts in living cells. a) Read coverage at the AGO2 locus. C-to-U editing was indicated by the color. Brown and green indicate the abundances of C and U sites, respectively. b) Violin plot of C-to-U editing rates in the control and NEAT1 groups. n = 390 and 2341 for control and NEAT1 respectively; Wilcoxon test. c) Overlap of sites and genes identified in the control and NEAT1 groups. d) Metagene density plot of the distribution of C-to-U editing sites. e) Pathway enrichment analysis of interacting transcripts of NEAT1. f) Scheme of the tRSA-tagged

    Journal: Advanced science (Weinheim, Baden-Wurttemberg, Germany)

    Article Title: CRISPR/Cas13 sgRNA-Mediated RNA-RNA Interaction Mapping in Live Cells with APOBEC RNA Editing.

    doi: 10.1002/advs.202409004

    Figure Lengend Snippet: Figure 5. sarID identifies NEAT1-interacting transcripts in living cells. a) Read coverage at the AGO2 locus. C-to-U editing was indicated by the color. Brown and green indicate the abundances of C and U sites, respectively. b) Violin plot of C-to-U editing rates in the control and NEAT1 groups. n = 390 and 2341 for control and NEAT1 respectively; Wilcoxon test. c) Overlap of sites and genes identified in the control and NEAT1 groups. d) Metagene density plot of the distribution of C-to-U editing sites. e) Pathway enrichment analysis of interacting transcripts of NEAT1. f) Scheme of the tRSA-tagged

    Article Snippet: For overexpressing tRSA tagged NEAT1, the tRSA sequence amplified from pcDNA3-tRSA (Addgene# 32200) was subcloned between the XbaI and NotI sites into the pCDH-puro vector.

    Techniques: Control