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ii one step cloning kit  (Vazyme Biotech Co)


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    Structured Review

    Vazyme Biotech Co ii one step cloning kit
    Ii One Step Cloning Kit, supplied by Vazyme Biotech Co, used in various techniques. Bioz Stars score: 99/100, based on 6252 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/step+kit/ClonExpress+II+One+Step+Cloning+Kit/pmc13090716-105-13-18
    Average 99 stars, based on 6252 article reviews
    ii one step cloning kit - by Bioz Stars, 2026-09
    99/100 stars

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    Related Articles

    Clone Assay:

    Article Title: Heterogeneous expression of human PNPLA3 triggers algal lipid accumulation and lipid droplet enlargement
    Article Snippet: Microalgal metabolic engineering holds great promise for algal biofuels.. However, identification of the key lipid metabolic target remains challenging due to its complex regulation.. In this study, we advocated an alternative strategy that potentially rewired lipid metabolism by unprecedented mechanisms.

    Article Title: Crucial carotenogenic genes elevate hyperaccumulation of both fucoxanthin and β-carotene in Phaeodactylum tricornutum
    Article Snippet: Burgeoning demand for carotenoids from natural resources has urged to explore the promising metabolic engineering strategy to improve algal systems.. However, existing biological intricacies in algal carotenogenesis warrant identification and exploitation of potential molecular candidate(s) for metabolic engineering to exploit the maximum potential of microalgal cell factories.. Here, we identified two critical carotenogenic genes, including 1-deoxy-D-xylulose 5-phosphate synthase and lycopene cyclase and concurrently overexpressed in Phaeodactylum tricornutum.

    Article Title: Cystatin B Attenuates Cerebral Ischemia Reperfusion Injury by Inhibiting the JAK2/STAT3 Signaling Pathway.
    Article Snippet: .. For overexpression, the mouse Cstb coding sequence was amplified with Phanta Max Super- Fidelity DNA Polymerase (P505- d1, Vazyme) and cloned into the pHAGE vector using the ClonExpress II one- step kit (C112- 02, Vazyme) to generate the pHAGE- CMV- Cstb- Flag- PGK- puro plasmid (designated Flag- Cstb; empty vector served as Flag control). .. Both recombinant plasmids were then co- transfected with the packaging plasmids pMD2.G and psPAX2 into HEK293T cells using polyethyleneimine (PEI; 23966- 1, Polysciences).

    Article Title: Occurrence of plastidial triacylglycerol synthesis and the potential regulatory role of AGPAT in the model diatom Phaeodactylum tricornutum
    Article Snippet: .. The fragment of AGPAT1 was purified by TaKaRa MiniBEST DNA Fragment Purification Kit (Takara, Japan) and the PtAGPAT1 coding sequence was cloned in between the fucoxanthin chlorophyll a/c binding protein (fcp) PfcpC promoter and TfcpA terminator in the expression vector pHY-18 [ ] by ClonExpress II one step kit (Vazyme, China) according to the manufacturer’s protocol. ..

    Expressing:

    Article Title: Heterogeneous expression of human PNPLA3 triggers algal lipid accumulation and lipid droplet enlargement
    Article Snippet: Microalgal metabolic engineering holds great promise for algal biofuels.. However, identification of the key lipid metabolic target remains challenging due to its complex regulation.. In this study, we advocated an alternative strategy that potentially rewired lipid metabolism by unprecedented mechanisms.

    Article Title: Crucial carotenogenic genes elevate hyperaccumulation of both fucoxanthin and β-carotene in Phaeodactylum tricornutum
    Article Snippet: Burgeoning demand for carotenoids from natural resources has urged to explore the promising metabolic engineering strategy to improve algal systems.. However, existing biological intricacies in algal carotenogenesis warrant identification and exploitation of potential molecular candidate(s) for metabolic engineering to exploit the maximum potential of microalgal cell factories.. Here, we identified two critical carotenogenic genes, including 1-deoxy-D-xylulose 5-phosphate synthase and lycopene cyclase and concurrently overexpressed in Phaeodactylum tricornutum.

    Article Title: Characterization of the main immunogenic proteins in Brucella infection for their application in diagnosis of brucellosis.
    Article Snippet: Brucellosis is an important zoonotic bacterial disease widespread in the world.. The key step of control this disease is accurate diagnosis and elimination of diseased animals.. The classic diagnostic methods, such as tube agglutination test, are inaccurate and nonspecific, because of cross-reaction with Yersinia enterocolitica serotype O:9.

    Article Title: Occurrence of plastidial triacylglycerol synthesis and the potential regulatory role of AGPAT in the model diatom Phaeodactylum tricornutum
    Article Snippet: .. The fragment of AGPAT1 was purified by TaKaRa MiniBEST DNA Fragment Purification Kit (Takara, Japan) and the PtAGPAT1 coding sequence was cloned in between the fucoxanthin chlorophyll a/c binding protein (fcp) PfcpC promoter and TfcpA terminator in the expression vector pHY-18 [ ] by ClonExpress II one step kit (Vazyme, China) according to the manufacturer’s protocol. ..

    Plasmid Preparation:

    Article Title: Heterogeneous expression of human PNPLA3 triggers algal lipid accumulation and lipid droplet enlargement
    Article Snippet: Microalgal metabolic engineering holds great promise for algal biofuels.. However, identification of the key lipid metabolic target remains challenging due to its complex regulation.. In this study, we advocated an alternative strategy that potentially rewired lipid metabolism by unprecedented mechanisms.

    Article Title: Crucial carotenogenic genes elevate hyperaccumulation of both fucoxanthin and β-carotene in Phaeodactylum tricornutum
    Article Snippet: Burgeoning demand for carotenoids from natural resources has urged to explore the promising metabolic engineering strategy to improve algal systems.. However, existing biological intricacies in algal carotenogenesis warrant identification and exploitation of potential molecular candidate(s) for metabolic engineering to exploit the maximum potential of microalgal cell factories.. Here, we identified two critical carotenogenic genes, including 1-deoxy-D-xylulose 5-phosphate synthase and lycopene cyclase and concurrently overexpressed in Phaeodactylum tricornutum.

    Article Title: A rough Brucella mutant induced macrophage death depends on secretion activity of T4SS, but not on cellular Txnip- and Caspase-2-mediated signaling pathway.
    Article Snippet: Brucella is a facultative intracellular bacterium, dividing into smoothand rough-type Brucella.. Smooth-type Brucella can dissociate into rough mutants with cytotoxicity for macrophages during infection, which is critical for Brucella egress and dissemination.. However, the mechanism of cytotoxicity infected by rough Brucella is incomplete.

    Article Title: Cystatin B Attenuates Cerebral Ischemia Reperfusion Injury by Inhibiting the JAK2/STAT3 Signaling Pathway.
    Article Snippet: .. For overexpression, the mouse Cstb coding sequence was amplified with Phanta Max Super- Fidelity DNA Polymerase (P505- d1, Vazyme) and cloned into the pHAGE vector using the ClonExpress II one- step kit (C112- 02, Vazyme) to generate the pHAGE- CMV- Cstb- Flag- PGK- puro plasmid (designated Flag- Cstb; empty vector served as Flag control). .. Both recombinant plasmids were then co- transfected with the packaging plasmids pMD2.G and psPAX2 into HEK293T cells using polyethyleneimine (PEI; 23966- 1, Polysciences).

    Article Title: Occurrence of plastidial triacylglycerol synthesis and the potential regulatory role of AGPAT in the model diatom Phaeodactylum tricornutum
    Article Snippet: .. The fragment of AGPAT1 was purified by TaKaRa MiniBEST DNA Fragment Purification Kit (Takara, Japan) and the PtAGPAT1 coding sequence was cloned in between the fucoxanthin chlorophyll a/c binding protein (fcp) PfcpC promoter and TfcpA terminator in the expression vector pHY-18 [ ] by ClonExpress II one step kit (Vazyme, China) according to the manufacturer’s protocol. ..

    Homologous Recombination:

    Article Title: Heterogeneous expression of human PNPLA3 triggers algal lipid accumulation and lipid droplet enlargement
    Article Snippet: Microalgal metabolic engineering holds great promise for algal biofuels.. However, identification of the key lipid metabolic target remains challenging due to its complex regulation.. In this study, we advocated an alternative strategy that potentially rewired lipid metabolism by unprecedented mechanisms.

    Purification:

    Article Title: Crucial carotenogenic genes elevate hyperaccumulation of both fucoxanthin and β-carotene in Phaeodactylum tricornutum
    Article Snippet: Burgeoning demand for carotenoids from natural resources has urged to explore the promising metabolic engineering strategy to improve algal systems.. However, existing biological intricacies in algal carotenogenesis warrant identification and exploitation of potential molecular candidate(s) for metabolic engineering to exploit the maximum potential of microalgal cell factories.. Here, we identified two critical carotenogenic genes, including 1-deoxy-D-xylulose 5-phosphate synthase and lycopene cyclase and concurrently overexpressed in Phaeodactylum tricornutum.

    Article Title: Occurrence of plastidial triacylglycerol synthesis and the potential regulatory role of AGPAT in the model diatom Phaeodactylum tricornutum
    Article Snippet: .. The fragment of AGPAT1 was purified by TaKaRa MiniBEST DNA Fragment Purification Kit (Takara, Japan) and the PtAGPAT1 coding sequence was cloned in between the fucoxanthin chlorophyll a/c binding protein (fcp) PfcpC promoter and TfcpA terminator in the expression vector pHY-18 [ ] by ClonExpress II one step kit (Vazyme, China) according to the manufacturer’s protocol. ..

    Binding Assay:

    Article Title: Crucial carotenogenic genes elevate hyperaccumulation of both fucoxanthin and β-carotene in Phaeodactylum tricornutum
    Article Snippet: Burgeoning demand for carotenoids from natural resources has urged to explore the promising metabolic engineering strategy to improve algal systems.. However, existing biological intricacies in algal carotenogenesis warrant identification and exploitation of potential molecular candidate(s) for metabolic engineering to exploit the maximum potential of microalgal cell factories.. Here, we identified two critical carotenogenic genes, including 1-deoxy-D-xylulose 5-phosphate synthase and lycopene cyclase and concurrently overexpressed in Phaeodactylum tricornutum.

    Article Title: Occurrence of plastidial triacylglycerol synthesis and the potential regulatory role of AGPAT in the model diatom Phaeodactylum tricornutum
    Article Snippet: .. The fragment of AGPAT1 was purified by TaKaRa MiniBEST DNA Fragment Purification Kit (Takara, Japan) and the PtAGPAT1 coding sequence was cloned in between the fucoxanthin chlorophyll a/c binding protein (fcp) PfcpC promoter and TfcpA terminator in the expression vector pHY-18 [ ] by ClonExpress II one step kit (Vazyme, China) according to the manufacturer’s protocol. ..

    Cloning:

    Article Title: Characterization of the main immunogenic proteins in Brucella infection for their application in diagnosis of brucellosis.
    Article Snippet: Brucellosis is an important zoonotic bacterial disease widespread in the world.. The key step of control this disease is accurate diagnosis and elimination of diseased animals.. The classic diagnostic methods, such as tube agglutination test, are inaccurate and nonspecific, because of cross-reaction with Yersinia enterocolitica serotype O:9.

    Protein Purification:

    Article Title: Characterization of the main immunogenic proteins in Brucella infection for their application in diagnosis of brucellosis.
    Article Snippet: Brucellosis is an important zoonotic bacterial disease widespread in the world.. The key step of control this disease is accurate diagnosis and elimination of diseased animals.. The classic diagnostic methods, such as tube agglutination test, are inaccurate and nonspecific, because of cross-reaction with Yersinia enterocolitica serotype O:9.

    Bacteria:

    Article Title: Characterization of the main immunogenic proteins in Brucella infection for their application in diagnosis of brucellosis.
    Article Snippet: Brucellosis is an important zoonotic bacterial disease widespread in the world.. The key step of control this disease is accurate diagnosis and elimination of diseased animals.. The classic diagnostic methods, such as tube agglutination test, are inaccurate and nonspecific, because of cross-reaction with Yersinia enterocolitica serotype O:9.

    Polymerase Chain Reaction:

    Article Title: Characterization of the main immunogenic proteins in Brucella infection for their application in diagnosis of brucellosis.
    Article Snippet: Brucellosis is an important zoonotic bacterial disease widespread in the world.. The key step of control this disease is accurate diagnosis and elimination of diseased animals.. The classic diagnostic methods, such as tube agglutination test, are inaccurate and nonspecific, because of cross-reaction with Yersinia enterocolitica serotype O:9.

    Article Title: A rough Brucella mutant induced macrophage death depends on secretion activity of T4SS, but not on cellular Txnip- and Caspase-2-mediated signaling pathway.
    Article Snippet: Brucella is a facultative intracellular bacterium, dividing into smoothand rough-type Brucella.. Smooth-type Brucella can dissociate into rough mutants with cytotoxicity for macrophages during infection, which is critical for Brucella egress and dissemination.. However, the mechanism of cytotoxicity infected by rough Brucella is incomplete.

    Amplification:

    Article Title: A rough Brucella mutant induced macrophage death depends on secretion activity of T4SS, but not on cellular Txnip- and Caspase-2-mediated signaling pathway.
    Article Snippet: Brucella is a facultative intracellular bacterium, dividing into smoothand rough-type Brucella.. Smooth-type Brucella can dissociate into rough mutants with cytotoxicity for macrophages during infection, which is critical for Brucella egress and dissemination.. However, the mechanism of cytotoxicity infected by rough Brucella is incomplete.

    Article Title: Cystatin B Attenuates Cerebral Ischemia Reperfusion Injury by Inhibiting the JAK2/STAT3 Signaling Pathway.
    Article Snippet: .. For overexpression, the mouse Cstb coding sequence was amplified with Phanta Max Super- Fidelity DNA Polymerase (P505- d1, Vazyme) and cloned into the pHAGE vector using the ClonExpress II one- step kit (C112- 02, Vazyme) to generate the pHAGE- CMV- Cstb- Flag- PGK- puro plasmid (designated Flag- Cstb; empty vector served as Flag control). .. Both recombinant plasmids were then co- transfected with the packaging plasmids pMD2.G and psPAX2 into HEK293T cells using polyethyleneimine (PEI; 23966- 1, Polysciences).

    Over Expression:

    Article Title: Cystatin B Attenuates Cerebral Ischemia Reperfusion Injury by Inhibiting the JAK2/STAT3 Signaling Pathway.
    Article Snippet: .. For overexpression, the mouse Cstb coding sequence was amplified with Phanta Max Super- Fidelity DNA Polymerase (P505- d1, Vazyme) and cloned into the pHAGE vector using the ClonExpress II one- step kit (C112- 02, Vazyme) to generate the pHAGE- CMV- Cstb- Flag- PGK- puro plasmid (designated Flag- Cstb; empty vector served as Flag control). .. Both recombinant plasmids were then co- transfected with the packaging plasmids pMD2.G and psPAX2 into HEK293T cells using polyethyleneimine (PEI; 23966- 1, Polysciences).

    Sequencing:

    Article Title: Cystatin B Attenuates Cerebral Ischemia Reperfusion Injury by Inhibiting the JAK2/STAT3 Signaling Pathway.
    Article Snippet: .. For overexpression, the mouse Cstb coding sequence was amplified with Phanta Max Super- Fidelity DNA Polymerase (P505- d1, Vazyme) and cloned into the pHAGE vector using the ClonExpress II one- step kit (C112- 02, Vazyme) to generate the pHAGE- CMV- Cstb- Flag- PGK- puro plasmid (designated Flag- Cstb; empty vector served as Flag control). .. Both recombinant plasmids were then co- transfected with the packaging plasmids pMD2.G and psPAX2 into HEK293T cells using polyethyleneimine (PEI; 23966- 1, Polysciences).

    Article Title: Occurrence of plastidial triacylglycerol synthesis and the potential regulatory role of AGPAT in the model diatom Phaeodactylum tricornutum
    Article Snippet: .. The fragment of AGPAT1 was purified by TaKaRa MiniBEST DNA Fragment Purification Kit (Takara, Japan) and the PtAGPAT1 coding sequence was cloned in between the fucoxanthin chlorophyll a/c binding protein (fcp) PfcpC promoter and TfcpA terminator in the expression vector pHY-18 [ ] by ClonExpress II one step kit (Vazyme, China) according to the manufacturer’s protocol. ..

    Control:

    Article Title: Cystatin B Attenuates Cerebral Ischemia Reperfusion Injury by Inhibiting the JAK2/STAT3 Signaling Pathway.
    Article Snippet: .. For overexpression, the mouse Cstb coding sequence was amplified with Phanta Max Super- Fidelity DNA Polymerase (P505- d1, Vazyme) and cloned into the pHAGE vector using the ClonExpress II one- step kit (C112- 02, Vazyme) to generate the pHAGE- CMV- Cstb- Flag- PGK- puro plasmid (designated Flag- Cstb; empty vector served as Flag control). .. Both recombinant plasmids were then co- transfected with the packaging plasmids pMD2.G and psPAX2 into HEK293T cells using polyethyleneimine (PEI; 23966- 1, Polysciences).



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    Image Search Results


    Roles of the CD39/CD73 axis on DUB's multidirectional protection effects in Dex-treated primary BMSCs. ( A ) ELISA for ROS clearance-related enzyme T-SOD and ROS damage biomarkers 8-OHdG, AOPP, and MDA in primary BMSCs of different groups. ( B ) Western blot and quantification for the expression of ROS clearance-related proteins in primary BMSCs of different groups. ( C ) Representative images and quantitative analysis of immunofluorescence staining for MitoSox (red) in primary BMSCs of different groups, and nuclei were stained with Hoechst (blue). ( D ) Western blot and quantification for the expression of apoptosis-related proteins in primary BMSCs of different groups. ( E ) Cellular apoptosis detection in primary BMSCs of different groups by Annexin V-FITC and PI dual-staining assessment via flow cytometry. The proportion of cells in each quadrant was indicated in the plot. ( F ) Tunel (red) staining and quantification of apoptotic cells in primary BMSCs of different groups, and nuclei were stained with DAPI (blue). ( G ) Representative images and quantitative analysis of Alizarin Red S staining for mineralization in primary BMSCs of different groups under osteogenic conditions. ( H ) Western blot and quantification for the expression of osteogenesis-related proteins in primary BMSCs of different groups. n = 4 independent repeats by using different biological samples in each group for in vitro experiments. Data were means ± s.e.m. ∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗ p < 0.001 by one-way ANOVA. Scale bars: 50 μm (C), 25 μm (F), and 200 μm (G).

    Journal: Bioactive Materials

    Article Title: Screening of a quinonoid compounds library identifies decylubiquinone as an antioxidant and anti-apoptotic agent against glucocorticoid-induced osteoporosis via CD39/CD73/adenosine axis

    doi: 10.1016/j.bioactmat.2026.03.062

    Figure Lengend Snippet: Roles of the CD39/CD73 axis on DUB's multidirectional protection effects in Dex-treated primary BMSCs. ( A ) ELISA for ROS clearance-related enzyme T-SOD and ROS damage biomarkers 8-OHdG, AOPP, and MDA in primary BMSCs of different groups. ( B ) Western blot and quantification for the expression of ROS clearance-related proteins in primary BMSCs of different groups. ( C ) Representative images and quantitative analysis of immunofluorescence staining for MitoSox (red) in primary BMSCs of different groups, and nuclei were stained with Hoechst (blue). ( D ) Western blot and quantification for the expression of apoptosis-related proteins in primary BMSCs of different groups. ( E ) Cellular apoptosis detection in primary BMSCs of different groups by Annexin V-FITC and PI dual-staining assessment via flow cytometry. The proportion of cells in each quadrant was indicated in the plot. ( F ) Tunel (red) staining and quantification of apoptotic cells in primary BMSCs of different groups, and nuclei were stained with DAPI (blue). ( G ) Representative images and quantitative analysis of Alizarin Red S staining for mineralization in primary BMSCs of different groups under osteogenic conditions. ( H ) Western blot and quantification for the expression of osteogenesis-related proteins in primary BMSCs of different groups. n = 4 independent repeats by using different biological samples in each group for in vitro experiments. Data were means ± s.e.m. ∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗ p < 0.001 by one-way ANOVA. Scale bars: 50 μm (C), 25 μm (F), and 200 μm (G).

    Article Snippet: Additionally, apoptosis was independently assessed by using a One-step TUNEL In Situ Apoptosis Kit (E-CK-A322, Elabscience, Wuhan, China) according to the manufacturer's instructions.

    Techniques: Enzyme-linked Immunosorbent Assay, Western Blot, Expressing, Immunofluorescence, Staining, Flow Cytometry, TUNEL Assay, In Vitro

    The effect of ADO supplements on primary BMSCs. ( A ) MTT assay for the proliferation of BMSCs treated with different doses of ADO for 2 days and 10 days under osteogenic induction conditions with or without 10 μM Dex. ( B-C ) Representative images and quantitative analysis of mineralized nodule areas by Alizarin Red S staining in primary BMSCs treated with gradient doses of ADO under osteogenic induction with or without 10 μM Dex. ( D ) Western blot and quantification for the expression of osteogenesis-related proteins in primary BMSCs of different groups. ( E ) ELISA for ROS clearance-related enzyme T-SOD and ROS damage biomarkers 8-OHdG, AOPP, and MDA in primary BMSCs of different groups. ( F ) Western blot and quantification for the expression of ROS clearance-related proteins in primary BMSCs of different groups. ( G ) Representative images and quantitative analysis of immunofluorescence staining for MitoSox (red) in primary BMSCs of different groups, and nuclei were stained with Hoechst (blue). ( H ) Western blot and quantification for the expression of apoptosis-related proteins in primary BMSCs of different groups. ( I ) Cellular apoptosis detection in primary BMSCs of different groups by Annexin V-FITC and PI dual-staining assessment via flow cytometry. The proportion of cells in each quadrant was indicated in the plot. ( J ) Tunel (red) staining and quantification of apoptotic cells in primary BMSCs of different groups, and nuclei were stained with DAPI (blue). n = 4 independent repeats by using different biological samples in each group for in vitro experiments. Data were means ± s.e.m. ∗∗ p < 0.01, ∗∗∗ p < 0.001 by one-way ANOVA. Scale bars: 200 μm (B), 50 μm (G), and 25 μm (J).

    Journal: Bioactive Materials

    Article Title: Screening of a quinonoid compounds library identifies decylubiquinone as an antioxidant and anti-apoptotic agent against glucocorticoid-induced osteoporosis via CD39/CD73/adenosine axis

    doi: 10.1016/j.bioactmat.2026.03.062

    Figure Lengend Snippet: The effect of ADO supplements on primary BMSCs. ( A ) MTT assay for the proliferation of BMSCs treated with different doses of ADO for 2 days and 10 days under osteogenic induction conditions with or without 10 μM Dex. ( B-C ) Representative images and quantitative analysis of mineralized nodule areas by Alizarin Red S staining in primary BMSCs treated with gradient doses of ADO under osteogenic induction with or without 10 μM Dex. ( D ) Western blot and quantification for the expression of osteogenesis-related proteins in primary BMSCs of different groups. ( E ) ELISA for ROS clearance-related enzyme T-SOD and ROS damage biomarkers 8-OHdG, AOPP, and MDA in primary BMSCs of different groups. ( F ) Western blot and quantification for the expression of ROS clearance-related proteins in primary BMSCs of different groups. ( G ) Representative images and quantitative analysis of immunofluorescence staining for MitoSox (red) in primary BMSCs of different groups, and nuclei were stained with Hoechst (blue). ( H ) Western blot and quantification for the expression of apoptosis-related proteins in primary BMSCs of different groups. ( I ) Cellular apoptosis detection in primary BMSCs of different groups by Annexin V-FITC and PI dual-staining assessment via flow cytometry. The proportion of cells in each quadrant was indicated in the plot. ( J ) Tunel (red) staining and quantification of apoptotic cells in primary BMSCs of different groups, and nuclei were stained with DAPI (blue). n = 4 independent repeats by using different biological samples in each group for in vitro experiments. Data were means ± s.e.m. ∗∗ p < 0.01, ∗∗∗ p < 0.001 by one-way ANOVA. Scale bars: 200 μm (B), 50 μm (G), and 25 μm (J).

    Article Snippet: Additionally, apoptosis was independently assessed by using a One-step TUNEL In Situ Apoptosis Kit (E-CK-A322, Elabscience, Wuhan, China) according to the manufacturer's instructions.

    Techniques: MTT Assay, Staining, Western Blot, Expressing, Enzyme-linked Immunosorbent Assay, Immunofluorescence, Flow Cytometry, TUNEL Assay, In Vitro

    Summary of the study. The schematic diagram illustrates that DUB alleviates GIOP by suppressing oxidative stress and apoptosis via the CD39/CD73/ADO axis and promotes osteogenesis via ADO/A 2b R-mediated activation of the PKA/CREB pathway. The schematic diagram was created by using BioRender.com.

    Journal: Bioactive Materials

    Article Title: Screening of a quinonoid compounds library identifies decylubiquinone as an antioxidant and anti-apoptotic agent against glucocorticoid-induced osteoporosis via CD39/CD73/adenosine axis

    doi: 10.1016/j.bioactmat.2026.03.062

    Figure Lengend Snippet: Summary of the study. The schematic diagram illustrates that DUB alleviates GIOP by suppressing oxidative stress and apoptosis via the CD39/CD73/ADO axis and promotes osteogenesis via ADO/A 2b R-mediated activation of the PKA/CREB pathway. The schematic diagram was created by using BioRender.com.

    Article Snippet: Additionally, apoptosis was independently assessed by using a One-step TUNEL In Situ Apoptosis Kit (E-CK-A322, Elabscience, Wuhan, China) according to the manufacturer's instructions.

    Techniques: Activation Assay