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protein structure rps7  (Databank Inc)

 
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    Structured Review

    Databank Inc protein structure rps7
    BC-3 target proteins analyzed by mass spectrometry. ( A ) The binding of biotin- and FITC-labeled BC-3 to 5637 cells was measured by flow cytometry, with biotin- and FITC-labeled Library as a control. ( B ) SDS-PAGE with silver staining was used to identify the aptamer target. Lane library, protein captured with biotin-labeled library treated sample; Lane BC-3, protein captured with biotin-labeled BC-3 treated sample. ( C ) Western blot analysis of the concentrations of <t>RPS7</t> and β-actin in the preparations captured via Library and BC-3. ( D ) After incubating the ER fluorescence probe ER-tracker (red) for 0.5 h and FITC-labeled BC-3 or Library (green) for 1 h, 5637 cells displayed the colocalization (yellow) of ER-tracker and FITC-labeled BC-3. ( E ) Enlarged view of intracellular fluorescence signals in colocalization. ( F ) Fluorescence intensity profile of yellow arrow regions in 5637 cells (scale bar = 40 μm).
    Protein Structure Rps7, supplied by Databank Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/protein structure rps7/product/Databank Inc
    Average 90 stars, based on 1 article reviews
    protein structure rps7 - by Bioz Stars, 2026-05
    90/100 stars

    Images

    1) Product Images from "Identification of new aptamer BC-3 targeting RPS7 from rapid screening for bladder carcinoma"

    Article Title: Identification of new aptamer BC-3 targeting RPS7 from rapid screening for bladder carcinoma

    Journal: Genes & Diseases

    doi: 10.1016/j.gendis.2022.07.002

    BC-3 target proteins analyzed by mass spectrometry. ( A ) The binding of biotin- and FITC-labeled BC-3 to 5637 cells was measured by flow cytometry, with biotin- and FITC-labeled Library as a control. ( B ) SDS-PAGE with silver staining was used to identify the aptamer target. Lane library, protein captured with biotin-labeled library treated sample; Lane BC-3, protein captured with biotin-labeled BC-3 treated sample. ( C ) Western blot analysis of the concentrations of RPS7 and β-actin in the preparations captured via Library and BC-3. ( D ) After incubating the ER fluorescence probe ER-tracker (red) for 0.5 h and FITC-labeled BC-3 or Library (green) for 1 h, 5637 cells displayed the colocalization (yellow) of ER-tracker and FITC-labeled BC-3. ( E ) Enlarged view of intracellular fluorescence signals in colocalization. ( F ) Fluorescence intensity profile of yellow arrow regions in 5637 cells (scale bar = 40 μm).
    Figure Legend Snippet: BC-3 target proteins analyzed by mass spectrometry. ( A ) The binding of biotin- and FITC-labeled BC-3 to 5637 cells was measured by flow cytometry, with biotin- and FITC-labeled Library as a control. ( B ) SDS-PAGE with silver staining was used to identify the aptamer target. Lane library, protein captured with biotin-labeled library treated sample; Lane BC-3, protein captured with biotin-labeled BC-3 treated sample. ( C ) Western blot analysis of the concentrations of RPS7 and β-actin in the preparations captured via Library and BC-3. ( D ) After incubating the ER fluorescence probe ER-tracker (red) for 0.5 h and FITC-labeled BC-3 or Library (green) for 1 h, 5637 cells displayed the colocalization (yellow) of ER-tracker and FITC-labeled BC-3. ( E ) Enlarged view of intracellular fluorescence signals in colocalization. ( F ) Fluorescence intensity profile of yellow arrow regions in 5637 cells (scale bar = 40 μm).

    Techniques Used: Mass Spectrometry, Binding Assay, Labeling, Flow Cytometry, Control, SDS Page, Silver Staining, Western Blot, Fluorescence

    Computational analysis of the Binding Model between RPS7 and BC-3. ( A ) Interaction model between RPS7 and BC-3. Close view of the RPS7 and BC-3 interaction region in part α and part β with key amino acid residues marked. Promoter methylation ( B ) and the expression level ( C ) of RPS7 in bladder cancer and normal bladder samples from TCGA.
    Figure Legend Snippet: Computational analysis of the Binding Model between RPS7 and BC-3. ( A ) Interaction model between RPS7 and BC-3. Close view of the RPS7 and BC-3 interaction region in part α and part β with key amino acid residues marked. Promoter methylation ( B ) and the expression level ( C ) of RPS7 in bladder cancer and normal bladder samples from TCGA.

    Techniques Used: Binding Assay, Methylation, Expressing



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    protein structure rps7  (Databank Inc)
    90
    Databank Inc protein structure rps7
    BC-3 target proteins analyzed by mass spectrometry. ( A ) The binding of biotin- and FITC-labeled BC-3 to 5637 cells was measured by flow cytometry, with biotin- and FITC-labeled Library as a control. ( B ) SDS-PAGE with silver staining was used to identify the aptamer target. Lane library, protein captured with biotin-labeled library treated sample; Lane BC-3, protein captured with biotin-labeled BC-3 treated sample. ( C ) Western blot analysis of the concentrations of <t>RPS7</t> and β-actin in the preparations captured via Library and BC-3. ( D ) After incubating the ER fluorescence probe ER-tracker (red) for 0.5 h and FITC-labeled BC-3 or Library (green) for 1 h, 5637 cells displayed the colocalization (yellow) of ER-tracker and FITC-labeled BC-3. ( E ) Enlarged view of intracellular fluorescence signals in colocalization. ( F ) Fluorescence intensity profile of yellow arrow regions in 5637 cells (scale bar = 40 μm).
    Protein Structure Rps7, supplied by Databank Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/protein structure rps7/product/Databank Inc
    Average 90 stars, based on 1 article reviews
    protein structure rps7 - by Bioz Stars, 2026-05
    90/100 stars
    		  Buy from Supplier

    Image Search Results


    BC-3 target proteins analyzed by mass spectrometry. ( A ) The binding of biotin- and FITC-labeled BC-3 to 5637 cells was measured by flow cytometry, with biotin- and FITC-labeled Library as a control. ( B ) SDS-PAGE with silver staining was used to identify the aptamer target. Lane library, protein captured with biotin-labeled library treated sample; Lane BC-3, protein captured with biotin-labeled BC-3 treated sample. ( C ) Western blot analysis of the concentrations of RPS7 and β-actin in the preparations captured via Library and BC-3. ( D ) After incubating the ER fluorescence probe ER-tracker (red) for 0.5 h and FITC-labeled BC-3 or Library (green) for 1 h, 5637 cells displayed the colocalization (yellow) of ER-tracker and FITC-labeled BC-3. ( E ) Enlarged view of intracellular fluorescence signals in colocalization. ( F ) Fluorescence intensity profile of yellow arrow regions in 5637 cells (scale bar = 40 μm).

    Journal: Genes & Diseases

    Article Title: Identification of new aptamer BC-3 targeting RPS7 from rapid screening for bladder carcinoma

    doi: 10.1016/j.gendis.2022.07.002

    Figure Lengend Snippet: BC-3 target proteins analyzed by mass spectrometry. ( A ) The binding of biotin- and FITC-labeled BC-3 to 5637 cells was measured by flow cytometry, with biotin- and FITC-labeled Library as a control. ( B ) SDS-PAGE with silver staining was used to identify the aptamer target. Lane library, protein captured with biotin-labeled library treated sample; Lane BC-3, protein captured with biotin-labeled BC-3 treated sample. ( C ) Western blot analysis of the concentrations of RPS7 and β-actin in the preparations captured via Library and BC-3. ( D ) After incubating the ER fluorescence probe ER-tracker (red) for 0.5 h and FITC-labeled BC-3 or Library (green) for 1 h, 5637 cells displayed the colocalization (yellow) of ER-tracker and FITC-labeled BC-3. ( E ) Enlarged view of intracellular fluorescence signals in colocalization. ( F ) Fluorescence intensity profile of yellow arrow regions in 5637 cells (scale bar = 40 μm).

    Article Snippet: Firstly, the protein structure of RPS7 was downloaded from the RCSB PDB databank (PDB ID: 6YBW) with a resolution of 3.1 Å.

    Techniques: Mass Spectrometry, Binding Assay, Labeling, Flow Cytometry, Control, SDS Page, Silver Staining, Western Blot, Fluorescence

    Computational analysis of the Binding Model between RPS7 and BC-3. ( A ) Interaction model between RPS7 and BC-3. Close view of the RPS7 and BC-3 interaction region in part α and part β with key amino acid residues marked. Promoter methylation ( B ) and the expression level ( C ) of RPS7 in bladder cancer and normal bladder samples from TCGA.

    Journal: Genes & Diseases

    Article Title: Identification of new aptamer BC-3 targeting RPS7 from rapid screening for bladder carcinoma

    doi: 10.1016/j.gendis.2022.07.002

    Figure Lengend Snippet: Computational analysis of the Binding Model between RPS7 and BC-3. ( A ) Interaction model between RPS7 and BC-3. Close view of the RPS7 and BC-3 interaction region in part α and part β with key amino acid residues marked. Promoter methylation ( B ) and the expression level ( C ) of RPS7 in bladder cancer and normal bladder samples from TCGA.

    Article Snippet: Firstly, the protein structure of RPS7 was downloaded from the RCSB PDB databank (PDB ID: 6YBW) with a resolution of 3.1 Å.

    Techniques: Binding Assay, Methylation, Expressing