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pt2 shp53 plasmid  (Addgene inc)


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    Structured Review

    Addgene inc pt2 shp53 plasmid
    Pt2 Shp53 Plasmid, 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
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    Average 93 stars, based on 7 article reviews
    pt2 shp53 plasmid - by Bioz Stars, 2026-06
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    siCtnnb1 and siAnln decreased tumor burden in the NRAS G12V / <t>shp53</t> HCC model. (A) Schematic of NRAS G12V / shp53 mouse model receiving continuous siRNA injections. Male C57BL/6J mice underwent HDT injection at 8 weeks of age, i.e. start timepoint of 0 weeks (0w). Injections of siRNA (5 mg/kg) started 4 days later (0.5w) and continued every other week (2.5w, 4.5w, 6.5w). Mice were sacrificed 1 week after the fourth siRNA dose (7.5w). (B) Schematic of NRAS G12V / shp53 mouse model receiving transient siRNA injections. Male C57BL/6J mice underwent HDT injection at 8 weeks of age (0w). Injections of siRNA (5 mg/kg) started 4 days later and continued every other week for a total of two doses (0.5w and 2.5w). Mice were sacrificed 5 weeks after the second siRNA dose (7.5w). (C) Liver-to-body-weight ratios for NRAS G12V / shp53 mice after continuous (circles) and transient (triangles) siRNA treatment. (D) Gross liver images from NRAS G12V / shp53 mice after continuous (top three rows) and transient (bottom three rows) treatment with siRNA. (E) Quantification of surface tumors for NRAS G12V / shp53 mice after continuous (circles) and transient (triangles) siRNA treatment. For panels C and E, the P -values with respect to the PBS group are shown above each group.
    Pt2 Shp53 Gfp4, supplied by Addgene inc, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    siCtnnb1 and siAnln decreased tumor burden in the NRAS G12V / <t>shp53</t> HCC model. (A) Schematic of NRAS G12V / shp53 mouse model receiving continuous siRNA injections. Male C57BL/6J mice underwent HDT injection at 8 weeks of age, i.e. start timepoint of 0 weeks (0w). Injections of siRNA (5 mg/kg) started 4 days later (0.5w) and continued every other week (2.5w, 4.5w, 6.5w). Mice were sacrificed 1 week after the fourth siRNA dose (7.5w). (B) Schematic of NRAS G12V / shp53 mouse model receiving transient siRNA injections. Male C57BL/6J mice underwent HDT injection at 8 weeks of age (0w). Injections of siRNA (5 mg/kg) started 4 days later and continued every other week for a total of two doses (0.5w and 2.5w). Mice were sacrificed 5 weeks after the second siRNA dose (7.5w). (C) Liver-to-body-weight ratios for NRAS G12V / shp53 mice after continuous (circles) and transient (triangles) siRNA treatment. (D) Gross liver images from NRAS G12V / shp53 mice after continuous (top three rows) and transient (bottom three rows) treatment with siRNA. (E) Quantification of surface tumors for NRAS G12V / shp53 mice after continuous (circles) and transient (triangles) siRNA treatment. For panels C and E, the P -values with respect to the PBS group are shown above each group.
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    siCtnnb1 and siAnln decreased tumor burden in the NRAS G12V / <t>shp53</t> HCC model. (A) Schematic of NRAS G12V / shp53 mouse model receiving continuous siRNA injections. Male C57BL/6J mice underwent HDT injection at 8 weeks of age, i.e. start timepoint of 0 weeks (0w). Injections of siRNA (5 mg/kg) started 4 days later (0.5w) and continued every other week (2.5w, 4.5w, 6.5w). Mice were sacrificed 1 week after the fourth siRNA dose (7.5w). (B) Schematic of NRAS G12V / shp53 mouse model receiving transient siRNA injections. Male C57BL/6J mice underwent HDT injection at 8 weeks of age (0w). Injections of siRNA (5 mg/kg) started 4 days later and continued every other week for a total of two doses (0.5w and 2.5w). Mice were sacrificed 5 weeks after the second siRNA dose (7.5w). (C) Liver-to-body-weight ratios for NRAS G12V / shp53 mice after continuous (circles) and transient (triangles) siRNA treatment. (D) Gross liver images from NRAS G12V / shp53 mice after continuous (top three rows) and transient (bottom three rows) treatment with siRNA. (E) Quantification of surface tumors for NRAS G12V / shp53 mice after continuous (circles) and transient (triangles) siRNA treatment. For panels C and E, the P -values with respect to the PBS group are shown above each group.
    Pt2 Shp53 Gfp4 Addgene, supplied by Addgene inc, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    siCtnnb1 and siAnln decreased tumor burden in the NRAS G12V / <t>shp53</t> HCC model. (A) Schematic of NRAS G12V / shp53 mouse model receiving continuous siRNA injections. Male C57BL/6J mice underwent HDT injection at 8 weeks of age, i.e. start timepoint of 0 weeks (0w). Injections of siRNA (5 mg/kg) started 4 days later (0.5w) and continued every other week (2.5w, 4.5w, 6.5w). Mice were sacrificed 1 week after the fourth siRNA dose (7.5w). (B) Schematic of NRAS G12V / shp53 mouse model receiving transient siRNA injections. Male C57BL/6J mice underwent HDT injection at 8 weeks of age (0w). Injections of siRNA (5 mg/kg) started 4 days later and continued every other week for a total of two doses (0.5w and 2.5w). Mice were sacrificed 5 weeks after the second siRNA dose (7.5w). (C) Liver-to-body-weight ratios for NRAS G12V / shp53 mice after continuous (circles) and transient (triangles) siRNA treatment. (D) Gross liver images from NRAS G12V / shp53 mice after continuous (top three rows) and transient (bottom three rows) treatment with siRNA. (E) Quantification of surface tumors for NRAS G12V / shp53 mice after continuous (circles) and transient (triangles) siRNA treatment. For panels C and E, the P -values with respect to the PBS group are shown above each group.
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    Addgene inc pt2 shp53
    siCtnnb1 and siAnln decreased tumor burden in the NRAS G12V / <t>shp53</t> HCC model. (A) Schematic of NRAS G12V / shp53 mouse model receiving continuous siRNA injections. Male C57BL/6J mice underwent HDT injection at 8 weeks of age, i.e. start timepoint of 0 weeks (0w). Injections of siRNA (5 mg/kg) started 4 days later (0.5w) and continued every other week (2.5w, 4.5w, 6.5w). Mice were sacrificed 1 week after the fourth siRNA dose (7.5w). (B) Schematic of NRAS G12V / shp53 mouse model receiving transient siRNA injections. Male C57BL/6J mice underwent HDT injection at 8 weeks of age (0w). Injections of siRNA (5 mg/kg) started 4 days later and continued every other week for a total of two doses (0.5w and 2.5w). Mice were sacrificed 5 weeks after the second siRNA dose (7.5w). (C) Liver-to-body-weight ratios for NRAS G12V / shp53 mice after continuous (circles) and transient (triangles) siRNA treatment. (D) Gross liver images from NRAS G12V / shp53 mice after continuous (top three rows) and transient (bottom three rows) treatment with siRNA. (E) Quantification of surface tumors for NRAS G12V / shp53 mice after continuous (circles) and transient (triangles) siRNA treatment. For panels C and E, the P -values with respect to the PBS group are shown above each group.
    Pt2 Shp53, supplied by Addgene inc, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Figure 4. SNORA13 regulates <t>p53</t> activity through the nucleolar stress response pathway (A) Gene set enrichment analysis (GSEA) showing downregulation of the p53 pathway in SNORA13 knockout BJ-HRASG12V cells at baseline or after tamoxifen treatment. (B) RT-qPCR analysis of CDKN1A expression relative to GAPDH in wild-type BJ-HRASG12V cells or four independent SNORA13 knockout clones at baseline or after tamoxifen treatment. (legend continued on next page)
    Short Hairpin Rna Targeting P53, supplied by Addgene inc, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Image Search Results


    siCtnnb1 and siAnln decreased tumor burden in the NRAS G12V / shp53 HCC model. (A) Schematic of NRAS G12V / shp53 mouse model receiving continuous siRNA injections. Male C57BL/6J mice underwent HDT injection at 8 weeks of age, i.e. start timepoint of 0 weeks (0w). Injections of siRNA (5 mg/kg) started 4 days later (0.5w) and continued every other week (2.5w, 4.5w, 6.5w). Mice were sacrificed 1 week after the fourth siRNA dose (7.5w). (B) Schematic of NRAS G12V / shp53 mouse model receiving transient siRNA injections. Male C57BL/6J mice underwent HDT injection at 8 weeks of age (0w). Injections of siRNA (5 mg/kg) started 4 days later and continued every other week for a total of two doses (0.5w and 2.5w). Mice were sacrificed 5 weeks after the second siRNA dose (7.5w). (C) Liver-to-body-weight ratios for NRAS G12V / shp53 mice after continuous (circles) and transient (triangles) siRNA treatment. (D) Gross liver images from NRAS G12V / shp53 mice after continuous (top three rows) and transient (bottom three rows) treatment with siRNA. (E) Quantification of surface tumors for NRAS G12V / shp53 mice after continuous (circles) and transient (triangles) siRNA treatment. For panels C and E, the P -values with respect to the PBS group are shown above each group.

    Journal: Disease Models & Mechanisms

    Article Title: Chemoprevention of hepatocellular carcinoma using N-acetylgalactosamine-conjugated siRNAs

    doi: 10.1242/dmm.052370

    Figure Lengend Snippet: siCtnnb1 and siAnln decreased tumor burden in the NRAS G12V / shp53 HCC model. (A) Schematic of NRAS G12V / shp53 mouse model receiving continuous siRNA injections. Male C57BL/6J mice underwent HDT injection at 8 weeks of age, i.e. start timepoint of 0 weeks (0w). Injections of siRNA (5 mg/kg) started 4 days later (0.5w) and continued every other week (2.5w, 4.5w, 6.5w). Mice were sacrificed 1 week after the fourth siRNA dose (7.5w). (B) Schematic of NRAS G12V / shp53 mouse model receiving transient siRNA injections. Male C57BL/6J mice underwent HDT injection at 8 weeks of age (0w). Injections of siRNA (5 mg/kg) started 4 days later and continued every other week for a total of two doses (0.5w and 2.5w). Mice were sacrificed 5 weeks after the second siRNA dose (7.5w). (C) Liver-to-body-weight ratios for NRAS G12V / shp53 mice after continuous (circles) and transient (triangles) siRNA treatment. (D) Gross liver images from NRAS G12V / shp53 mice after continuous (top three rows) and transient (bottom three rows) treatment with siRNA. (E) Quantification of surface tumors for NRAS G12V / shp53 mice after continuous (circles) and transient (triangles) siRNA treatment. For panels C and E, the P -values with respect to the PBS group are shown above each group.

    Article Snippet: T/Caggs-NRASV12 ( Addgene plasmid #20205 ) and pT2/shp53/GFP4 ( Addgene plasmid #20208 ) were gifts from John Ohlfest (University of Minnesota, MN, USA).

    Techniques: Injection

    Figure 4. SNORA13 regulates p53 activity through the nucleolar stress response pathway (A) Gene set enrichment analysis (GSEA) showing downregulation of the p53 pathway in SNORA13 knockout BJ-HRASG12V cells at baseline or after tamoxifen treatment. (B) RT-qPCR analysis of CDKN1A expression relative to GAPDH in wild-type BJ-HRASG12V cells or four independent SNORA13 knockout clones at baseline or after tamoxifen treatment. (legend continued on next page)

    Journal: Cell

    Article Title: A non-canonical role for a small nucleolar RNA in ribosome biogenesis and senescence.

    doi: 10.1016/j.cell.2024.06.019

    Figure Lengend Snippet: Figure 4. SNORA13 regulates p53 activity through the nucleolar stress response pathway (A) Gene set enrichment analysis (GSEA) showing downregulation of the p53 pathway in SNORA13 knockout BJ-HRASG12V cells at baseline or after tamoxifen treatment. (B) RT-qPCR analysis of CDKN1A expression relative to GAPDH in wild-type BJ-HRASG12V cells or four independent SNORA13 knockout clones at baseline or after tamoxifen treatment. (legend continued on next page)

    Article Snippet: Male FVB/NJ mice were injected at 7 weeks of age with pT/Caggs-NRASV12 (Addgene #20205),80 SB100 transposase plasmid (pCMV-SB100), and either 1) sgControl plasmid (sgGFP/sgGal4), 2) SNORA13 homolog targeting pool 1 plasmids, 3) SNORA13 homolog targeting pool 2 plasmids, or 4) a Sleeping Beauty plasmid expressing short-hairpin RNA targeting p53 (pT2/shp53/GFP4; Addgene #20208).80 Plasmids were resuspended in 2 mL of saline and administered via tail vein injection in 7 seconds.

    Techniques: Activity Assay, Knock-Out, Quantitative RT-PCR, Expressing, Clone Assay