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buffer  (Bio-Rad)


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  • 96

    Structured Review

    Bio-Rad buffer
    Buffer, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 96/100, based on 3636 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/gel+filtration+buffer/Gel+Filtration+Standard/pmc13170773-113-132-138
    Average 96 stars, based on 3636 article reviews
    buffer - by Bioz Stars, 2026-10
    96/100 stars

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    Related Articles

    Purification:

    Article Title: Isolation of ClpB & DnaK bi-chaperones from obligate pathogen <em>Anaplasma phagocytophilum</em> as future therapeutic targets
    Article Snippet: .. The concentrated Anaplasma ClpB or DnaK were further purified by gel filtration chromatography on a Superdex 200 column (Bio-Rad) equilibrated with gel filtration buffer (50 mM Tris-HCl, pH 7.5, 0.2 M KCl, 20 mM MgCl2, 10% glycerol, 1 mM EDTA, 1 mM DTT). ..

    Article Title: Structural and Antiviral Studies of the Human Norovirus GII.4 Protease
    Article Snippet: .. Purified Minerva C139A protease was buffer exchanged from gel filtration buffer to 20 mM MES pH 6 using Micro Bio Spin Chromatography Columns (Bio Rad) and subsequently concentrated using Ultrafree-MC concentrators (Millipore, 10kD) to 20 mg/mL. ..

    Article Title: Mechanism of the Multistep Catalytic Cycle of 6-Hydroxynicotinate 3-Monooxygenase Revealed by Global Kinetic Analysis.
    Article Snippet: The class A flavoenzyme 6-hydroxynicotinate 3-monooxygenase (NicC) catalyzes a rare decarboxylative hydroxylation reaction in the degradation of nicotinate by aerobic bacteria.. While the structure and critical residues involved in catalysis have been reported, the mechanism of this multistep enzyme has yet to be determined.. A kinetic understanding of the NicC mechanism would enable comparison to other phenolic hydroxylases and illuminate its bioengineering potential for remediation of N-heterocyclic aromatic compounds.

    Filtration:

    Article Title: Isolation of ClpB & DnaK bi-chaperones from obligate pathogen <em>Anaplasma phagocytophilum</em> as future therapeutic targets
    Article Snippet: .. The concentrated Anaplasma ClpB or DnaK were further purified by gel filtration chromatography on a Superdex 200 column (Bio-Rad) equilibrated with gel filtration buffer (50 mM Tris-HCl, pH 7.5, 0.2 M KCl, 20 mM MgCl2, 10% glycerol, 1 mM EDTA, 1 mM DTT). ..

    Article Title: Structural and Antiviral Studies of the Human Norovirus GII.4 Protease
    Article Snippet: .. Purified Minerva C139A protease was buffer exchanged from gel filtration buffer to 20 mM MES pH 6 using Micro Bio Spin Chromatography Columns (Bio Rad) and subsequently concentrated using Ultrafree-MC concentrators (Millipore, 10kD) to 20 mg/mL. ..

    Article Title: Probing the Cancer Mutational Landscape of <scp>KMT2</scp> Regulatory Subunits
    Article Snippet: RbBP5WBM peptides were purchased from Genscript USA Inc. .. A mixture of 7.5X SYPRO Orange (Invitrogen), ASH2LSPRY WT or mutants (30 μM) was preequilibrated in the gel filtration buffer by incubating on ice for 20 min. A melting curve protocol was run on a BioRad CFX96 Touch Real- Time PCR machine, with temperatures ranging from 10°C to 95°C at a heating rate of 0.5°C per cycle, each lasting 1 s. Data were analyzed using CFX Maestro Software, and the second derivative of the fluorescence 15306860, 2026, 7, D ow nloaded from https://faseb.onlinelibrary.w iley.com /doi/10.1096/fj.202504644R , W iley O nline L ibrary on [10/04/2026]. ..

    Article Title: Functional interactions of Gp22 and Gp23 with Gp21 DNA helicase define the replication module of dairy-relevant Ceduovirus phage 94p4.
    Article Snippet: Size exclusion chromatography (SEC) of purified Gp21, Gp22 and Gp23 proteins was performed using the ÄKTA Purifier system (GE Healthcare, Chicago, IL, USA) equipped with a Superdex 200 10/300 column (Sigma-Aldrich, St. Louis, MO, USA). .. The column was equilibrated with gel filtration buffer (50 mM Tris-HCl pH 8.0, 300 mM NaCl) and calibrated with molecular mass standards (BioRad, Warsaw, Poland): thyroglobulin (670 kDa), γ-globulin (158 kDa), ovalbumin (44 kDa), myoglobin (17 kDa), and vitamin B12 (1.35 kDa). ..

    Article Title: Structural and Antiviral Studies of the Human Norovirus GII.4 Protease
    Article Snippet: .. The protein buffer was exchanged from gel filtration buffer (20 mM Tris pH 7.5, 150 mM NaCl, 5% glycerol) to optimized GII.4 protease buffer (20 mM MES pH6.0) with Micro Bio Spin Chromatography Column (Bio Rad). ..

    Article Title: Mechanism of the Multistep Catalytic Cycle of 6-Hydroxynicotinate 3-Monooxygenase Revealed by Global Kinetic Analysis.
    Article Snippet: The class A flavoenzyme 6-hydroxynicotinate 3-monooxygenase (NicC) catalyzes a rare decarboxylative hydroxylation reaction in the degradation of nicotinate by aerobic bacteria.. While the structure and critical residues involved in catalysis have been reported, the mechanism of this multistep enzyme has yet to be determined.. A kinetic understanding of the NicC mechanism would enable comparison to other phenolic hydroxylases and illuminate its bioengineering potential for remediation of N-heterocyclic aromatic compounds.

    Article Title: Probing the Cancer Mutational Landscape of KMT2 Regulatory Subunits
    Article Snippet: RbBP5 WBM peptides were purchased from Genscript USA Inc. .. A mixture of 7.5X SYPRO Orange (Invitrogen), ASH2L SPRY WT or mutants (30 μM) was preequilibrated in the gel filtration buffer by incubating on ice for 20 min. A melting curve protocol was run on a BioRad CFX96 Touch Real‐Time PCR machine, with temperatures ranging from 10°C to 95°C at a heating rate of 0.5°C per cycle, each lasting 1 s. Data were analyzed using CFX Maestro Software, and the second derivative of the fluorescence signal was used to determine the melting temperature (T m ). ..

    Chromatography:

    Article Title: Isolation of ClpB &amp;amp; DnaK bi-chaperones from obligate pathogen &lt;em&gt;Anaplasma phagocytophilum&lt;/em&gt; as future therapeutic targets
    Article Snippet: .. The concentrated Anaplasma ClpB or DnaK were further purified by gel filtration chromatography on a Superdex 200 column (Bio-Rad) equilibrated with gel filtration buffer (50 mM Tris-HCl, pH 7.5, 0.2 M KCl, 20 mM MgCl2, 10% glycerol, 1 mM EDTA, 1 mM DTT). ..

    Article Title: Structural and Antiviral Studies of the Human Norovirus GII.4 Protease
    Article Snippet: .. Purified Minerva C139A protease was buffer exchanged from gel filtration buffer to 20 mM MES pH 6 using Micro Bio Spin Chromatography Columns (Bio Rad) and subsequently concentrated using Ultrafree-MC concentrators (Millipore, 10kD) to 20 mg/mL. ..

    Article Title: Structural and Antiviral Studies of the Human Norovirus GII.4 Protease
    Article Snippet: .. The protein buffer was exchanged from gel filtration buffer (20 mM Tris pH 7.5, 150 mM NaCl, 5% glycerol) to optimized GII.4 protease buffer (20 mM MES pH6.0) with Micro Bio Spin Chromatography Column (Bio Rad). ..

    Real-time Polymerase Chain Reaction:

    Article Title: Probing the Cancer Mutational Landscape of <scp>KMT2</scp> Regulatory Subunits
    Article Snippet: RbBP5WBM peptides were purchased from Genscript USA Inc. .. A mixture of 7.5X SYPRO Orange (Invitrogen), ASH2LSPRY WT or mutants (30 μM) was preequilibrated in the gel filtration buffer by incubating on ice for 20 min. A melting curve protocol was run on a BioRad CFX96 Touch Real- Time PCR machine, with temperatures ranging from 10°C to 95°C at a heating rate of 0.5°C per cycle, each lasting 1 s. Data were analyzed using CFX Maestro Software, and the second derivative of the fluorescence 15306860, 2026, 7, D ow nloaded from https://faseb.onlinelibrary.w iley.com /doi/10.1096/fj.202504644R , W iley O nline L ibrary on [10/04/2026]. ..

    Article Title: Probing the Cancer Mutational Landscape of KMT2 Regulatory Subunits
    Article Snippet: RbBP5 WBM peptides were purchased from Genscript USA Inc. .. A mixture of 7.5X SYPRO Orange (Invitrogen), ASH2L SPRY WT or mutants (30 μM) was preequilibrated in the gel filtration buffer by incubating on ice for 20 min. A melting curve protocol was run on a BioRad CFX96 Touch Real‐Time PCR machine, with temperatures ranging from 10°C to 95°C at a heating rate of 0.5°C per cycle, each lasting 1 s. Data were analyzed using CFX Maestro Software, and the second derivative of the fluorescence signal was used to determine the melting temperature (T m ). ..

    Maestro Software:

    Article Title: Probing the Cancer Mutational Landscape of <scp>KMT2</scp> Regulatory Subunits
    Article Snippet: RbBP5WBM peptides were purchased from Genscript USA Inc. .. A mixture of 7.5X SYPRO Orange (Invitrogen), ASH2LSPRY WT or mutants (30 μM) was preequilibrated in the gel filtration buffer by incubating on ice for 20 min. A melting curve protocol was run on a BioRad CFX96 Touch Real- Time PCR machine, with temperatures ranging from 10°C to 95°C at a heating rate of 0.5°C per cycle, each lasting 1 s. Data were analyzed using CFX Maestro Software, and the second derivative of the fluorescence 15306860, 2026, 7, D ow nloaded from https://faseb.onlinelibrary.w iley.com /doi/10.1096/fj.202504644R , W iley O nline L ibrary on [10/04/2026]. ..

    Article Title: Probing the Cancer Mutational Landscape of KMT2 Regulatory Subunits
    Article Snippet: RbBP5 WBM peptides were purchased from Genscript USA Inc. .. A mixture of 7.5X SYPRO Orange (Invitrogen), ASH2L SPRY WT or mutants (30 μM) was preequilibrated in the gel filtration buffer by incubating on ice for 20 min. A melting curve protocol was run on a BioRad CFX96 Touch Real‐Time PCR machine, with temperatures ranging from 10°C to 95°C at a heating rate of 0.5°C per cycle, each lasting 1 s. Data were analyzed using CFX Maestro Software, and the second derivative of the fluorescence signal was used to determine the melting temperature (T m ). ..

    Fluorescence:

    Article Title: Probing the Cancer Mutational Landscape of <scp>KMT2</scp> Regulatory Subunits
    Article Snippet: RbBP5WBM peptides were purchased from Genscript USA Inc. .. A mixture of 7.5X SYPRO Orange (Invitrogen), ASH2LSPRY WT or mutants (30 μM) was preequilibrated in the gel filtration buffer by incubating on ice for 20 min. A melting curve protocol was run on a BioRad CFX96 Touch Real- Time PCR machine, with temperatures ranging from 10°C to 95°C at a heating rate of 0.5°C per cycle, each lasting 1 s. Data were analyzed using CFX Maestro Software, and the second derivative of the fluorescence 15306860, 2026, 7, D ow nloaded from https://faseb.onlinelibrary.w iley.com /doi/10.1096/fj.202504644R , W iley O nline L ibrary on [10/04/2026]. ..

    Article Title: Probing the Cancer Mutational Landscape of KMT2 Regulatory Subunits
    Article Snippet: RbBP5 WBM peptides were purchased from Genscript USA Inc. .. A mixture of 7.5X SYPRO Orange (Invitrogen), ASH2L SPRY WT or mutants (30 μM) was preequilibrated in the gel filtration buffer by incubating on ice for 20 min. A melting curve protocol was run on a BioRad CFX96 Touch Real‐Time PCR machine, with temperatures ranging from 10°C to 95°C at a heating rate of 0.5°C per cycle, each lasting 1 s. Data were analyzed using CFX Maestro Software, and the second derivative of the fluorescence signal was used to determine the melting temperature (T m ). ..

    Cloning:

    Article Title: Mechanism of the Multistep Catalytic Cycle of 6-Hydroxynicotinate 3-Monooxygenase Revealed by Global Kinetic Analysis.
    Article Snippet: The class A flavoenzyme 6-hydroxynicotinate 3-monooxygenase (NicC) catalyzes a rare decarboxylative hydroxylation reaction in the degradation of nicotinate by aerobic bacteria.. While the structure and critical residues involved in catalysis have been reported, the mechanism of this multistep enzyme has yet to be determined.. A kinetic understanding of the NicC mechanism would enable comparison to other phenolic hydroxylases and illuminate its bioengineering potential for remediation of N-heterocyclic aromatic compounds.

    Expressing:

    Article Title: Mechanism of the Multistep Catalytic Cycle of 6-Hydroxynicotinate 3-Monooxygenase Revealed by Global Kinetic Analysis.
    Article Snippet: The class A flavoenzyme 6-hydroxynicotinate 3-monooxygenase (NicC) catalyzes a rare decarboxylative hydroxylation reaction in the degradation of nicotinate by aerobic bacteria.. While the structure and critical residues involved in catalysis have been reported, the mechanism of this multistep enzyme has yet to be determined.. A kinetic understanding of the NicC mechanism would enable comparison to other phenolic hydroxylases and illuminate its bioengineering potential for remediation of N-heterocyclic aromatic compounds.

    Plasmid Preparation:

    Article Title: Mechanism of the Multistep Catalytic Cycle of 6-Hydroxynicotinate 3-Monooxygenase Revealed by Global Kinetic Analysis.
    Article Snippet: The class A flavoenzyme 6-hydroxynicotinate 3-monooxygenase (NicC) catalyzes a rare decarboxylative hydroxylation reaction in the degradation of nicotinate by aerobic bacteria.. While the structure and critical residues involved in catalysis have been reported, the mechanism of this multistep enzyme has yet to be determined.. A kinetic understanding of the NicC mechanism would enable comparison to other phenolic hydroxylases and illuminate its bioengineering potential for remediation of N-heterocyclic aromatic compounds.

    Recombinant:

    Article Title: Mechanism of the Multistep Catalytic Cycle of 6-Hydroxynicotinate 3-Monooxygenase Revealed by Global Kinetic Analysis.
    Article Snippet: The class A flavoenzyme 6-hydroxynicotinate 3-monooxygenase (NicC) catalyzes a rare decarboxylative hydroxylation reaction in the degradation of nicotinate by aerobic bacteria.. While the structure and critical residues involved in catalysis have been reported, the mechanism of this multistep enzyme has yet to be determined.. A kinetic understanding of the NicC mechanism would enable comparison to other phenolic hydroxylases and illuminate its bioengineering potential for remediation of N-heterocyclic aromatic compounds.



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