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prestained dual colour protein size marker  (tiangen biotech co)


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    tiangen biotech co prestained dual colour protein size marker
    In vitro protein‐binding assay of Papaya ringspot virus helper component‐proteinase (PRSV HC‐Pro) and Carica papaya calreticulin (PaCRT). In vitro translated biotinylated PaCRT was incubated with purified glutathione S‐transferase (GST) or GST‐PRSV HC‐Pro, which was immobilized on MagneGST particles. After incubation, the proteins interacting with GST or GST‐PRSV HC‐Pro were bound to the MagneGST particles. The eluted GST‐bound proteins (lane 4) or GST‐PRSV HC‐Pro‐bound proteins (lane 5) were then analysed by 10% sodium dodecylsulphate‐polyacrylamide gel electrophoresis (SDS‐PAGE) and probed with streptavidin‐alkaline phosphatase (streptavidin‐AP) (A) or anti‐GST antibody (B) (GST, 26.0 kDa; GST‐PRSV HC‐Pro, 78.0 kDa; biotinylated PaCRT, 48.2 kDa). The purified GST (lane 1), purified GST‐PRSV HC‐Pro (lane 2) and in vitro translated biotinylated PaCRT (lane 3) were used as controls, respectively. The <t>prestained</t> dual colour protein size marker (Tiangen) is indicated on the left of the panel.
    Prestained Dual Colour Protein Size Marker, supplied by tiangen biotech co, used in various techniques. Bioz Stars score: 86/100, based on 4 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/prestained dual colour protein size marker/product/tiangen biotech co
    Average 86 stars, based on 4 article reviews
    prestained dual colour protein size marker - by Bioz Stars, 2026-03
    86/100 stars

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    1) Product Images from "Helper component‐proteinase (HC‐Pro) protein of Papaya ringspot virus interacts with papaya calreticulin"

    Article Title: Helper component‐proteinase (HC‐Pro) protein of Papaya ringspot virus interacts with papaya calreticulin

    Journal: Molecular Plant Pathology

    doi: 10.1111/j.1364-3703.2009.00606.x

    In vitro protein‐binding assay of Papaya ringspot virus helper component‐proteinase (PRSV HC‐Pro) and Carica papaya calreticulin (PaCRT). In vitro translated biotinylated PaCRT was incubated with purified glutathione S‐transferase (GST) or GST‐PRSV HC‐Pro, which was immobilized on MagneGST particles. After incubation, the proteins interacting with GST or GST‐PRSV HC‐Pro were bound to the MagneGST particles. The eluted GST‐bound proteins (lane 4) or GST‐PRSV HC‐Pro‐bound proteins (lane 5) were then analysed by 10% sodium dodecylsulphate‐polyacrylamide gel electrophoresis (SDS‐PAGE) and probed with streptavidin‐alkaline phosphatase (streptavidin‐AP) (A) or anti‐GST antibody (B) (GST, 26.0 kDa; GST‐PRSV HC‐Pro, 78.0 kDa; biotinylated PaCRT, 48.2 kDa). The purified GST (lane 1), purified GST‐PRSV HC‐Pro (lane 2) and in vitro translated biotinylated PaCRT (lane 3) were used as controls, respectively. The prestained dual colour protein size marker (Tiangen) is indicated on the left of the panel.
    Figure Legend Snippet: In vitro protein‐binding assay of Papaya ringspot virus helper component‐proteinase (PRSV HC‐Pro) and Carica papaya calreticulin (PaCRT). In vitro translated biotinylated PaCRT was incubated with purified glutathione S‐transferase (GST) or GST‐PRSV HC‐Pro, which was immobilized on MagneGST particles. After incubation, the proteins interacting with GST or GST‐PRSV HC‐Pro were bound to the MagneGST particles. The eluted GST‐bound proteins (lane 4) or GST‐PRSV HC‐Pro‐bound proteins (lane 5) were then analysed by 10% sodium dodecylsulphate‐polyacrylamide gel electrophoresis (SDS‐PAGE) and probed with streptavidin‐alkaline phosphatase (streptavidin‐AP) (A) or anti‐GST antibody (B) (GST, 26.0 kDa; GST‐PRSV HC‐Pro, 78.0 kDa; biotinylated PaCRT, 48.2 kDa). The purified GST (lane 1), purified GST‐PRSV HC‐Pro (lane 2) and in vitro translated biotinylated PaCRT (lane 3) were used as controls, respectively. The prestained dual colour protein size marker (Tiangen) is indicated on the left of the panel.

    Techniques Used: In Vitro, Protein Binding, Incubation, Purification, Polyacrylamide Gel Electrophoresis, SDS Page, Marker



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    prestained dual colour protein size marker  (tiangen biotech co)
    86
    tiangen biotech co prestained dual colour protein size marker
    In vitro protein‐binding assay of Papaya ringspot virus helper component‐proteinase (PRSV HC‐Pro) and Carica papaya calreticulin (PaCRT). In vitro translated biotinylated PaCRT was incubated with purified glutathione S‐transferase (GST) or GST‐PRSV HC‐Pro, which was immobilized on MagneGST particles. After incubation, the proteins interacting with GST or GST‐PRSV HC‐Pro were bound to the MagneGST particles. The eluted GST‐bound proteins (lane 4) or GST‐PRSV HC‐Pro‐bound proteins (lane 5) were then analysed by 10% sodium dodecylsulphate‐polyacrylamide gel electrophoresis (SDS‐PAGE) and probed with streptavidin‐alkaline phosphatase (streptavidin‐AP) (A) or anti‐GST antibody (B) (GST, 26.0 kDa; GST‐PRSV HC‐Pro, 78.0 kDa; biotinylated PaCRT, 48.2 kDa). The purified GST (lane 1), purified GST‐PRSV HC‐Pro (lane 2) and in vitro translated biotinylated PaCRT (lane 3) were used as controls, respectively. The <t>prestained</t> dual colour protein size marker (Tiangen) is indicated on the left of the panel.
    Prestained Dual Colour Protein Size Marker, supplied by tiangen biotech co, 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/prestained dual colour protein size marker/product/tiangen biotech co
    Average 86 stars, based on 1 article reviews
    prestained dual colour protein size marker - by Bioz Stars, 2026-03
    86/100 stars
    		  Buy from Supplier

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    In vitro protein‐binding assay of Papaya ringspot virus helper component‐proteinase (PRSV HC‐Pro) and Carica papaya calreticulin (PaCRT). In vitro translated biotinylated PaCRT was incubated with purified glutathione S‐transferase (GST) or GST‐PRSV HC‐Pro, which was immobilized on MagneGST particles. After incubation, the proteins interacting with GST or GST‐PRSV HC‐Pro were bound to the MagneGST particles. The eluted GST‐bound proteins (lane 4) or GST‐PRSV HC‐Pro‐bound proteins (lane 5) were then analysed by 10% sodium dodecylsulphate‐polyacrylamide gel electrophoresis (SDS‐PAGE) and probed with streptavidin‐alkaline phosphatase (streptavidin‐AP) (A) or anti‐GST antibody (B) (GST, 26.0 kDa; GST‐PRSV HC‐Pro, 78.0 kDa; biotinylated PaCRT, 48.2 kDa). The purified GST (lane 1), purified GST‐PRSV HC‐Pro (lane 2) and in vitro translated biotinylated PaCRT (lane 3) were used as controls, respectively. The prestained dual colour protein size marker (Tiangen) is indicated on the left of the panel.

    Journal: Molecular Plant Pathology

    Article Title: Helper component‐proteinase (HC‐Pro) protein of Papaya ringspot virus interacts with papaya calreticulin

    doi: 10.1111/j.1364-3703.2009.00606.x

    Figure Lengend Snippet: In vitro protein‐binding assay of Papaya ringspot virus helper component‐proteinase (PRSV HC‐Pro) and Carica papaya calreticulin (PaCRT). In vitro translated biotinylated PaCRT was incubated with purified glutathione S‐transferase (GST) or GST‐PRSV HC‐Pro, which was immobilized on MagneGST particles. After incubation, the proteins interacting with GST or GST‐PRSV HC‐Pro were bound to the MagneGST particles. The eluted GST‐bound proteins (lane 4) or GST‐PRSV HC‐Pro‐bound proteins (lane 5) were then analysed by 10% sodium dodecylsulphate‐polyacrylamide gel electrophoresis (SDS‐PAGE) and probed with streptavidin‐alkaline phosphatase (streptavidin‐AP) (A) or anti‐GST antibody (B) (GST, 26.0 kDa; GST‐PRSV HC‐Pro, 78.0 kDa; biotinylated PaCRT, 48.2 kDa). The purified GST (lane 1), purified GST‐PRSV HC‐Pro (lane 2) and in vitro translated biotinylated PaCRT (lane 3) were used as controls, respectively. The prestained dual colour protein size marker (Tiangen) is indicated on the left of the panel.

    Article Snippet: The prestained dual colour protein size marker (Tiangen) is indicated on the left of the panel.

    Techniques: In Vitro, Protein Binding, Incubation, Purification, Polyacrylamide Gel Electrophoresis, SDS Page, Marker