rabbit polyclonal anti ub h2b  (Cell Signaling Technology Inc)


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    Structured Review

    Cell Signaling Technology Inc rabbit polyclonal anti ub h2b
    (A) Western blotting of ub-H2A, <t>ub-H2B,</t> and H4K16ac in late spermatids from dpp 12-week mice with H3K27me3 as a loading control. Quantification of blotting intensity for indicated proteins is shown in parentheses (the one in Miwi+/DB control is set as 100% after normalization with H3K27me3 blotting).
    Rabbit Polyclonal Anti Ub H2b, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/rabbit polyclonal anti ub h2b/product/Cell Signaling Technology Inc
    Average 95 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    rabbit polyclonal anti ub h2b - by Bioz Stars, 2023-09
    95/100 stars

    Images

    1) Product Images from "Ubiquitination-Deficient Mutations in Human Piwi Cause Male Infertility by Impairing Histone-to-Protamine Exchange during Spermiogenesis"

    Article Title: Ubiquitination-Deficient Mutations in Human Piwi Cause Male Infertility by Impairing Histone-to-Protamine Exchange during Spermiogenesis

    Journal: Cell

    doi: 10.1016/j.cell.2017.04.034

    (A) Western blotting of ub-H2A, ub-H2B, and H4K16ac in late spermatids from dpp 12-week mice with H3K27me3 as a loading control. Quantification of blotting intensity for indicated proteins is shown in parentheses (the one in Miwi+/DB control is set as 100% after normalization with H3K27me3 blotting).
    Figure Legend Snippet: (A) Western blotting of ub-H2A, ub-H2B, and H4K16ac in late spermatids from dpp 12-week mice with H3K27me3 as a loading control. Quantification of blotting intensity for indicated proteins is shown in parentheses (the one in Miwi+/DB control is set as 100% after normalization with H3K27me3 blotting).

    Techniques Used: Western Blot

    (A–C) Immunostaining of endogenous RNF8 (A), (red) or ub-H2B (B), (red) in late spermatids (LS) and H2B in sperm (C), (red) from Miwi+/DB-Cre males transduced by RNF8-N:Cyto IV-EGFP (left) or RNF8-Nmut:Cyto IV-EGFP (right), with nuclei counterstained by DAPI (blue). Left lanes in each staining panel show the representative staining images, and GFP (green) and arrows indicate cells that were successfully transduced with the respective constructs; right lanes show an enlarged view of the representative cells. Right panels: quantification of late spermatids showing visible RNF8 nucleus translocation (A) or ub-H2B staining (B), and sperm without H2B staining (C), top) or with normal morphology (C), bottom) among GFP+ or GFP− cells (n = 100 per group; the average values ± SD of three separate experiments are plotted). Scale bar, 10 μm.
    Figure Legend Snippet: (A–C) Immunostaining of endogenous RNF8 (A), (red) or ub-H2B (B), (red) in late spermatids (LS) and H2B in sperm (C), (red) from Miwi+/DB-Cre males transduced by RNF8-N:Cyto IV-EGFP (left) or RNF8-Nmut:Cyto IV-EGFP (right), with nuclei counterstained by DAPI (blue). Left lanes in each staining panel show the representative staining images, and GFP (green) and arrows indicate cells that were successfully transduced with the respective constructs; right lanes show an enlarged view of the representative cells. Right panels: quantification of late spermatids showing visible RNF8 nucleus translocation (A) or ub-H2B staining (B), and sperm without H2B staining (C), top) or with normal morphology (C), bottom) among GFP+ or GFP− cells (n = 100 per group; the average values ± SD of three separate experiments are plotted). Scale bar, 10 μm.

    Techniques Used: Immunostaining, Staining, Transduction, Construct, Translocation Assay

    Key Resources Table
    Figure Legend Snippet: Key Resources Table

    Techniques Used: Recombinant, In Situ, Sequencing, Software

    rabbit polyclonal anti ub h2b  (Cell Signaling Technology Inc)


    Bioz Verified Symbol Cell Signaling Technology Inc is a verified supplier
    Bioz Manufacturer Symbol Cell Signaling Technology Inc manufactures this product  
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  • About
  • News
  • Press Release
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  • Advisors
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  • 95

    Structured Review

    Cell Signaling Technology Inc rabbit polyclonal anti ub h2b
    (A) Western blotting of ub-H2A, <t>ub-H2B,</t> and H4K16ac in late spermatids from dpp 12-week mice with H3K27me3 as a loading control. Quantification of blotting intensity for indicated proteins is shown in parentheses (the one in Miwi+/DB control is set as 100% after normalization with H3K27me3 blotting).
    Rabbit Polyclonal Anti Ub H2b, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/rabbit polyclonal anti ub h2b/product/Cell Signaling Technology Inc
    Average 95 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    rabbit polyclonal anti ub h2b - by Bioz Stars, 2023-09
    95/100 stars

    Images

    1) Product Images from "Ubiquitination-Deficient Mutations in Human Piwi Cause Male Infertility by Impairing Histone-to-Protamine Exchange during Spermiogenesis"

    Article Title: Ubiquitination-Deficient Mutations in Human Piwi Cause Male Infertility by Impairing Histone-to-Protamine Exchange during Spermiogenesis

    Journal: Cell

    doi: 10.1016/j.cell.2017.04.034

    (A) Western blotting of ub-H2A, ub-H2B, and H4K16ac in late spermatids from dpp 12-week mice with H3K27me3 as a loading control. Quantification of blotting intensity for indicated proteins is shown in parentheses (the one in Miwi+/DB control is set as 100% after normalization with H3K27me3 blotting).
    Figure Legend Snippet: (A) Western blotting of ub-H2A, ub-H2B, and H4K16ac in late spermatids from dpp 12-week mice with H3K27me3 as a loading control. Quantification of blotting intensity for indicated proteins is shown in parentheses (the one in Miwi+/DB control is set as 100% after normalization with H3K27me3 blotting).

    Techniques Used: Western Blot

    (A–C) Immunostaining of endogenous RNF8 (A), (red) or ub-H2B (B), (red) in late spermatids (LS) and H2B in sperm (C), (red) from Miwi+/DB-Cre males transduced by RNF8-N:Cyto IV-EGFP (left) or RNF8-Nmut:Cyto IV-EGFP (right), with nuclei counterstained by DAPI (blue). Left lanes in each staining panel show the representative staining images, and GFP (green) and arrows indicate cells that were successfully transduced with the respective constructs; right lanes show an enlarged view of the representative cells. Right panels: quantification of late spermatids showing visible RNF8 nucleus translocation (A) or ub-H2B staining (B), and sperm without H2B staining (C), top) or with normal morphology (C), bottom) among GFP+ or GFP− cells (n = 100 per group; the average values ± SD of three separate experiments are plotted). Scale bar, 10 μm.
    Figure Legend Snippet: (A–C) Immunostaining of endogenous RNF8 (A), (red) or ub-H2B (B), (red) in late spermatids (LS) and H2B in sperm (C), (red) from Miwi+/DB-Cre males transduced by RNF8-N:Cyto IV-EGFP (left) or RNF8-Nmut:Cyto IV-EGFP (right), with nuclei counterstained by DAPI (blue). Left lanes in each staining panel show the representative staining images, and GFP (green) and arrows indicate cells that were successfully transduced with the respective constructs; right lanes show an enlarged view of the representative cells. Right panels: quantification of late spermatids showing visible RNF8 nucleus translocation (A) or ub-H2B staining (B), and sperm without H2B staining (C), top) or with normal morphology (C), bottom) among GFP+ or GFP− cells (n = 100 per group; the average values ± SD of three separate experiments are plotted). Scale bar, 10 μm.

    Techniques Used: Immunostaining, Staining, Transduction, Construct, Translocation Assay

    Key Resources Table
    Figure Legend Snippet: Key Resources Table

    Techniques Used: Recombinant, In Situ, Sequencing, Software

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    Cell Signaling Technology Inc rabbit polyclonal anti ub h2b
    (A) Western blotting of ub-H2A, <t>ub-H2B,</t> and H4K16ac in late spermatids from dpp 12-week mice with H3K27me3 as a loading control. Quantification of blotting intensity for indicated proteins is shown in parentheses (the one in Miwi+/DB control is set as 100% after normalization with H3K27me3 blotting).
    Rabbit Polyclonal Anti Ub H2b, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/rabbit polyclonal anti ub h2b/product/Cell Signaling Technology Inc
    Average 95 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    rabbit polyclonal anti ub h2b - by Bioz Stars, 2023-09
    95/100 stars
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    Image Search Results


    (A) Western blotting of ub-H2A, ub-H2B, and H4K16ac in late spermatids from dpp 12-week mice with H3K27me3 as a loading control. Quantification of blotting intensity for indicated proteins is shown in parentheses (the one in Miwi+/DB control is set as 100% after normalization with H3K27me3 blotting).

    Journal: Cell

    Article Title: Ubiquitination-Deficient Mutations in Human Piwi Cause Male Infertility by Impairing Histone-to-Protamine Exchange during Spermiogenesis

    doi: 10.1016/j.cell.2017.04.034

    Figure Lengend Snippet: (A) Western blotting of ub-H2A, ub-H2B, and H4K16ac in late spermatids from dpp 12-week mice with H3K27me3 as a loading control. Quantification of blotting intensity for indicated proteins is shown in parentheses (the one in Miwi+/DB control is set as 100% after normalization with H3K27me3 blotting).

    Article Snippet: Rabbit polyclonal anti-ub-H2B , Cell Signaling Technology , Cat#5546; RRID:AB_10693452.

    Techniques: Western Blot

    (A–C) Immunostaining of endogenous RNF8 (A), (red) or ub-H2B (B), (red) in late spermatids (LS) and H2B in sperm (C), (red) from Miwi+/DB-Cre males transduced by RNF8-N:Cyto IV-EGFP (left) or RNF8-Nmut:Cyto IV-EGFP (right), with nuclei counterstained by DAPI (blue). Left lanes in each staining panel show the representative staining images, and GFP (green) and arrows indicate cells that were successfully transduced with the respective constructs; right lanes show an enlarged view of the representative cells. Right panels: quantification of late spermatids showing visible RNF8 nucleus translocation (A) or ub-H2B staining (B), and sperm without H2B staining (C), top) or with normal morphology (C), bottom) among GFP+ or GFP− cells (n = 100 per group; the average values ± SD of three separate experiments are plotted). Scale bar, 10 μm.

    Journal: Cell

    Article Title: Ubiquitination-Deficient Mutations in Human Piwi Cause Male Infertility by Impairing Histone-to-Protamine Exchange during Spermiogenesis

    doi: 10.1016/j.cell.2017.04.034

    Figure Lengend Snippet: (A–C) Immunostaining of endogenous RNF8 (A), (red) or ub-H2B (B), (red) in late spermatids (LS) and H2B in sperm (C), (red) from Miwi+/DB-Cre males transduced by RNF8-N:Cyto IV-EGFP (left) or RNF8-Nmut:Cyto IV-EGFP (right), with nuclei counterstained by DAPI (blue). Left lanes in each staining panel show the representative staining images, and GFP (green) and arrows indicate cells that were successfully transduced with the respective constructs; right lanes show an enlarged view of the representative cells. Right panels: quantification of late spermatids showing visible RNF8 nucleus translocation (A) or ub-H2B staining (B), and sperm without H2B staining (C), top) or with normal morphology (C), bottom) among GFP+ or GFP− cells (n = 100 per group; the average values ± SD of three separate experiments are plotted). Scale bar, 10 μm.

    Article Snippet: Rabbit polyclonal anti-ub-H2B , Cell Signaling Technology , Cat#5546; RRID:AB_10693452.

    Techniques: Immunostaining, Staining, Transduction, Construct, Translocation Assay

    Key Resources Table

    Journal: Cell

    Article Title: Ubiquitination-Deficient Mutations in Human Piwi Cause Male Infertility by Impairing Histone-to-Protamine Exchange during Spermiogenesis

    doi: 10.1016/j.cell.2017.04.034

    Figure Lengend Snippet: Key Resources Table

    Article Snippet: Rabbit polyclonal anti-ub-H2B , Cell Signaling Technology , Cat#5546; RRID:AB_10693452.

    Techniques: Recombinant, In Situ, Sequencing, Software