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profinity exact tm  (Bio-Rad)


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    Bio-Rad profinity exact tm
    The purity of recombinant annexin V was analyzed by 15% (w/v) SDS-PAGE. M, molecular weight maker; Whole cells, whole proteins of the cell lysate; DEAE, annexin V protein after DEAE chromatography; <t>Profinity</t> <t>eXact,</t> annexin V protein after Profinity eXact purification. A band of ≈50 kDa was observed as a main band after DEAE chromatography, but after the tag was removed during elution procedure, a band consistent with the molecular weight of annexin V (36 kDa) was detected. The band position of annexin V after Profinity eXact purification was indicated by the arrow.
    Profinity Exact Tm, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 93/100, based on 38 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/profinity exact tm/product/Bio-Rad
    Average 93 stars, based on 38 article reviews
    profinity exact tm - by Bioz Stars, 2026-05
    93/100 stars

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    1) Product Images from "Importance of annexin V N-terminus for 2D crystal formation and quick purification protocol of recombinant annexin V"

    Article Title: Importance of annexin V N-terminus for 2D crystal formation and quick purification protocol of recombinant annexin V

    Journal: PLOS ONE

    doi: 10.1371/journal.pone.0278553

    The purity of recombinant annexin V was analyzed by 15% (w/v) SDS-PAGE. M, molecular weight maker; Whole cells, whole proteins of the cell lysate; DEAE, annexin V protein after DEAE chromatography; Profinity eXact, annexin V protein after Profinity eXact purification. A band of ≈50 kDa was observed as a main band after DEAE chromatography, but after the tag was removed during elution procedure, a band consistent with the molecular weight of annexin V (36 kDa) was detected. The band position of annexin V after Profinity eXact purification was indicated by the arrow.
    Figure Legend Snippet: The purity of recombinant annexin V was analyzed by 15% (w/v) SDS-PAGE. M, molecular weight maker; Whole cells, whole proteins of the cell lysate; DEAE, annexin V protein after DEAE chromatography; Profinity eXact, annexin V protein after Profinity eXact purification. A band of ≈50 kDa was observed as a main band after DEAE chromatography, but after the tag was removed during elution procedure, a band consistent with the molecular weight of annexin V (36 kDa) was detected. The band position of annexin V after Profinity eXact purification was indicated by the arrow.

    Techniques Used: Recombinant, SDS Page, Molecular Weight, Chromatography, Purification



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    Image Search Results


    The purity of recombinant annexin V was analyzed by 15% (w/v) SDS-PAGE. M, molecular weight maker; Whole cells, whole proteins of the cell lysate; DEAE, annexin V protein after DEAE chromatography; Profinity eXact, annexin V protein after Profinity eXact purification. A band of ≈50 kDa was observed as a main band after DEAE chromatography, but after the tag was removed during elution procedure, a band consistent with the molecular weight of annexin V (36 kDa) was detected. The band position of annexin V after Profinity eXact purification was indicated by the arrow.

    Journal: PLOS ONE

    Article Title: Importance of annexin V N-terminus for 2D crystal formation and quick purification protocol of recombinant annexin V

    doi: 10.1371/journal.pone.0278553

    Figure Lengend Snippet: The purity of recombinant annexin V was analyzed by 15% (w/v) SDS-PAGE. M, molecular weight maker; Whole cells, whole proteins of the cell lysate; DEAE, annexin V protein after DEAE chromatography; Profinity eXact, annexin V protein after Profinity eXact purification. A band of ≈50 kDa was observed as a main band after DEAE chromatography, but after the tag was removed during elution procedure, a band consistent with the molecular weight of annexin V (36 kDa) was detected. The band position of annexin V after Profinity eXact purification was indicated by the arrow.

    Article Snippet: The column was washed with 10 column volume of the same buffer, and the flow through fraction containing annexin V was applied to a Profinity eXact TM (exact affinity cleavage technology, Bio-rad, CA, US) protein purification column equilibrated with 100 mM NaPi (pH 7.2) in cold room (4°C).

    Techniques: Recombinant, SDS Page, Molecular Weight, Chromatography, Purification