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yeast h2b boster biological technology m30930 ab 2924769  (Boster Bio)


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    Boster Bio yeast h2b boster biological technology m30930 ab 2924769
    Yeast H2b Boster Biological Technology M30930 Ab 2924769, supplied by Boster Bio, used in various techniques. Bioz Stars score: 92/100, based on 3 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/yeast h2b boster biological technology m30930 ab 2924769/product/Boster Bio
    Average 92 stars, based on 3 article reviews
    yeast h2b boster biological technology m30930 ab 2924769 - by Bioz Stars, 2026-02
    92/100 stars

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    Workflow for the quantitative assessment of histone H2B monoubiquitination using immunoblot.

    Journal: Methods and Protocols

    Article Title: Quantitative Assessment of Histone H2B Monoubiquitination in Yeast Using Immunoblotting

    doi: 10.3390/mps5050074

    Figure Lengend Snippet: Workflow for the quantitative assessment of histone H2B monoubiquitination using immunoblot.

    Article Snippet: Unlike with the S. cerevisiae extracts ( and ), the anti-yeast histone H2B antibody (Active Motif; 1:1000) yielded high background or cross-reactivity when applied to the S. pombe extracts ( a, first panel).

    Techniques: Western Blot

    Detection of H2BK123ub1 in the indicated wild-type (WT) and mutant S. cerevisiae strains.( a ) Entire membrane probed with anti-yeast H2B (Active Motif) antibody (1:1000 dilution). ( b ) Sections of membrane probed with anti-yeast H2B (Active Motif) antibody at 1:1000 dilution (upper blot) and 1:10,000 (lower blot). Black arrow , H2BK123 monoubiquitinated form. Grey arrow, diubiquitinated form of H2B. ( c ) Section of membrane probed with anti-ubiquityl-H2B (K120) (Cell Signaling Technology) antibody (1:1000). Proteins stained with Ponceau S serve as loading controls. Molecular weights (kDa) based on protein size makers are indicated to the left of each blot. Asterisk, unspecific cross-reacting protein.

    Journal: Methods and Protocols

    Article Title: Quantitative Assessment of Histone H2B Monoubiquitination in Yeast Using Immunoblotting

    doi: 10.3390/mps5050074

    Figure Lengend Snippet: Detection of H2BK123ub1 in the indicated wild-type (WT) and mutant S. cerevisiae strains.( a ) Entire membrane probed with anti-yeast H2B (Active Motif) antibody (1:1000 dilution). ( b ) Sections of membrane probed with anti-yeast H2B (Active Motif) antibody at 1:1000 dilution (upper blot) and 1:10,000 (lower blot). Black arrow , H2BK123 monoubiquitinated form. Grey arrow, diubiquitinated form of H2B. ( c ) Section of membrane probed with anti-ubiquityl-H2B (K120) (Cell Signaling Technology) antibody (1:1000). Proteins stained with Ponceau S serve as loading controls. Molecular weights (kDa) based on protein size makers are indicated to the left of each blot. Asterisk, unspecific cross-reacting protein.

    Article Snippet: Unlike with the S. cerevisiae extracts ( and ), the anti-yeast histone H2B antibody (Active Motif; 1:1000) yielded high background or cross-reactivity when applied to the S. pombe extracts ( a, first panel).

    Techniques: Mutagenesis, Membrane, Staining

    Antibody dilutions used.

    Journal: Methods and Protocols

    Article Title: Quantitative Assessment of Histone H2B Monoubiquitination in Yeast Using Immunoblotting

    doi: 10.3390/mps5050074

    Figure Lengend Snippet: Antibody dilutions used.

    Article Snippet: Unlike with the S. cerevisiae extracts ( and ), the anti-yeast histone H2B antibody (Active Motif; 1:1000) yielded high background or cross-reactivity when applied to the S. pombe extracts ( a, first panel).

    Techniques:

    ( a ) Sections of membrane probed with the indicated antibodies to quantify histones H3 or H2B and H2BK123ub1 levels in wild-type (WT) and indicated deubiquitinase mutant S. cerevisiae strains. The antibody dilutions used are listed in . ( b ) Quantitation of histones H3 (i) and H2BK123ub1 (ii) levels normalized to Ponceau S stained proteins from two or three independent experiments, respectively. ( c ) Sections of membrane probed with anti-H2B antibody (1:1000 dilution) (upper), anti-ubiquityl H2BK120 antibody (1:1000) (middle), and stained with Ponceau S (lower) using extracts prepared from S. cerevisiae strains expressing untagged or C-terminal V5 epitope-tagged histone H2B.

    Journal: Methods and Protocols

    Article Title: Quantitative Assessment of Histone H2B Monoubiquitination in Yeast Using Immunoblotting

    doi: 10.3390/mps5050074

    Figure Lengend Snippet: ( a ) Sections of membrane probed with the indicated antibodies to quantify histones H3 or H2B and H2BK123ub1 levels in wild-type (WT) and indicated deubiquitinase mutant S. cerevisiae strains. The antibody dilutions used are listed in . ( b ) Quantitation of histones H3 (i) and H2BK123ub1 (ii) levels normalized to Ponceau S stained proteins from two or three independent experiments, respectively. ( c ) Sections of membrane probed with anti-H2B antibody (1:1000 dilution) (upper), anti-ubiquityl H2BK120 antibody (1:1000) (middle), and stained with Ponceau S (lower) using extracts prepared from S. cerevisiae strains expressing untagged or C-terminal V5 epitope-tagged histone H2B.

    Article Snippet: Unlike with the S. cerevisiae extracts ( and ), the anti-yeast histone H2B antibody (Active Motif; 1:1000) yielded high background or cross-reactivity when applied to the S. pombe extracts ( a, first panel).

    Techniques: Membrane, Mutagenesis, Quantitation Assay, Staining, Expressing

    ( a ) Samples from extracts prepared from S. pombe strains expressing untagged H2B or Flag-tagged H2B were spearated and transferred onto a PVDF membrane. Shown are whole or sections of membrane probed with anti-histone H2B antibody from Active Motif and from Gene Tex and with anti-H2BK120 ubiquityl antibody. Ponceau S dye-stained sections used for normalization are also shown. Asterisk indicates cross-reacting proteins. ( b ) Samples from extracts prepared from wild-type S. pombe or strains lacking Ubp8 or Brl1 were separated and transferred to PVDF membrane. Shown are sections of membrane probed with anti-H2B (Gene Tex) or anti-H2BK120 ubiquityl antibody are shown. A section of the membrane stained with Ponceau S used for normalization is also shown. ( c ) Quantitation of H2BK119ub1 levels in the S. pombe ubp8-null mutant relative to wild-type (WT) strain. Error bars denote standard deviation of the mean from three independent experiments.

    Journal: Methods and Protocols

    Article Title: Quantitative Assessment of Histone H2B Monoubiquitination in Yeast Using Immunoblotting

    doi: 10.3390/mps5050074

    Figure Lengend Snippet: ( a ) Samples from extracts prepared from S. pombe strains expressing untagged H2B or Flag-tagged H2B were spearated and transferred onto a PVDF membrane. Shown are whole or sections of membrane probed with anti-histone H2B antibody from Active Motif and from Gene Tex and with anti-H2BK120 ubiquityl antibody. Ponceau S dye-stained sections used for normalization are also shown. Asterisk indicates cross-reacting proteins. ( b ) Samples from extracts prepared from wild-type S. pombe or strains lacking Ubp8 or Brl1 were separated and transferred to PVDF membrane. Shown are sections of membrane probed with anti-H2B (Gene Tex) or anti-H2BK120 ubiquityl antibody are shown. A section of the membrane stained with Ponceau S used for normalization is also shown. ( c ) Quantitation of H2BK119ub1 levels in the S. pombe ubp8-null mutant relative to wild-type (WT) strain. Error bars denote standard deviation of the mean from three independent experiments.

    Article Snippet: Unlike with the S. cerevisiae extracts ( and ), the anti-yeast histone H2B antibody (Active Motif; 1:1000) yielded high background or cross-reactivity when applied to the S. pombe extracts ( a, first panel).

    Techniques: Expressing, Membrane, Staining, Quantitation Assay, Mutagenesis, Standard Deviation