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prk5 egfp tau plasmid wt 0n4r  (Addgene inc)


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    Structured Review

    Addgene inc prk5 egfp tau plasmid wt 0n4r
    Prk5 Egfp Tau Plasmid Wt 0n4r, supplied by Addgene inc, used in various techniques. Bioz Stars score: 93/100, based on 73 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/prk5+egfp+tau+wt/pRK5-EGFP-Tau+(Plasmid+%2346904)/10__1016_slash_j__dscb__2025__100236-68-5-14
    Average 93 stars, based on 73 article reviews
    prk5 egfp tau plasmid wt 0n4r - by Bioz Stars, 2026-09
    93/100 stars

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    Related Articles

    Amplification:

    Article Title: Tau induces PSD95-nNOS uncoupling and neurovascular dysfunction independent of neurodegeneration
    Article Snippet: Filters were washed 4 times for 2min in 0.5% phosphoric acid, and the remaining radioactivity was quantified in a LS3801 scintillation counter (Beckman Coulter) by the Cherenkov method. .. PSD95 was amplified from C57BL6/J mouse cDNA with primers containing Eco RI (5’- gcacGAATTCatatggactgtctctgtatagtg-3’) and Xho I (5’-gataCTCGAGtcagagtctctctcgggctgg-3’) restriction sites and subsequently cloned into Eco RI/ Xho I-digested pCMV-Myc vector (Clontech). pcDNA3.1-nNOS , pRK5-EGFP-Tau WT and pRK5-EGFP-Tau P301L were kind gifts from Yoichi Osawa (University of Michigan Medical School, Ann Arbor, MI) and Karen Ashe (Addgene plasmid #46904 and #46908; University of Minnesota, Minneapolis, MN), respectively. pcDNA3.1 (Thermo Fisher Scientific) and pEGFP-C3 (Clontech) plasmids were used as empty vector expression controls. ..

    Clone Assay:

    Article Title: Tau induces PSD95-nNOS uncoupling and neurovascular dysfunction independent of neurodegeneration
    Article Snippet: Filters were washed 4 times for 2min in 0.5% phosphoric acid, and the remaining radioactivity was quantified in a LS3801 scintillation counter (Beckman Coulter) by the Cherenkov method. .. PSD95 was amplified from C57BL6/J mouse cDNA with primers containing Eco RI (5’- gcacGAATTCatatggactgtctctgtatagtg-3’) and Xho I (5’-gataCTCGAGtcagagtctctctcgggctgg-3’) restriction sites and subsequently cloned into Eco RI/ Xho I-digested pCMV-Myc vector (Clontech). pcDNA3.1-nNOS , pRK5-EGFP-Tau WT and pRK5-EGFP-Tau P301L were kind gifts from Yoichi Osawa (University of Michigan Medical School, Ann Arbor, MI) and Karen Ashe (Addgene plasmid #46904 and #46908; University of Minnesota, Minneapolis, MN), respectively. pcDNA3.1 (Thermo Fisher Scientific) and pEGFP-C3 (Clontech) plasmids were used as empty vector expression controls. ..

    Plasmid Preparation:

    Article Title: Tau induces PSD95-nNOS uncoupling and neurovascular dysfunction independent of neurodegeneration
    Article Snippet: Filters were washed 4 times for 2min in 0.5% phosphoric acid, and the remaining radioactivity was quantified in a LS3801 scintillation counter (Beckman Coulter) by the Cherenkov method. .. PSD95 was amplified from C57BL6/J mouse cDNA with primers containing Eco RI (5’- gcacGAATTCatatggactgtctctgtatagtg-3’) and Xho I (5’-gataCTCGAGtcagagtctctctcgggctgg-3’) restriction sites and subsequently cloned into Eco RI/ Xho I-digested pCMV-Myc vector (Clontech). pcDNA3.1-nNOS , pRK5-EGFP-Tau WT and pRK5-EGFP-Tau P301L were kind gifts from Yoichi Osawa (University of Michigan Medical School, Ann Arbor, MI) and Karen Ashe (Addgene plasmid #46904 and #46908; University of Minnesota, Minneapolis, MN), respectively. pcDNA3.1 (Thermo Fisher Scientific) and pEGFP-C3 (Clontech) plasmids were used as empty vector expression controls. ..

    Article Title: Tau Misfolding Efficiently Propagates between Individual Intact Hippocampal Neurons
    Article Snippet: .. The following plasmids were used: pRFP-N1, pEGFP-C3 (Clontech); pRK5-EGFP-tau WT and pRK5-EGFP-tau E14 were a gift from Karen Ashe ( Hoover et al., 2010 ; Addgene, plasmids #46904 and #46907); GCaMP6 was a gift from Douglas Kim ( Chen et al., 2013 ; Addgene, plasmid #40753); and R-GECO was a gift from Robert Campbell ( J. Wu et al., 2013 ; Addgene, plasmid #45494). ..

    Article Title: Efficient propagation of misfolded tau between individual neurons occurs in absence of degeneration
    Article Snippet: .. The following plasmids were used: pRFP-N1, pEGFP-C3 (Clontech), pRK5-EGFP-tau WT and pRK5-EGFP-tau E14 were a gift from Karen Ashe (Addgene plasmids #46904 and #46907), GCaMP6 was a gift from Douglas Kim (Addgene plasmid #40753), R-GECO was a gift from Robert Campbell (Addgene plasmid #45494). ..

    Expressing:

    Article Title: Tau induces PSD95-nNOS uncoupling and neurovascular dysfunction independent of neurodegeneration
    Article Snippet: Filters were washed 4 times for 2min in 0.5% phosphoric acid, and the remaining radioactivity was quantified in a LS3801 scintillation counter (Beckman Coulter) by the Cherenkov method. .. PSD95 was amplified from C57BL6/J mouse cDNA with primers containing Eco RI (5’- gcacGAATTCatatggactgtctctgtatagtg-3’) and Xho I (5’-gataCTCGAGtcagagtctctctcgggctgg-3’) restriction sites and subsequently cloned into Eco RI/ Xho I-digested pCMV-Myc vector (Clontech). pcDNA3.1-nNOS , pRK5-EGFP-Tau WT and pRK5-EGFP-Tau P301L were kind gifts from Yoichi Osawa (University of Michigan Medical School, Ann Arbor, MI) and Karen Ashe (Addgene plasmid #46904 and #46908; University of Minnesota, Minneapolis, MN), respectively. pcDNA3.1 (Thermo Fisher Scientific) and pEGFP-C3 (Clontech) plasmids were used as empty vector expression controls. ..



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    DIPQUO blocks phosphorylation of tau microtubule-associated protein . A , NIH/3T3 fibroblasts were transfected with GFP-tagged human four-repeat WT tau <t>(4R0N)</t> and treated with 500 nM AZD or 10 μM DIPQUO for 24 h and then analyzed by Western blotting for tau expression and activity via phosphorylation of S396. Phospho-S396-tau was quantified as a ratio to total tau in the graph at right. Values are reported as the means ± SD; ∗ p < 0.05 in unpaired two-tailed Student's t test. Ordinary one-way ANOVA yielded F = 10.12 and p = 0.0119. B , further dose–response Western blotting analysis of tau S396 phosphorylation demonstrated a dose-dependent relationship for DIPQUO, with significant inhibition at the 500 nM dose. Values are reported as the means ± SD; ∗ p < 0.05 and ∗∗ p < 0.01 in unpaired two-tailed Student's t test. Ordinary one-way ANOVA yielded F = 7.549 and p = 0.0020. C , phosphorylation of tau S396 and T217 was analyzed after treatment with DIPQUO in the absence or presence of the ERK1/2 inhibitor UO126. Phospho-tau was quantified in the graph as a ratio to total tau, normalized to β-actin, with P-tau-S396 in black and P-tau-T217 in blue . Values are reported as the means ± SD; ∗ p < 0.05 in unpaired two-tailed Student's t test. Two-way ANOVA yielded F = 1.235 and p = 0.3296. D , depletion of GSK3-β for 24 h with siRNA partially restored S396 phosphorylation of tau after an additional 24 h of 10 μM DIPQUO treatment. The graph at right shows ratio of phospho-S396-tau to total tau, normalized to β-actin protein loading control. Values are reported as the means ± SD; ∗ p < 0.05 and ∗∗∗∗ p < 0.0001 in unpaired two-tailed Student's t test. Ordinary one-way ANOVA yielded F = 15.61 and p < 0.0001. Representative images from experiments using at least three biological replicates are shown for all figure panels. AZD, AstraZeneca GSK3-β-specific inhibitor AZD2858; GSK3-β, glycogen synthase kinase 3-beta.
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    Image Search Results


    DIPQUO blocks phosphorylation of tau microtubule-associated protein . A , NIH/3T3 fibroblasts were transfected with GFP-tagged human four-repeat WT tau (4R0N) and treated with 500 nM AZD or 10 μM DIPQUO for 24 h and then analyzed by Western blotting for tau expression and activity via phosphorylation of S396. Phospho-S396-tau was quantified as a ratio to total tau in the graph at right. Values are reported as the means ± SD; ∗ p < 0.05 in unpaired two-tailed Student's t test. Ordinary one-way ANOVA yielded F = 10.12 and p = 0.0119. B , further dose–response Western blotting analysis of tau S396 phosphorylation demonstrated a dose-dependent relationship for DIPQUO, with significant inhibition at the 500 nM dose. Values are reported as the means ± SD; ∗ p < 0.05 and ∗∗ p < 0.01 in unpaired two-tailed Student's t test. Ordinary one-way ANOVA yielded F = 7.549 and p = 0.0020. C , phosphorylation of tau S396 and T217 was analyzed after treatment with DIPQUO in the absence or presence of the ERK1/2 inhibitor UO126. Phospho-tau was quantified in the graph as a ratio to total tau, normalized to β-actin, with P-tau-S396 in black and P-tau-T217 in blue . Values are reported as the means ± SD; ∗ p < 0.05 in unpaired two-tailed Student's t test. Two-way ANOVA yielded F = 1.235 and p = 0.3296. D , depletion of GSK3-β for 24 h with siRNA partially restored S396 phosphorylation of tau after an additional 24 h of 10 μM DIPQUO treatment. The graph at right shows ratio of phospho-S396-tau to total tau, normalized to β-actin protein loading control. Values are reported as the means ± SD; ∗ p < 0.05 and ∗∗∗∗ p < 0.0001 in unpaired two-tailed Student's t test. Ordinary one-way ANOVA yielded F = 15.61 and p < 0.0001. Representative images from experiments using at least three biological replicates are shown for all figure panels. AZD, AstraZeneca GSK3-β-specific inhibitor AZD2858; GSK3-β, glycogen synthase kinase 3-beta.

    Journal: The Journal of Biological Chemistry

    Article Title: The small molecule DIPQUO promotes osteogenic differentiation via inhibition of glycogen synthase kinase 3-beta signaling

    doi: 10.1016/j.jbc.2021.100696

    Figure Lengend Snippet: DIPQUO blocks phosphorylation of tau microtubule-associated protein . A , NIH/3T3 fibroblasts were transfected with GFP-tagged human four-repeat WT tau (4R0N) and treated with 500 nM AZD or 10 μM DIPQUO for 24 h and then analyzed by Western blotting for tau expression and activity via phosphorylation of S396. Phospho-S396-tau was quantified as a ratio to total tau in the graph at right. Values are reported as the means ± SD; ∗ p < 0.05 in unpaired two-tailed Student's t test. Ordinary one-way ANOVA yielded F = 10.12 and p = 0.0119. B , further dose–response Western blotting analysis of tau S396 phosphorylation demonstrated a dose-dependent relationship for DIPQUO, with significant inhibition at the 500 nM dose. Values are reported as the means ± SD; ∗ p < 0.05 and ∗∗ p < 0.01 in unpaired two-tailed Student's t test. Ordinary one-way ANOVA yielded F = 7.549 and p = 0.0020. C , phosphorylation of tau S396 and T217 was analyzed after treatment with DIPQUO in the absence or presence of the ERK1/2 inhibitor UO126. Phospho-tau was quantified in the graph as a ratio to total tau, normalized to β-actin, with P-tau-S396 in black and P-tau-T217 in blue . Values are reported as the means ± SD; ∗ p < 0.05 in unpaired two-tailed Student's t test. Two-way ANOVA yielded F = 1.235 and p = 0.3296. D , depletion of GSK3-β for 24 h with siRNA partially restored S396 phosphorylation of tau after an additional 24 h of 10 μM DIPQUO treatment. The graph at right shows ratio of phospho-S396-tau to total tau, normalized to β-actin protein loading control. Values are reported as the means ± SD; ∗ p < 0.05 and ∗∗∗∗ p < 0.0001 in unpaired two-tailed Student's t test. Ordinary one-way ANOVA yielded F = 15.61 and p < 0.0001. Representative images from experiments using at least three biological replicates are shown for all figure panels. AZD, AstraZeneca GSK3-β-specific inhibitor AZD2858; GSK3-β, glycogen synthase kinase 3-beta.

    Article Snippet: An expression construct containing 4-repeat human WT 4R0N tau (pRK5-EGFP-tau, Addgene 46904) was transfected into 70% confluent NIH/3T3 cells using Lipofectamine LTX Plus reagent (Invitrogen 15338-100), and DIPQUO or inhibitor treatments were performed simultaneously.

    Techniques: Phospho-proteomics, Transfection, Western Blot, Expressing, Activity Assay, Two Tailed Test, Inhibition, Control