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mini whole gel eluter  (Bio-Rad)


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    Structured Review

    Bio-Rad mini whole gel eluter
    Mini Whole Gel Eluter, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 93/100, based on 68 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/whole+gel+eluter/Mini+Whole+Gel+Eluter+Template/pm39370076-68-9-13
    Average 93 stars, based on 68 article reviews
    mini whole gel eluter - by Bioz Stars, 2026-10
    93/100 stars

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    Related Articles

    Purification:

    Article Title: Actinobacillus pleuropneumoniae encodes multiple phase-variable DNA methyltransferases that control distinct phasevarions
    Article Snippet: .. TRD-less Mod proteins for both ModP and ModQ were then further purified by electroelution (100 mA for 30 min) into 1× MOPS buffer using a mini whole gel eluter (Biorad, Gladesville, NSW, Australia). .. Protein fractions were collected from each well and analysed by silver staining (Sigma) and Western blot using monoclonal anti poly histidine alkaline phosphatase antibody (1:20 000 dilution).

    Article Title: Actinobacillus pleuropneumoniae encodes multiple phase-variable DNA methyltransferases that comprise distinct phasevarions
    Article Snippet: .. TRD-less Mod proteins for both ModP and ModQ were then further purified by electroelution (100 mA for 30 min) into 1x MOPS buffer using a mini whole gel eluter (Biorad, Gladesville, NSW, Australia). .. Protein fractions were collected from each well and analysed by silver staining (Sigma) and Western blot using monoclonal anti poly histidine alkaline phosphatase antibody (1:20,000 dilution).

    Article Title: Actinobacillus pleuropneumoniae encodes multiple phase-variable DNA methyltransferases that control distinct phasevarions.
    Article Snippet: .. TRD-less Mod proteins for both ModP and ModQ were then further purified by electroelution (100 mA for 30 min) into 1× MOPS buffer using a mini whole gel eluter (Biorad, Gladesville, NSW, Australia). .. Protein fractions were collected from each well and analysed by silver staining (Sigma) and Western blot using monoclonal anti poly histidine alkaline phosphatase antibody (1:20 000 dilution).

    Nucleic Acid Electrophoresis:

    Article Title: Intact proteome fractionation strategies compatible with mass spectrometry.
    Article Snippet: www.expert-reviews.com ISSN 1478-9450 © 2011 Expert Reviews Ltd 10.1586/EPR.11.67 Within its approximately 20-year history, proteome analysis has been aided primarily through instrumental advances.. Relative to the instrumentation used in the first peptide mass fingerprinting and peptide sequencing experiments, today’s mass spectrometers scan faster, and are more sensitive, selective and versatile than ever before.. Sparked by the development of soft ionization (i.e., MALDI, ESI), biological mass spectrometry (MS) has evolved through novel fragmentation strategies (electron-capture dissociation, electron-transfer dissociation), and through commercialization of new or improved mass analyzers such as the Orbitrap, linear traps, quadrupole TOFs or Fourier transform ion cyclotron resonance.

    SDS Page:

    Article Title: Intact proteome fractionation strategies compatible with mass spectrometry.
    Article Snippet: www.expert-reviews.com ISSN 1478-9450 © 2011 Expert Reviews Ltd 10.1586/EPR.11.67 Within its approximately 20-year history, proteome analysis has been aided primarily through instrumental advances.. Relative to the instrumentation used in the first peptide mass fingerprinting and peptide sequencing experiments, today’s mass spectrometers scan faster, and are more sensitive, selective and versatile than ever before.. Sparked by the development of soft ionization (i.e., MALDI, ESI), biological mass spectrometry (MS) has evolved through novel fragmentation strategies (electron-capture dissociation, electron-transfer dissociation), and through commercialization of new or improved mass analyzers such as the Orbitrap, linear traps, quadrupole TOFs or Fourier transform ion cyclotron resonance.

    other:

    Article Title: Purification and characterisation of a novel protease from Cordyceps sinensis and determination of the cleavage site motifs using oriented peptide library mixtures
    Article Snippet: A novel protease, from the edible fungus Cordyceps sinensis, was purified and characterised.. Its cleavage site motifs were determined by oriented peptide library mixtures and validated by synthetic peptides and natural proteins.. The protease was purified to homogeneity using anion-exchange chromatography, sieve chromatography, native PAGE and reversion phase chromatography.



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