mouse anti human rps3 Search Results


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    Santa Cruz Biotechnology anti rps3
    ( A ) Total protein lysates from WT and RNH1 KO of hematopoietic and non–hematopoietic-origin cell lines were analyzed by Western blot with the indicated antibodies. Blots are representative of three independent experiments. ( B ) Schematic showing total and polysomal RNA isolation and RNA-seq analysis. ( C and D ) The expression of ribosomal and nonribosomal genes in WT and RNH1 KO K562 cells obtained by polysomal RNA-seq (C) or total RNA-seq (D). Total genes with cutoff of P adj < 0.1 in polysomal RNA-seq and total RNA-seq were selected and plotted. Dotted lines separate genes with log 2 (fold change) <1 and >1. ( E and F ) Plot of log 2 (fold change) of total RNA versus translational activity (TA) of ribosomal and nonribosomal genes in WT (E) or RNH1 KO (F) samples. Horizontal dotted lines separate genes with log 2 (fold change) <1 and >1. Vertical lines separate genes with arbitrary cutoff of >7 or <7 for log 2 (expression in total RNA-seq). ( G ) The heat maps generated via Metascape tool with default parameters show the relative expression of genes in different gene ontology (GO) gene sets. ( H ) Protein lysates from K562 and HeLa with WT and RNH1 KO genotypes were analyzed by Western blot for RPS19, <t>RPS3,</t> and RNH1. Blots are representative of three independent experiments. GAPDH is used as a normalizing control, and numbers represent the normalized band intensity with respect to the corresponding WT sample. ( I ) Protein lysates from WT and Rnh1 −/− bone marrow (BM) and liver were analyzed by Western blot for RPS19, <t>RPS3,</t> and RNH1 ( N = 3 mice). GAPDH is used as a normalizing control, and numbers represent the normalized band intensity with respect to the corresponding WT sample.
    Anti Rps3, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/anti rps3/product/Santa Cruz Biotechnology
    Average 86 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    anti rps3 - by Bioz Stars, 2024-07
    86/100 stars
      Buy from Supplier

    86
    Santa Cruz Biotechnology rps3
    ( A ) Total protein lysates from WT and RNH1 KO of hematopoietic and non–hematopoietic-origin cell lines were analyzed by Western blot with the indicated antibodies. Blots are representative of three independent experiments. ( B ) Schematic showing total and polysomal RNA isolation and RNA-seq analysis. ( C and D ) The expression of ribosomal and nonribosomal genes in WT and RNH1 KO K562 cells obtained by polysomal RNA-seq (C) or total RNA-seq (D). Total genes with cutoff of P adj < 0.1 in polysomal RNA-seq and total RNA-seq were selected and plotted. Dotted lines separate genes with log 2 (fold change) <1 and >1. ( E and F ) Plot of log 2 (fold change) of total RNA versus translational activity (TA) of ribosomal and nonribosomal genes in WT (E) or RNH1 KO (F) samples. Horizontal dotted lines separate genes with log 2 (fold change) <1 and >1. Vertical lines separate genes with arbitrary cutoff of >7 or <7 for log 2 (expression in total RNA-seq). ( G ) The heat maps generated via Metascape tool with default parameters show the relative expression of genes in different gene ontology (GO) gene sets. ( H ) Protein lysates from K562 and HeLa with WT and RNH1 KO genotypes were analyzed by Western blot for RPS19, <t>RPS3,</t> and RNH1. Blots are representative of three independent experiments. GAPDH is used as a normalizing control, and numbers represent the normalized band intensity with respect to the corresponding WT sample. ( I ) Protein lysates from WT and Rnh1 −/− bone marrow (BM) and liver were analyzed by Western blot for RPS19, <t>RPS3,</t> and RNH1 ( N = 3 mice). GAPDH is used as a normalizing control, and numbers represent the normalized band intensity with respect to the corresponding WT sample.
    Rps3, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/rps3/product/Santa Cruz Biotechnology
    Average 86 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    rps3 - by Bioz Stars, 2024-07
    86/100 stars
      Buy from Supplier

    86
    Bethyl rps3 rabbit polyclonal antibody
    ( A ) Total protein lysates from WT and RNH1 KO of hematopoietic and non–hematopoietic-origin cell lines were analyzed by Western blot with the indicated antibodies. Blots are representative of three independent experiments. ( B ) Schematic showing total and polysomal RNA isolation and RNA-seq analysis. ( C and D ) The expression of ribosomal and nonribosomal genes in WT and RNH1 KO K562 cells obtained by polysomal RNA-seq (C) or total RNA-seq (D). Total genes with cutoff of P adj < 0.1 in polysomal RNA-seq and total RNA-seq were selected and plotted. Dotted lines separate genes with log 2 (fold change) <1 and >1. ( E and F ) Plot of log 2 (fold change) of total RNA versus translational activity (TA) of ribosomal and nonribosomal genes in WT (E) or RNH1 KO (F) samples. Horizontal dotted lines separate genes with log 2 (fold change) <1 and >1. Vertical lines separate genes with arbitrary cutoff of >7 or <7 for log 2 (expression in total RNA-seq). ( G ) The heat maps generated via Metascape tool with default parameters show the relative expression of genes in different gene ontology (GO) gene sets. ( H ) Protein lysates from K562 and HeLa with WT and RNH1 KO genotypes were analyzed by Western blot for RPS19, <t>RPS3,</t> and RNH1. Blots are representative of three independent experiments. GAPDH is used as a normalizing control, and numbers represent the normalized band intensity with respect to the corresponding WT sample. ( I ) Protein lysates from WT and Rnh1 −/− bone marrow (BM) and liver were analyzed by Western blot for RPS19, <t>RPS3,</t> and RNH1 ( N = 3 mice). GAPDH is used as a normalizing control, and numbers represent the normalized band intensity with respect to the corresponding WT sample.
    Rps3 Rabbit Polyclonal Antibody, supplied by Bethyl, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/rps3 rabbit polyclonal antibody/product/Bethyl
    Average 86 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    rps3 rabbit polyclonal antibody - by Bioz Stars, 2024-07
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    86
    Cell Signaling Technology Inc rabbit anti rps3

    Rabbit Anti Rps3, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/rabbit anti rps3/product/Cell Signaling Technology Inc
    Average 86 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    rabbit anti rps3 - by Bioz Stars, 2024-07
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    Image Search Results


    ( A ) Total protein lysates from WT and RNH1 KO of hematopoietic and non–hematopoietic-origin cell lines were analyzed by Western blot with the indicated antibodies. Blots are representative of three independent experiments. ( B ) Schematic showing total and polysomal RNA isolation and RNA-seq analysis. ( C and D ) The expression of ribosomal and nonribosomal genes in WT and RNH1 KO K562 cells obtained by polysomal RNA-seq (C) or total RNA-seq (D). Total genes with cutoff of P adj < 0.1 in polysomal RNA-seq and total RNA-seq were selected and plotted. Dotted lines separate genes with log 2 (fold change) <1 and >1. ( E and F ) Plot of log 2 (fold change) of total RNA versus translational activity (TA) of ribosomal and nonribosomal genes in WT (E) or RNH1 KO (F) samples. Horizontal dotted lines separate genes with log 2 (fold change) <1 and >1. Vertical lines separate genes with arbitrary cutoff of >7 or <7 for log 2 (expression in total RNA-seq). ( G ) The heat maps generated via Metascape tool with default parameters show the relative expression of genes in different gene ontology (GO) gene sets. ( H ) Protein lysates from K562 and HeLa with WT and RNH1 KO genotypes were analyzed by Western blot for RPS19, RPS3, and RNH1. Blots are representative of three independent experiments. GAPDH is used as a normalizing control, and numbers represent the normalized band intensity with respect to the corresponding WT sample. ( I ) Protein lysates from WT and Rnh1 −/− bone marrow (BM) and liver were analyzed by Western blot for RPS19, RPS3, and RNH1 ( N = 3 mice). GAPDH is used as a normalizing control, and numbers represent the normalized band intensity with respect to the corresponding WT sample.

    Journal: Science Advances

    Article Title: Ribonuclease inhibitor and angiogenin system regulates cell type–specific global translation

    doi: 10.1126/sciadv.adl0320

    Figure Lengend Snippet: ( A ) Total protein lysates from WT and RNH1 KO of hematopoietic and non–hematopoietic-origin cell lines were analyzed by Western blot with the indicated antibodies. Blots are representative of three independent experiments. ( B ) Schematic showing total and polysomal RNA isolation and RNA-seq analysis. ( C and D ) The expression of ribosomal and nonribosomal genes in WT and RNH1 KO K562 cells obtained by polysomal RNA-seq (C) or total RNA-seq (D). Total genes with cutoff of P adj < 0.1 in polysomal RNA-seq and total RNA-seq were selected and plotted. Dotted lines separate genes with log 2 (fold change) <1 and >1. ( E and F ) Plot of log 2 (fold change) of total RNA versus translational activity (TA) of ribosomal and nonribosomal genes in WT (E) or RNH1 KO (F) samples. Horizontal dotted lines separate genes with log 2 (fold change) <1 and >1. Vertical lines separate genes with arbitrary cutoff of >7 or <7 for log 2 (expression in total RNA-seq). ( G ) The heat maps generated via Metascape tool with default parameters show the relative expression of genes in different gene ontology (GO) gene sets. ( H ) Protein lysates from K562 and HeLa with WT and RNH1 KO genotypes were analyzed by Western blot for RPS19, RPS3, and RNH1. Blots are representative of three independent experiments. GAPDH is used as a normalizing control, and numbers represent the normalized band intensity with respect to the corresponding WT sample. ( I ) Protein lysates from WT and Rnh1 −/− bone marrow (BM) and liver were analyzed by Western blot for RPS19, RPS3, and RNH1 ( N = 3 mice). GAPDH is used as a normalizing control, and numbers represent the normalized band intensity with respect to the corresponding WT sample.

    Article Snippet: Anti-RPS3 , Human, mouse , Santa Cruz Biotechnology , sc-376008.

    Techniques: Western Blot, Isolation, RNA Sequencing Assay, Expressing, Activity Assay, Generated

    Antibodies: Details of the antibodies used in the study.

    Journal: Science Advances

    Article Title: Ribonuclease inhibitor and angiogenin system regulates cell type–specific global translation

    doi: 10.1126/sciadv.adl0320

    Figure Lengend Snippet: Antibodies: Details of the antibodies used in the study.

    Article Snippet: Anti-RPS3 , Human, mouse , Santa Cruz Biotechnology , sc-376008.

    Techniques:

    Journal: eLife

    Article Title: Paradoxical imbalance between activated lymphocyte protein synthesis capacity and rapid division rate

    doi: 10.7554/eLife.89015

    Figure Lengend Snippet:

    Article Snippet: Depending on the experiment, we used the following primary antibodies: mouse anti-PMY (clone 2A4) at 6.66 μg/ml; human anti-ribosomal P antigen (Immunovision) at 1:2000; rabbit anti-RPL7 (Abcam) at 1:1000, rabbit anti-RPL26 (Bethyl Laboratories) at 1:2000; mouse anti-beta actin (Invitrogen) at 1:4000; rabbit anti-HSP90 (Santa Cruz) at 1:500; rat anti-GRP94 at 1:1500 (Enzo); rabbit anti-RPL28 (Abcam) at 1:500, rabbit anti-RPL6 (Abcam) at 1:1000, mouse anti-PDI at 1: 2000 (Abcam); mouse anti-lamin A/C (Cell Signaling Technology) at 1: 2000, rabbit anti-fibrillarin (Cell Signaling Technology) at 1:1000, mouse anti-RPS6 (Cell Signaling Technology) at 1:1000, rabbit anti-histone H3 (Cell Signaling Technology) at 1: 2000, rabbit anti-RPL5 (Cell Signaling Technology) at 1:1000, and rabbit anti-RPS3 (Cell Signaling Technology) at 1:1000 (Cell Signaling Technology).

    Techniques: Transgenic Assay, Western Blot, Recombinant, Activation Assay, Virus, DC Protein Assay