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human recombinant glo  (R&D Systems)


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    Structured Review

    R&D Systems human recombinant glo
    The crystal structure of <t>human</t> <t>Glo-I</t> (PDB code 3W0T). ( a ) Schematic representation of the human Glo-I structures (PDB code 3W0T) in cartoon representation, the ligand is shown in balls and sticks and Zn + 2 ions as CPK style gray spheres. ( b ) Surface representation of the human Glo-I structure showing the location of the binding sites at the interface of the two homodimers.
    Human Recombinant Glo, supplied by R&D Systems, used in various techniques. Bioz Stars score: 94/100, based on 23 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/human recombinant glo/product/R&D Systems
    Average 94 stars, based on 23 article reviews
    human recombinant glo - by Bioz Stars, 2026-06
    94/100 stars

    Images

    1) Product Images from "Discovery of hydroxytriazole as a potential glyoxalase-I inhibitor utilizing computer-aided drug design techniques"

    Article Title: Discovery of hydroxytriazole as a potential glyoxalase-I inhibitor utilizing computer-aided drug design techniques

    Journal: Scientific Reports

    doi: 10.1038/s41598-026-40497-4

    The crystal structure of human Glo-I (PDB code 3W0T). ( a ) Schematic representation of the human Glo-I structures (PDB code 3W0T) in cartoon representation, the ligand is shown in balls and sticks and Zn + 2 ions as CPK style gray spheres. ( b ) Surface representation of the human Glo-I structure showing the location of the binding sites at the interface of the two homodimers.
    Figure Legend Snippet: The crystal structure of human Glo-I (PDB code 3W0T). ( a ) Schematic representation of the human Glo-I structures (PDB code 3W0T) in cartoon representation, the ligand is shown in balls and sticks and Zn + 2 ions as CPK style gray spheres. ( b ) Surface representation of the human Glo-I structure showing the location of the binding sites at the interface of the two homodimers.

    Techniques Used: Binding Assay

    Schematic representation of the 96-well plate setup for the Glo-I bioassay, used to assess enzyme activity across various test samples.
    Figure Legend Snippet: Schematic representation of the 96-well plate setup for the Glo-I bioassay, used to assess enzyme activity across various test samples.

    Techniques Used: Bioassay, Activity Assay

    ( a ) 3D view of ( HTS06312SC ) in Glo-I active site. ( b ) 2D interactions between ( HTS06312SC ) and Glo-I active site.
    Figure Legend Snippet: ( a ) 3D view of ( HTS06312SC ) in Glo-I active site. ( b ) 2D interactions between ( HTS06312SC ) and Glo-I active site.

    Techniques Used:

    ( a ) 3D view of ( BTB02024SC ) in Glo-I active site. ( b ) 2D interactions between ( BTB02024SC ) and Glo-I.
    Figure Legend Snippet: ( a ) 3D view of ( BTB02024SC ) in Glo-I active site. ( b ) 2D interactions between ( BTB02024SC ) and Glo-I.

    Techniques Used:

    ( a ) 3D view of ( SPB07393SC ) in Glo-I active site. ( b ) 2D interactions between ( SPB07393SC ) and Glo-I.
    Figure Legend Snippet: ( a ) 3D view of ( SPB07393SC ) in Glo-I active site. ( b ) 2D interactions between ( SPB07393SC ) and Glo-I.

    Techniques Used:

    Structural dynamics of Glo-I RMSD ( a ), ligands RMSD ( b ), Glo-I radius of gyration ( c ), and SASA values ( d ) calculated during the 100 ns of MD trajectories.
    Figure Legend Snippet: Structural dynamics of Glo-I RMSD ( a ), ligands RMSD ( b ), Glo-I radius of gyration ( c ), and SASA values ( d ) calculated during the 100 ns of MD trajectories.

    Techniques Used:

    Graph showing the inhibitory activity of selected compounds (1–16) against Glo-I and their corresponding IC50 values.
    Figure Legend Snippet: Graph showing the inhibitory activity of selected compounds (1–16) against Glo-I and their corresponding IC50 values.

    Techniques Used: Activity Assay



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    The crystal structure of <t>human</t> <t>Glo-I</t> (PDB code 3W0T). ( a ) Schematic representation of the human Glo-I structures (PDB code 3W0T) in cartoon representation, the ligand is shown in balls and sticks and Zn + 2 ions as CPK style gray spheres. ( b ) Surface representation of the human Glo-I structure showing the location of the binding sites at the interface of the two homodimers.
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    The crystal structure of <t>human</t> <t>Glo-I</t> (PDB code 3W0T). ( a ) Schematic representation of the human Glo-I structures (PDB code 3W0T) in cartoon representation, the ligand is shown in balls and sticks and Zn + 2 ions as CPK style gray spheres. ( b ) Surface representation of the human Glo-I structure showing the location of the binding sites at the interface of the two homodimers.
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    The crystal structure of <t>human</t> <t>Glo-I</t> (PDB code 3W0T). ( a ) Schematic representation of the human Glo-I structures (PDB code 3W0T) in cartoon representation, the ligand is shown in balls and sticks and Zn + 2 ions as CPK style gray spheres. ( b ) Surface representation of the human Glo-I structure showing the location of the binding sites at the interface of the two homodimers.
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    R&D Systems vitro against recombinant human glo
    The crystal structure of <t>human</t> <t>Glo-I</t> (PDB code 3W0T). ( a ) Schematic representation of the human Glo-I structures (PDB code 3W0T) in cartoon representation, the ligand is shown in balls and sticks and Zn + 2 ions as CPK style gray spheres. ( b ) Surface representation of the human Glo-I structure showing the location of the binding sites at the interface of the two homodimers.
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    The crystal structure of <t>human</t> <t>Glo-I</t> (PDB code 3W0T). ( a ) Schematic representation of the human Glo-I structures (PDB code 3W0T) in cartoon representation, the ligand is shown in balls and sticks and Zn + 2 ions as CPK style gray spheres. ( b ) Surface representation of the human Glo-I structure showing the location of the binding sites at the interface of the two homodimers.
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    The crystal structure of <t>human</t> <t>Glo-I</t> (PDB code 3W0T). ( a ) Schematic representation of the human Glo-I structures (PDB code 3W0T) in cartoon representation, the ligand is shown in balls and sticks and Zn + 2 ions as CPK style gray spheres. ( b ) Surface representation of the human Glo-I structure showing the location of the binding sites at the interface of the two homodimers.
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    Image Search Results


    The crystal structure of human Glo-I (PDB code 3W0T). ( a ) Schematic representation of the human Glo-I structures (PDB code 3W0T) in cartoon representation, the ligand is shown in balls and sticks and Zn + 2 ions as CPK style gray spheres. ( b ) Surface representation of the human Glo-I structure showing the location of the binding sites at the interface of the two homodimers.

    Journal: Scientific Reports

    Article Title: Discovery of hydroxytriazole as a potential glyoxalase-I inhibitor utilizing computer-aided drug design techniques

    doi: 10.1038/s41598-026-40497-4

    Figure Lengend Snippet: The crystal structure of human Glo-I (PDB code 3W0T). ( a ) Schematic representation of the human Glo-I structures (PDB code 3W0T) in cartoon representation, the ligand is shown in balls and sticks and Zn + 2 ions as CPK style gray spheres. ( b ) Surface representation of the human Glo-I structure showing the location of the binding sites at the interface of the two homodimers.

    Article Snippet: Experimental materials included human recombinant GLO-I (rhGLO-I) and coli-derived Ala2-Met184 with an N-terminal Met and 6-His tag (R&D Systems Corporation, USA) to test the inhibitory activity of the chosen compounds against GLO-I in vitro.

    Techniques: Binding Assay

    Schematic representation of the 96-well plate setup for the Glo-I bioassay, used to assess enzyme activity across various test samples.

    Journal: Scientific Reports

    Article Title: Discovery of hydroxytriazole as a potential glyoxalase-I inhibitor utilizing computer-aided drug design techniques

    doi: 10.1038/s41598-026-40497-4

    Figure Lengend Snippet: Schematic representation of the 96-well plate setup for the Glo-I bioassay, used to assess enzyme activity across various test samples.

    Article Snippet: Experimental materials included human recombinant GLO-I (rhGLO-I) and coli-derived Ala2-Met184 with an N-terminal Met and 6-His tag (R&D Systems Corporation, USA) to test the inhibitory activity of the chosen compounds against GLO-I in vitro.

    Techniques: Bioassay, Activity Assay

    ( a ) 3D view of ( HTS06312SC ) in Glo-I active site. ( b ) 2D interactions between ( HTS06312SC ) and Glo-I active site.

    Journal: Scientific Reports

    Article Title: Discovery of hydroxytriazole as a potential glyoxalase-I inhibitor utilizing computer-aided drug design techniques

    doi: 10.1038/s41598-026-40497-4

    Figure Lengend Snippet: ( a ) 3D view of ( HTS06312SC ) in Glo-I active site. ( b ) 2D interactions between ( HTS06312SC ) and Glo-I active site.

    Article Snippet: Experimental materials included human recombinant GLO-I (rhGLO-I) and coli-derived Ala2-Met184 with an N-terminal Met and 6-His tag (R&D Systems Corporation, USA) to test the inhibitory activity of the chosen compounds against GLO-I in vitro.

    Techniques:

    ( a ) 3D view of ( BTB02024SC ) in Glo-I active site. ( b ) 2D interactions between ( BTB02024SC ) and Glo-I.

    Journal: Scientific Reports

    Article Title: Discovery of hydroxytriazole as a potential glyoxalase-I inhibitor utilizing computer-aided drug design techniques

    doi: 10.1038/s41598-026-40497-4

    Figure Lengend Snippet: ( a ) 3D view of ( BTB02024SC ) in Glo-I active site. ( b ) 2D interactions between ( BTB02024SC ) and Glo-I.

    Article Snippet: Experimental materials included human recombinant GLO-I (rhGLO-I) and coli-derived Ala2-Met184 with an N-terminal Met and 6-His tag (R&D Systems Corporation, USA) to test the inhibitory activity of the chosen compounds against GLO-I in vitro.

    Techniques:

    ( a ) 3D view of ( SPB07393SC ) in Glo-I active site. ( b ) 2D interactions between ( SPB07393SC ) and Glo-I.

    Journal: Scientific Reports

    Article Title: Discovery of hydroxytriazole as a potential glyoxalase-I inhibitor utilizing computer-aided drug design techniques

    doi: 10.1038/s41598-026-40497-4

    Figure Lengend Snippet: ( a ) 3D view of ( SPB07393SC ) in Glo-I active site. ( b ) 2D interactions between ( SPB07393SC ) and Glo-I.

    Article Snippet: Experimental materials included human recombinant GLO-I (rhGLO-I) and coli-derived Ala2-Met184 with an N-terminal Met and 6-His tag (R&D Systems Corporation, USA) to test the inhibitory activity of the chosen compounds against GLO-I in vitro.

    Techniques:

    Structural dynamics of Glo-I RMSD ( a ), ligands RMSD ( b ), Glo-I radius of gyration ( c ), and SASA values ( d ) calculated during the 100 ns of MD trajectories.

    Journal: Scientific Reports

    Article Title: Discovery of hydroxytriazole as a potential glyoxalase-I inhibitor utilizing computer-aided drug design techniques

    doi: 10.1038/s41598-026-40497-4

    Figure Lengend Snippet: Structural dynamics of Glo-I RMSD ( a ), ligands RMSD ( b ), Glo-I radius of gyration ( c ), and SASA values ( d ) calculated during the 100 ns of MD trajectories.

    Article Snippet: Experimental materials included human recombinant GLO-I (rhGLO-I) and coli-derived Ala2-Met184 with an N-terminal Met and 6-His tag (R&D Systems Corporation, USA) to test the inhibitory activity of the chosen compounds against GLO-I in vitro.

    Techniques:

    Graph showing the inhibitory activity of selected compounds (1–16) against Glo-I and their corresponding IC50 values.

    Journal: Scientific Reports

    Article Title: Discovery of hydroxytriazole as a potential glyoxalase-I inhibitor utilizing computer-aided drug design techniques

    doi: 10.1038/s41598-026-40497-4

    Figure Lengend Snippet: Graph showing the inhibitory activity of selected compounds (1–16) against Glo-I and their corresponding IC50 values.

    Article Snippet: Experimental materials included human recombinant GLO-I (rhGLO-I) and coli-derived Ala2-Met184 with an N-terminal Met and 6-His tag (R&D Systems Corporation, USA) to test the inhibitory activity of the chosen compounds against GLO-I in vitro.

    Techniques: Activity Assay