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renilla luciferase thymidine kinase construct  (Thermo Fisher)
99
Thermo Fisher renilla luciferase thymidine kinase construct
Qu-SeNPs activate WNT and BMP signaling pathways in osteoblasts . ( A ) Transiently transfected MC3T3-E1 cells with Axin-2 and (B) BRE reporter construct were treated free Qu (1 µg mL -1 ) or Qu-SeNPs at equivalent Qu concentration (75 ng mL -1 ) (n = 4; *p<0.05, **p<0.01, ***p<0.001 vs. control; one-way ANOVA with Dunnett’s multiple comparisons test, and # p<0.05, ## p<0.01; unpaired t-test). <t>Luciferase</t> activities were assessed in cell lysates after 48 h and normalized to <t>Renilla</t> luciferase activity, as detailed in the Materials and Methods section. MC3T3-E1 cells were treated with free Qu (1 µg mL -1 ) or Qu-SeNPs at an equivalent Qu concentration (75 ng mL -1 ) for the time indicated in the figure. Protein lysates were subsequently collected. Western blotting revealed the stabilization of (C) β-catenin and the (D) phosphorylation of Smad 1/5/8 molecules. β-actin was a loading control and normalized for densitometric analysis of Western blot bands. The relative expression level is compared to the control (n = 3; *p<0.05, **p<0.01, ***p<0.001 vs. 0 h; one-way ANOVA with Dunnett’s multiple comparisons test, and # p<0.05 vs. free Qu at similar time points; unpaired t-test.
Renilla Luciferase Thymidine Kinase Construct, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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renilla luciferase thymidine kinase construct - by Bioz Stars, 2026-02
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thymidine n1150  (MedChemExpress)
94
MedChemExpress thymidine n1150
Qu-SeNPs activate WNT and BMP signaling pathways in osteoblasts . ( A ) Transiently transfected MC3T3-E1 cells with Axin-2 and (B) BRE reporter construct were treated free Qu (1 µg mL -1 ) or Qu-SeNPs at equivalent Qu concentration (75 ng mL -1 ) (n = 4; *p<0.05, **p<0.01, ***p<0.001 vs. control; one-way ANOVA with Dunnett’s multiple comparisons test, and # p<0.05, ## p<0.01; unpaired t-test). <t>Luciferase</t> activities were assessed in cell lysates after 48 h and normalized to <t>Renilla</t> luciferase activity, as detailed in the Materials and Methods section. MC3T3-E1 cells were treated with free Qu (1 µg mL -1 ) or Qu-SeNPs at an equivalent Qu concentration (75 ng mL -1 ) for the time indicated in the figure. Protein lysates were subsequently collected. Western blotting revealed the stabilization of (C) β-catenin and the (D) phosphorylation of Smad 1/5/8 molecules. β-actin was a loading control and normalized for densitometric analysis of Western blot bands. The relative expression level is compared to the control (n = 3; *p<0.05, **p<0.01, ***p<0.001 vs. 0 h; one-way ANOVA with Dunnett’s multiple comparisons test, and # p<0.05 vs. free Qu at similar time points; unpaired t-test.
Thymidine N1150, supplied by MedChemExpress, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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oligo deoxythymidine primers  (Thermo Fisher)
96
Thermo Fisher oligo deoxythymidine primers
Qu-SeNPs activate WNT and BMP signaling pathways in osteoblasts . ( A ) Transiently transfected MC3T3-E1 cells with Axin-2 and (B) BRE reporter construct were treated free Qu (1 µg mL -1 ) or Qu-SeNPs at equivalent Qu concentration (75 ng mL -1 ) (n = 4; *p<0.05, **p<0.01, ***p<0.001 vs. control; one-way ANOVA with Dunnett’s multiple comparisons test, and # p<0.05, ## p<0.01; unpaired t-test). <t>Luciferase</t> activities were assessed in cell lysates after 48 h and normalized to <t>Renilla</t> luciferase activity, as detailed in the Materials and Methods section. MC3T3-E1 cells were treated with free Qu (1 µg mL -1 ) or Qu-SeNPs at an equivalent Qu concentration (75 ng mL -1 ) for the time indicated in the figure. Protein lysates were subsequently collected. Western blotting revealed the stabilization of (C) β-catenin and the (D) phosphorylation of Smad 1/5/8 molecules. β-actin was a loading control and normalized for densitometric analysis of Western blot bands. The relative expression level is compared to the control (n = 3; *p<0.05, **p<0.01, ***p<0.001 vs. 0 h; one-way ANOVA with Dunnett’s multiple comparisons test, and # p<0.05 vs. free Qu at similar time points; unpaired t-test.
Oligo Deoxythymidine Primers, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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thymidine analog 5 ethynyl  (Thermo Fisher)
96
Thermo Fisher thymidine analog 5 ethynyl
Qu-SeNPs activate WNT and BMP signaling pathways in osteoblasts . ( A ) Transiently transfected MC3T3-E1 cells with Axin-2 and (B) BRE reporter construct were treated free Qu (1 µg mL -1 ) or Qu-SeNPs at equivalent Qu concentration (75 ng mL -1 ) (n = 4; *p<0.05, **p<0.01, ***p<0.001 vs. control; one-way ANOVA with Dunnett’s multiple comparisons test, and # p<0.05, ## p<0.01; unpaired t-test). <t>Luciferase</t> activities were assessed in cell lysates after 48 h and normalized to <t>Renilla</t> luciferase activity, as detailed in the Materials and Methods section. MC3T3-E1 cells were treated with free Qu (1 µg mL -1 ) or Qu-SeNPs at an equivalent Qu concentration (75 ng mL -1 ) for the time indicated in the figure. Protein lysates were subsequently collected. Western blotting revealed the stabilization of (C) β-catenin and the (D) phosphorylation of Smad 1/5/8 molecules. β-actin was a loading control and normalized for densitometric analysis of Western blot bands. The relative expression level is compared to the control (n = 3; *p<0.05, **p<0.01, ***p<0.001 vs. 0 h; one-way ANOVA with Dunnett’s multiple comparisons test, and # p<0.05 vs. free Qu at similar time points; unpaired t-test.
Thymidine Analog 5 Ethynyl, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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thymidine analog 5 bromo  (Thermo Fisher)
96
Thermo Fisher thymidine analog 5 bromo
Qu-SeNPs activate WNT and BMP signaling pathways in osteoblasts . ( A ) Transiently transfected MC3T3-E1 cells with Axin-2 and (B) BRE reporter construct were treated free Qu (1 µg mL -1 ) or Qu-SeNPs at equivalent Qu concentration (75 ng mL -1 ) (n = 4; *p<0.05, **p<0.01, ***p<0.001 vs. control; one-way ANOVA with Dunnett’s multiple comparisons test, and # p<0.05, ## p<0.01; unpaired t-test). <t>Luciferase</t> activities were assessed in cell lysates after 48 h and normalized to <t>Renilla</t> luciferase activity, as detailed in the Materials and Methods section. MC3T3-E1 cells were treated with free Qu (1 µg mL -1 ) or Qu-SeNPs at an equivalent Qu concentration (75 ng mL -1 ) for the time indicated in the figure. Protein lysates were subsequently collected. Western blotting revealed the stabilization of (C) β-catenin and the (D) phosphorylation of Smad 1/5/8 molecules. β-actin was a loading control and normalized for densitometric analysis of Western blot bands. The relative expression level is compared to the control (n = 3; *p<0.05, **p<0.01, ***p<0.001 vs. 0 h; one-way ANOVA with Dunnett’s multiple comparisons test, and # p<0.05 vs. free Qu at similar time points; unpaired t-test.
Thymidine Analog 5 Bromo, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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ht diluted from a 100 × solution of hypoxanthine and thymidine  (Thermo Fisher)
96
Thermo Fisher ht diluted from a 100 × solution of hypoxanthine and thymidine
Qu-SeNPs activate WNT and BMP signaling pathways in osteoblasts . ( A ) Transiently transfected MC3T3-E1 cells with Axin-2 and (B) BRE reporter construct were treated free Qu (1 µg mL -1 ) or Qu-SeNPs at equivalent Qu concentration (75 ng mL -1 ) (n = 4; *p<0.05, **p<0.01, ***p<0.001 vs. control; one-way ANOVA with Dunnett’s multiple comparisons test, and # p<0.05, ## p<0.01; unpaired t-test). <t>Luciferase</t> activities were assessed in cell lysates after 48 h and normalized to <t>Renilla</t> luciferase activity, as detailed in the Materials and Methods section. MC3T3-E1 cells were treated with free Qu (1 µg mL -1 ) or Qu-SeNPs at an equivalent Qu concentration (75 ng mL -1 ) for the time indicated in the figure. Protein lysates were subsequently collected. Western blotting revealed the stabilization of (C) β-catenin and the (D) phosphorylation of Smad 1/5/8 molecules. β-actin was a loading control and normalized for densitometric analysis of Western blot bands. The relative expression level is compared to the control (n = 3; *p<0.05, **p<0.01, ***p<0.001 vs. 0 h; one-way ANOVA with Dunnett’s multiple comparisons test, and # p<0.05 vs. free Qu at similar time points; unpaired t-test.
Ht Diluted From A 100 × Solution Of Hypoxanthine And Thymidine, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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ht diluted from a 100 × solution of hypoxanthine and thymidine - by Bioz Stars, 2026-02
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thymidine analog 5 bromo  (Chem Impex International)
95
Chem Impex International thymidine analog 5 bromo
Qu-SeNPs activate WNT and BMP signaling pathways in osteoblasts . ( A ) Transiently transfected MC3T3-E1 cells with Axin-2 and (B) BRE reporter construct were treated free Qu (1 µg mL -1 ) or Qu-SeNPs at equivalent Qu concentration (75 ng mL -1 ) (n = 4; *p<0.05, **p<0.01, ***p<0.001 vs. control; one-way ANOVA with Dunnett’s multiple comparisons test, and # p<0.05, ## p<0.01; unpaired t-test). <t>Luciferase</t> activities were assessed in cell lysates after 48 h and normalized to <t>Renilla</t> luciferase activity, as detailed in the Materials and Methods section. MC3T3-E1 cells were treated with free Qu (1 µg mL -1 ) or Qu-SeNPs at an equivalent Qu concentration (75 ng mL -1 ) for the time indicated in the figure. Protein lysates were subsequently collected. Western blotting revealed the stabilization of (C) β-catenin and the (D) phosphorylation of Smad 1/5/8 molecules. β-actin was a loading control and normalized for densitometric analysis of Western blot bands. The relative expression level is compared to the control (n = 3; *p<0.05, **p<0.01, ***p<0.001 vs. 0 h; one-way ANOVA with Dunnett’s multiple comparisons test, and # p<0.05 vs. free Qu at similar time points; unpaired t-test.
Thymidine Analog 5 Bromo, supplied by Chem Impex International, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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thymidine analog edu  (Thermo Fisher)
96
Thermo Fisher thymidine analog edu
Qu-SeNPs activate WNT and BMP signaling pathways in osteoblasts . ( A ) Transiently transfected MC3T3-E1 cells with Axin-2 and (B) BRE reporter construct were treated free Qu (1 µg mL -1 ) or Qu-SeNPs at equivalent Qu concentration (75 ng mL -1 ) (n = 4; *p<0.05, **p<0.01, ***p<0.001 vs. control; one-way ANOVA with Dunnett’s multiple comparisons test, and # p<0.05, ## p<0.01; unpaired t-test). <t>Luciferase</t> activities were assessed in cell lysates after 48 h and normalized to <t>Renilla</t> luciferase activity, as detailed in the Materials and Methods section. MC3T3-E1 cells were treated with free Qu (1 µg mL -1 ) or Qu-SeNPs at an equivalent Qu concentration (75 ng mL -1 ) for the time indicated in the figure. Protein lysates were subsequently collected. Western blotting revealed the stabilization of (C) β-catenin and the (D) phosphorylation of Smad 1/5/8 molecules. β-actin was a loading control and normalized for densitometric analysis of Western blot bands. The relative expression level is compared to the control (n = 3; *p<0.05, **p<0.01, ***p<0.001 vs. 0 h; one-way ANOVA with Dunnett’s multiple comparisons test, and # p<0.05 vs. free Qu at similar time points; unpaired t-test.
Thymidine Analog Edu, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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thymidine kinase promoter renilla luciferase reporter plasmid prl tk construct  (Thermo Fisher)
96
Thermo Fisher thymidine kinase promoter renilla luciferase reporter plasmid prl tk construct
Qu-SeNPs activate WNT and BMP signaling pathways in osteoblasts . ( A ) Transiently transfected MC3T3-E1 cells with Axin-2 and (B) BRE reporter construct were treated free Qu (1 µg mL -1 ) or Qu-SeNPs at equivalent Qu concentration (75 ng mL -1 ) (n = 4; *p<0.05, **p<0.01, ***p<0.001 vs. control; one-way ANOVA with Dunnett’s multiple comparisons test, and # p<0.05, ## p<0.01; unpaired t-test). <t>Luciferase</t> activities were assessed in cell lysates after 48 h and normalized to <t>Renilla</t> luciferase activity, as detailed in the Materials and Methods section. MC3T3-E1 cells were treated with free Qu (1 µg mL -1 ) or Qu-SeNPs at an equivalent Qu concentration (75 ng mL -1 ) for the time indicated in the figure. Protein lysates were subsequently collected. Western blotting revealed the stabilization of (C) β-catenin and the (D) phosphorylation of Smad 1/5/8 molecules. β-actin was a loading control and normalized for densitometric analysis of Western blot bands. The relative expression level is compared to the control (n = 3; *p<0.05, **p<0.01, ***p<0.001 vs. 0 h; one-way ANOVA with Dunnett’s multiple comparisons test, and # p<0.05 vs. free Qu at similar time points; unpaired t-test.
Thymidine Kinase Promoter Renilla Luciferase Reporter Plasmid Prl Tk Construct, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Image Search Results


Qu-SeNPs activate WNT and BMP signaling pathways in osteoblasts . ( A ) Transiently transfected MC3T3-E1 cells with Axin-2 and (B) BRE reporter construct were treated free Qu (1 µg mL -1 ) or Qu-SeNPs at equivalent Qu concentration (75 ng mL -1 ) (n = 4; *p<0.05, **p<0.01, ***p<0.001 vs. control; one-way ANOVA with Dunnett’s multiple comparisons test, and # p<0.05, ## p<0.01; unpaired t-test). Luciferase activities were assessed in cell lysates after 48 h and normalized to Renilla luciferase activity, as detailed in the Materials and Methods section. MC3T3-E1 cells were treated with free Qu (1 µg mL -1 ) or Qu-SeNPs at an equivalent Qu concentration (75 ng mL -1 ) for the time indicated in the figure. Protein lysates were subsequently collected. Western blotting revealed the stabilization of (C) β-catenin and the (D) phosphorylation of Smad 1/5/8 molecules. β-actin was a loading control and normalized for densitometric analysis of Western blot bands. The relative expression level is compared to the control (n = 3; *p<0.05, **p<0.01, ***p<0.001 vs. 0 h; one-way ANOVA with Dunnett’s multiple comparisons test, and # p<0.05 vs. free Qu at similar time points; unpaired t-test.

Journal: Aging and Disease

Article Title: Bone Regeneration Enhanced by Quercetin-Capped Selenium Nanoparticles via miR206/Connexin43, WNT, and BMP signaling pathways

doi: 10.14336/AD.2025.0025

Figure Lengend Snippet: Qu-SeNPs activate WNT and BMP signaling pathways in osteoblasts . ( A ) Transiently transfected MC3T3-E1 cells with Axin-2 and (B) BRE reporter construct were treated free Qu (1 µg mL -1 ) or Qu-SeNPs at equivalent Qu concentration (75 ng mL -1 ) (n = 4; *p<0.05, **p<0.01, ***p<0.001 vs. control; one-way ANOVA with Dunnett’s multiple comparisons test, and # p<0.05, ## p<0.01; unpaired t-test). Luciferase activities were assessed in cell lysates after 48 h and normalized to Renilla luciferase activity, as detailed in the Materials and Methods section. MC3T3-E1 cells were treated with free Qu (1 µg mL -1 ) or Qu-SeNPs at an equivalent Qu concentration (75 ng mL -1 ) for the time indicated in the figure. Protein lysates were subsequently collected. Western blotting revealed the stabilization of (C) β-catenin and the (D) phosphorylation of Smad 1/5/8 molecules. β-actin was a loading control and normalized for densitometric analysis of Western blot bands. The relative expression level is compared to the control (n = 3; *p<0.05, **p<0.01, ***p<0.001 vs. 0 h; one-way ANOVA with Dunnett’s multiple comparisons test, and # p<0.05 vs. free Qu at similar time points; unpaired t-test.

Article Snippet: Trizol reagent, SuperScript ІІ Reverse Transcriptase, and Renilla luciferase thymidine kinase construct was purchased from Invitrogen, USA.

Techniques: Protein-Protein interactions, Transfection, Construct, Concentration Assay, Control, Luciferase, Activity Assay, Western Blot, Phospho-proteomics, Expressing