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5 end tag dna rna labeling kit  (Vector Laboratories)


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    Vector Laboratories 5 end tag dna rna labeling kit
    5 End Tag Dna Rna Labeling Kit, supplied by Vector Laboratories, used in various techniques. Bioz Stars score: 94/100, based on 51 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/5 end tag dna rna labeling kit/product/Vector Laboratories
    Average 94 stars, based on 51 article reviews
    5 end tag dna rna labeling kit - by Bioz Stars, 2026-01
    94/100 stars

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    dna end tag kit  (Vector Laboratories)
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    ( A ) 80S complexes (with yeast ribosomes) were assembled <t>on</t> <t>IRES</t> (Cy3) molecules (hybridized to a biotinylated <t>DNA)</t> that were tethered to microscope slide surfaces coated with polyethylene glycol (PEG)-Biotin via a streptavidin bridge. In the cartoon shown here, the wild-type IRES has undergone the first pseudotranslocation event so that domain 3 sits at the P site and the Phe-tRNA Phe (Cy5) is delivered to the A site by eEF1A (tRNA from Escherichia coli ), thereby generating a surface-tethered complex with spatially colocalized Cy3 and Cy5 spots. Sample Cy3 and Cy5 frames from an experiment in which Phe-tRNA Phe (Cy5) was delivered as a ternary complex with eEF1A and GTP, to yeast 80S complexes assembled on WT Cricket Paralysis Virus (CrPV) IRES (Cy3), are depicted in ( B ) and ( C ), respectively. The imaged Cy3 and Cy5 spots in these frames are false colored as green and red, respectively. ( D ) Superposition of the two frames in which regions that appear to have colocalized green and red spots, just by manual inspection, are false colored as yellow for visual clarity; the actual analysis of the extent of colocalization involves a much more rigorous mathematical treatment of the raw data using home-built codes. The panels below ( B )–( D ) show a representative region from the corresponding frames, magnified 6x, to demonstrate the well-resolved distribution of spots and the precision of colocalization. ( E ) Identical images as ( B – D ), except in the presence of eEF2, which results in higher levels of colocalization. DOI: http://dx.doi.org/10.7554/eLife.08146.020
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    ( A ) 80S complexes (with yeast ribosomes) were assembled on IRES (Cy3) molecules (hybridized to a biotinylated DNA) that were tethered to microscope slide surfaces coated with polyethylene glycol (PEG)-Biotin via a streptavidin bridge. In the cartoon shown here, the wild-type IRES has undergone the first pseudotranslocation event so that domain 3 sits at the P site and the Phe-tRNA Phe (Cy5) is delivered to the A site by eEF1A (tRNA from Escherichia coli ), thereby generating a surface-tethered complex with spatially colocalized Cy3 and Cy5 spots. Sample Cy3 and Cy5 frames from an experiment in which Phe-tRNA Phe (Cy5) was delivered as a ternary complex with eEF1A and GTP, to yeast 80S complexes assembled on WT Cricket Paralysis Virus (CrPV) IRES (Cy3), are depicted in ( B ) and ( C ), respectively. The imaged Cy3 and Cy5 spots in these frames are false colored as green and red, respectively. ( D ) Superposition of the two frames in which regions that appear to have colocalized green and red spots, just by manual inspection, are false colored as yellow for visual clarity; the actual analysis of the extent of colocalization involves a much more rigorous mathematical treatment of the raw data using home-built codes. The panels below ( B )–( D ) show a representative region from the corresponding frames, magnified 6x, to demonstrate the well-resolved distribution of spots and the precision of colocalization. ( E ) Identical images as ( B – D ), except in the presence of eEF2, which results in higher levels of colocalization. DOI: http://dx.doi.org/10.7554/eLife.08146.020

    Journal: eLife

    Article Title: A dynamic RNA loop in an IRES affects multiple steps of elongation factor-mediated translation initiation

    doi: 10.7554/eLife.08146

    Figure Lengend Snippet: ( A ) 80S complexes (with yeast ribosomes) were assembled on IRES (Cy3) molecules (hybridized to a biotinylated DNA) that were tethered to microscope slide surfaces coated with polyethylene glycol (PEG)-Biotin via a streptavidin bridge. In the cartoon shown here, the wild-type IRES has undergone the first pseudotranslocation event so that domain 3 sits at the P site and the Phe-tRNA Phe (Cy5) is delivered to the A site by eEF1A (tRNA from Escherichia coli ), thereby generating a surface-tethered complex with spatially colocalized Cy3 and Cy5 spots. Sample Cy3 and Cy5 frames from an experiment in which Phe-tRNA Phe (Cy5) was delivered as a ternary complex with eEF1A and GTP, to yeast 80S complexes assembled on WT Cricket Paralysis Virus (CrPV) IRES (Cy3), are depicted in ( B ) and ( C ), respectively. The imaged Cy3 and Cy5 spots in these frames are false colored as green and red, respectively. ( D ) Superposition of the two frames in which regions that appear to have colocalized green and red spots, just by manual inspection, are false colored as yellow for visual clarity; the actual analysis of the extent of colocalization involves a much more rigorous mathematical treatment of the raw data using home-built codes. The panels below ( B )–( D ) show a representative region from the corresponding frames, magnified 6x, to demonstrate the well-resolved distribution of spots and the precision of colocalization. ( E ) Identical images as ( B – D ), except in the presence of eEF2, which results in higher levels of colocalization. DOI: http://dx.doi.org/10.7554/eLife.08146.020

    Article Snippet: IRES RNAs were labeled using Cy3-maleimide (GE Healthcare) and the 3’ DNA End-Tag Kit (Vector Labs, Burlingame, CA), which added one additional dG residue harboring the Cy3 label to the 3’ end of the IRES construct.

    Techniques: Microscopy