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enrich sec 650 10 × 300 column  (Bio-Rad)


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    Structured Review

    Bio-Rad enrich sec 650 10 × 300 column
    Enrich Sec 650 10 × 300 Column, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/enrich+650+10+%C3%97+300+column/enrich+sec+650+10+%C3%97+300+column/pmc11372362-53-11-13
    Average 90 stars, based on 1 article reviews
    enrich sec 650 10 × 300 column - by Bioz Stars, 2026-10
    90/100 stars

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    Related Articles

    Filtration:

    Article Title: The calcium‐binding site of human glutamate carboxypeptidase II is critical for dimerization, thermal stability, and enzymatic activity
    Article Snippet: The medium was concentrated by tangential flow filtration (TFF, Millipore, Molsheim, France), dialyzed against buffer suitable for subsequent purification (50 m M Tris–HCl, 150 m M NaCl, pH 8.0) and purified by StrepTactin affinity chromatography (Strep‐Tactin Superflow, IBA, Germany) and SEC on an ENrich 650 10 × 300 column (BioRad, CA) in TBS buffer (50 m M Tris–HCl, 150 m M NaCl, pH 7.4).

    Purification:

    Article Title: The calcium‐binding site of human glutamate carboxypeptidase II is critical for dimerization, thermal stability, and enzymatic activity
    Article Snippet: The medium was concentrated by tangential flow filtration (TFF, Millipore, Molsheim, France), dialyzed against buffer suitable for subsequent purification (50 m M Tris–HCl, 150 m M NaCl, pH 8.0) and purified by StrepTactin affinity chromatography (Strep‐Tactin Superflow, IBA, Germany) and SEC on an ENrich 650 10 × 300 column (BioRad, CA) in TBS buffer (50 m M Tris–HCl, 150 m M NaCl, pH 7.4).

    Affinity Chromatography:

    Article Title: The calcium‐binding site of human glutamate carboxypeptidase II is critical for dimerization, thermal stability, and enzymatic activity
    Article Snippet: The medium was concentrated by tangential flow filtration (TFF, Millipore, Molsheim, France), dialyzed against buffer suitable for subsequent purification (50 m M Tris–HCl, 150 m M NaCl, pH 8.0) and purified by StrepTactin affinity chromatography (Strep‐Tactin Superflow, IBA, Germany) and SEC on an ENrich 650 10 × 300 column (BioRad, CA) in TBS buffer (50 m M Tris–HCl, 150 m M NaCl, pH 7.4).



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