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targeting vector  (New England Biolabs)


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    Structured Review

    New England Biolabs targeting vector
    Targeting Vector, supplied by New England Biolabs, used in various techniques. Bioz Stars score: 96/100, based on 1386 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/targeting vector/product/New England Biolabs
    Average 96 stars, based on 1386 article reviews
    targeting vector - by Bioz Stars, 2026-06
    96/100 stars

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    Inhibition of <t>circFRRS1</t> alleviates the inflammation damage of PC-12 cells after H-OGD/R treatment. (A) Sequence diagram of circFRRS1. (B) The inhibition effects of si-circFRRS1 were detected by RT-PCR. (C) CCK8 assay revealed circFRRS1 inhibition improved the survival rate of H-OGD/R treated PC-12 cells. (D–F) The inhibition of circFRRS1 reduced the increasing level of TNF-α, IL-6, and IL-1β induced by H-OGD/R treatment. (G) The inhibition of circFRRS1 alleviated the NLRP3 inflammasome activation of H-OGD/R treated PC-12 cells. *** p < 0.001, vs. si-NC group; ## p < 0.01, ### p < 0.001, vs. H-OGD/R + si-NC group.
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    Inhibition of circFRRS1 alleviates the inflammation damage of PC-12 cells after H-OGD/R treatment. (A) Sequence diagram of circFRRS1. (B) The inhibition effects of si-circFRRS1 were detected by RT-PCR. (C) CCK8 assay revealed circFRRS1 inhibition improved the survival rate of H-OGD/R treated PC-12 cells. (D–F) The inhibition of circFRRS1 reduced the increasing level of TNF-α, IL-6, and IL-1β induced by H-OGD/R treatment. (G) The inhibition of circFRRS1 alleviated the NLRP3 inflammasome activation of H-OGD/R treated PC-12 cells. *** p < 0.001, vs. si-NC group; ## p < 0.01, ### p < 0.001, vs. H-OGD/R + si-NC group.

    Journal: Frontiers in Cellular Neuroscience

    Article Title: CircFRRS1 drives neuroinflammation through the miR-27a-3p/TLR4 pathway after deep hypothermic circulatory arrest

    doi: 10.3389/fncel.2026.1750887

    Figure Lengend Snippet: Inhibition of circFRRS1 alleviates the inflammation damage of PC-12 cells after H-OGD/R treatment. (A) Sequence diagram of circFRRS1. (B) The inhibition effects of si-circFRRS1 were detected by RT-PCR. (C) CCK8 assay revealed circFRRS1 inhibition improved the survival rate of H-OGD/R treated PC-12 cells. (D–F) The inhibition of circFRRS1 reduced the increasing level of TNF-α, IL-6, and IL-1β induced by H-OGD/R treatment. (G) The inhibition of circFRRS1 alleviated the NLRP3 inflammasome activation of H-OGD/R treated PC-12 cells. *** p < 0.001, vs. si-NC group; ## p < 0.01, ### p < 0.001, vs. H-OGD/R + si-NC group.

    Article Snippet: The shRNA lentiviral vectors targeting circFRRS1 (sh-circFRRS1) and the negative control (sh-NC) were obtained from Genechem (Shanghai, China).

    Techniques: Inhibition, Sequencing, Reverse Transcription Polymerase Chain Reaction, CCK-8 Assay, Activation Assay

    Dual luciferase reporter experiment confirmed the regulatory relationships of circFRRS1/rno-miR-27a-3p and rno-miR-27a-3p/TLR4 pairs. (A) The predicting binding site between circFRRS1 and miR-27a-3p. (B) Dual luciferase reporter assay revealed that miR-27a-3p attenuated the luciferase activity of circFRRS1-WT, but not of circFRRS1-MUT. (C) The predicting binding site between TLR4 and miR-27a-3p. (D) Dual luciferase reporter assay revealed that miR-27a-3p attenuated the luciferase activity of TLR4 3’-WT, but not of TLR4 3’-MUT. ** p < 0.01, *** p < 0.001, vs. control group; # p < 0.05, ### p < 0.001, vs. WT group.

    Journal: Frontiers in Cellular Neuroscience

    Article Title: CircFRRS1 drives neuroinflammation through the miR-27a-3p/TLR4 pathway after deep hypothermic circulatory arrest

    doi: 10.3389/fncel.2026.1750887

    Figure Lengend Snippet: Dual luciferase reporter experiment confirmed the regulatory relationships of circFRRS1/rno-miR-27a-3p and rno-miR-27a-3p/TLR4 pairs. (A) The predicting binding site between circFRRS1 and miR-27a-3p. (B) Dual luciferase reporter assay revealed that miR-27a-3p attenuated the luciferase activity of circFRRS1-WT, but not of circFRRS1-MUT. (C) The predicting binding site between TLR4 and miR-27a-3p. (D) Dual luciferase reporter assay revealed that miR-27a-3p attenuated the luciferase activity of TLR4 3’-WT, but not of TLR4 3’-MUT. ** p < 0.01, *** p < 0.001, vs. control group; # p < 0.05, ### p < 0.001, vs. WT group.

    Article Snippet: The shRNA lentiviral vectors targeting circFRRS1 (sh-circFRRS1) and the negative control (sh-NC) were obtained from Genechem (Shanghai, China).

    Techniques: Luciferase, Binding Assay, Reporter Assay, Activity Assay, Control

    The inhibition of circFRRS1 suppressed TLR4/NF-κB/NLRP3 pathway in H-OGD/R-induced PC-12 cells. (A) WB analysis revealed that the TLR4/NF-κB/NLRP3 axis was activated in H-OGD/R-induced PC-12 cells and markedly inhibited after si-circFRRS1 transfected. (B–G) Statistical analysis of WB results. * p < 0.05; ** p < 0.01, *** p < 0.001, vs. si-NC group; # p < 0.05, ## p < 0.01, vs. H-OGD/R + si-NC group.

    Journal: Frontiers in Cellular Neuroscience

    Article Title: CircFRRS1 drives neuroinflammation through the miR-27a-3p/TLR4 pathway after deep hypothermic circulatory arrest

    doi: 10.3389/fncel.2026.1750887

    Figure Lengend Snippet: The inhibition of circFRRS1 suppressed TLR4/NF-κB/NLRP3 pathway in H-OGD/R-induced PC-12 cells. (A) WB analysis revealed that the TLR4/NF-κB/NLRP3 axis was activated in H-OGD/R-induced PC-12 cells and markedly inhibited after si-circFRRS1 transfected. (B–G) Statistical analysis of WB results. * p < 0.05; ** p < 0.01, *** p < 0.001, vs. si-NC group; # p < 0.05, ## p < 0.01, vs. H-OGD/R + si-NC group.

    Article Snippet: The shRNA lentiviral vectors targeting circFRRS1 (sh-circFRRS1) and the negative control (sh-NC) were obtained from Genechem (Shanghai, China).

    Techniques: Inhibition, Transfection

    circFRRS1 can regulate TLR4 by targeting miR-27a-3p. (A) Administration of miR-27a-3p inhibitor could reverse the downregulation of TLR4 expression by transfecting si-circFRRS1. (B) Further protein-level detection using WB gave the further validation. *** p < 0.001, vs. si-NC group; # p < 0.05, ## p < 0.01, ### p < 0.001, vs. H-OGD/R + si-NC group or H-OGD/R + si-circ group.

    Journal: Frontiers in Cellular Neuroscience

    Article Title: CircFRRS1 drives neuroinflammation through the miR-27a-3p/TLR4 pathway after deep hypothermic circulatory arrest

    doi: 10.3389/fncel.2026.1750887

    Figure Lengend Snippet: circFRRS1 can regulate TLR4 by targeting miR-27a-3p. (A) Administration of miR-27a-3p inhibitor could reverse the downregulation of TLR4 expression by transfecting si-circFRRS1. (B) Further protein-level detection using WB gave the further validation. *** p < 0.001, vs. si-NC group; # p < 0.05, ## p < 0.01, ### p < 0.001, vs. H-OGD/R + si-NC group or H-OGD/R + si-circ group.

    Article Snippet: The shRNA lentiviral vectors targeting circFRRS1 (sh-circFRRS1) and the negative control (sh-NC) were obtained from Genechem (Shanghai, China).

    Techniques: Expressing, Biomarker Discovery