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native imac buffer kit  (Bio-Rad)


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    Structured Review

    Bio-Rad native imac buffer kit
    <t>Purification</t> and structural characterization of His-tagged BFT variants: ( a ) Silver-stained SDS-PAGE analysis of <t>IMAC</t> purification. Lane 1: His-rNTBF culture supernatant. Lane 2: Purified and concentrated I-hBFT. Lane 3: His-rETBF culture supernatant. Lane 4: Purified and concentrated A-hBFT. Purified hBFT samples show enrichment to near homogeneity with predominant bands at ~19 kDa. ( b ) Western blot analysis of culture duration effects on His-tagged BFT expression at 24 h and 48 h for I-hBFT (lanes 1–2) and A-hBFT (lanes 3–4). ( c ) AlphaFold3-predicted structures of mature I-hBFT and A-hBFT. The E349A mutation in I-hBFT disrupts the zinc-binding motif, highlighting structural basis for catalytic inactivation. Mutated alanine residue (A349) shown in red; original glutamic acid residue (E349) shown in green.
    Native Imac Buffer Kit, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 92/100, based on 6 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/kit+buffer/Native+IMAC+Buffer+kit/pmc13120389-271-6-11
    Average 92 stars, based on 6 article reviews
    native imac buffer kit - by Bioz Stars, 2026-10
    92/100 stars

    Images

    1) Product Images from "Purification and Characterization of His-Tagged Recombinant Bacteroides fragilis Toxin-2 Variants In Vitro and In Vivo"

    Article Title: Purification and Characterization of His-Tagged Recombinant Bacteroides fragilis Toxin-2 Variants In Vitro and In Vivo

    Journal: Toxins

    doi: 10.3390/toxins18040189

    Purification and structural characterization of His-tagged BFT variants: ( a ) Silver-stained SDS-PAGE analysis of IMAC purification. Lane 1: His-rNTBF culture supernatant. Lane 2: Purified and concentrated I-hBFT. Lane 3: His-rETBF culture supernatant. Lane 4: Purified and concentrated A-hBFT. Purified hBFT samples show enrichment to near homogeneity with predominant bands at ~19 kDa. ( b ) Western blot analysis of culture duration effects on His-tagged BFT expression at 24 h and 48 h for I-hBFT (lanes 1–2) and A-hBFT (lanes 3–4). ( c ) AlphaFold3-predicted structures of mature I-hBFT and A-hBFT. The E349A mutation in I-hBFT disrupts the zinc-binding motif, highlighting structural basis for catalytic inactivation. Mutated alanine residue (A349) shown in red; original glutamic acid residue (E349) shown in green.
    Figure Legend Snippet: Purification and structural characterization of His-tagged BFT variants: ( a ) Silver-stained SDS-PAGE analysis of IMAC purification. Lane 1: His-rNTBF culture supernatant. Lane 2: Purified and concentrated I-hBFT. Lane 3: His-rETBF culture supernatant. Lane 4: Purified and concentrated A-hBFT. Purified hBFT samples show enrichment to near homogeneity with predominant bands at ~19 kDa. ( b ) Western blot analysis of culture duration effects on His-tagged BFT expression at 24 h and 48 h for I-hBFT (lanes 1–2) and A-hBFT (lanes 3–4). ( c ) AlphaFold3-predicted structures of mature I-hBFT and A-hBFT. The E349A mutation in I-hBFT disrupts the zinc-binding motif, highlighting structural basis for catalytic inactivation. Mutated alanine residue (A349) shown in red; original glutamic acid residue (E349) shown in green.

    Techniques Used: Purification, Staining, SDS Page, Western Blot, Expressing, Mutagenesis, Binding Assay, Residue

    Related Articles

    Protein Purification:

    Article Title: Anti-tumor effect of a recombinant Bifidobacterium strain secreting a claudin-targeting molecule in a mouse breast cancer model.
    Article Snippet: Bifidobacterium is a nonpathogenic strain of anaerobic bacteria that selectively localizes and proliferates in tumors.. It has emerged as a specific carrier of anticancer proteins against malignant tumors.. Claudins are tetraspanin transmembrane proteins that form tight junctions.

    Article Title: Potential Anti-Cancer Therapeutic Agents: Effects of VHH Antibodies on Mesothelin Binding Affinity in Cancer
    Article Snippet: Recombinant proteins were induced with 0.5 mM isopropyl-β-D-thiogalactopyranoside (Wako Pure Chemical Industries, Osaka, Japan). .. Protein purification was then performed using the ProfiniaTM native IMAC purification and buffer kit (Bio-Rad, CA, USA), according to the manufacturer’s instructions. .. MSLN mutant plasmids were prepared by infusion technology using an Infusion HD kit (Takara, Mie, Japan).

    Purification:

    Article Title: Anti-tumor effect of a recombinant Bifidobacterium strain secreting a claudin-targeting molecule in a mouse breast cancer model.
    Article Snippet: Bifidobacterium is a nonpathogenic strain of anaerobic bacteria that selectively localizes and proliferates in tumors.. It has emerged as a specific carrier of anticancer proteins against malignant tumors.. Claudins are tetraspanin transmembrane proteins that form tight junctions.

    Article Title: HCV NS3 recombinant antigens and mutants thereof for improved antibody detection
    Article Snippet: .. IMAC purification was performed on the lysate soluble fraction using the Native IMAC Buffer Kit and Profinity IMAC cartridge (BioRad) according to the manufacture's protocol. ..

    Article Title: Purification and Characterization of His-Tagged Recombinant Bacteroides fragilis Toxin-2 Variants In Vitro and In Vivo.
    Article Snippet: .. Alternative purification was performed using the Native IMAC Buffer Kit (#6200239, Bio-Rad, Hercules, CA, USA) with gravityflow glass columns. ..

    Article Title: HCV antigen-antibody combination assay and methods and compositions for use therein
    Article Snippet: .. IMAC purification was performed on the lysate soluble fraction using the Native IMAC Buffer Kit and Profinity IMAC cartridge (BioRad) according to the manufacture's protocol. ..

    Article Title: Engineering of the hepatitis C virus helicase for enhanced seroreactivity.
    Article Snippet: Accepted Manuscript Title: Engineering of the Hepatitis C Virus Helicase for Enhanced Seroreactivity Authors: Christopher C. Marohnic, Larry G. Birkenmeyer, M. Felicia Bogdan, Edwin C. Frias, Kathy S. Otis, Mary Ann P. Palafox, Troy D. McSherry, Svetoslava D. Gregory, Cheng Zhao, Robin A. Gutierrez, John C. Prostko, A. Scott Muerhoff PII: S0166-0934(18)30398-7 DOI: https://doi.org/10.1016/j.jviromet.2018.10.019 Reference: VIRMET 13560 To appear in: Journal of Virological Methods Received date: 7-8-2018 Revised date: 24-10-2018 Accepted date: 25-10-2018 Please cite this article as: Marohnic CC, Birkenmeyer LG, Bogdan MF, Frias EC, Otis KS, Palafox MAP, McSherry TD, Gregory SD, Zhao C, Gutierrez RA, Prostko JC, Muerhoff AS, Engineering of the Hepatitis C Virus Helicase for Enhanced Seroreactivity, Journal of Virological Methods (2018), https://doi.org/10.1016/j.jviromet.2018.10.019 This is a PDF file of an unedited manuscript that has been accepted for publication.. As a service to our customers we are providing this early version of the manuscript.. The manuscript will undergo copyediting, typesetting, and review of the resulting proof before it is published in its final form.

    Article Title: Purification and Characterization of His-Tagged Recombinant Bacteroides fragilis Toxin-2 Variants In Vitro and In Vivo
    Article Snippet: .. Alternative purification was performed using the Native IMAC Buffer Kit (#6200239, Bio-Rad, Hercules, CA, USA) with gravity-flow glass columns. ..

    Article Title: Recombinant production of Morus alba lipid transfer protein and prediction of its allergenic epitopes
    Article Snippet: Background.. – White mulberry (Morus alba) pollen grains trigger allergic diseases including asthma, allergic rhinitis, and allergic conjunctivitis.. Non-specific lipid transfer proteins (nsLTPs) are robust allergens found in higher plants.

    Article Title: Potential Anti-Cancer Therapeutic Agents: Effects of VHH Antibodies on Mesothelin Binding Affinity in Cancer
    Article Snippet: Recombinant proteins were induced with 0.5 mM isopropyl-β-D-thiogalactopyranoside (Wako Pure Chemical Industries, Osaka, Japan). .. Protein purification was then performed using the ProfiniaTM native IMAC purification and buffer kit (Bio-Rad, CA, USA), according to the manufacturer’s instructions. .. MSLN mutant plasmids were prepared by infusion technology using an Infusion HD kit (Takara, Mie, Japan).



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