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1 kb plus dna ladder  (Thermo Fisher)


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    Structured Review

    Thermo Fisher 1 kb plus dna ladder
    1 Kb Plus Dna Ladder, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 96/100, based on 3145 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/1 kb plus dna ladder/product/Thermo Fisher
    Average 96 stars, based on 3145 article reviews
    1 kb plus dna ladder - by Bioz Stars, 2026-03
    96/100 stars

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    PAGE investigation of CANVAS pathogenic dAGGGA repeats. Migration pattern of dAGGGA repeats and of the reference oligonucleotides d(TGGGTT) n and d(TGGGT) n ( A ) in 100 mM KCl, detected by UV-shadowing; ( B ) in 100 mM KCl, detected by NMM and SYBR Safe staining; ( C ) in 100 mM LiCl, detected by SYBR Safe staining; ( E ) in 100 mM KCl, detected by ThT staining. Strand concentrations: 240/ n μM in gel ( A ), 24/ n μM in gels ( B, C, E ). Electrophoresis of gel ( A ) was carried out at room temperature, whereas gels ( B, C, E ) were run in a cold room. The symbol ”*” marks the major bands detected for d(AGGGA) 4 in gels ( A ) and ( E ) and the d(TGGGT) 8 band in gel ( E ). <t>DNA</t> <t>ladder</t> sizes: 10, 15, 20, 25, 35, 50, 75, 100, 150, 200, 300 bp. Sample buffer: 10 mM cacodylic acid, pH 7.2. ( D ) Schematic representation of the intermolecular G4 and duplex structures formed by d(AGGGA) 8,12,16 corresponding to the gel bands framed by red and blue rectangles, respectively, and schematic representation of putative bimolecular G4s that may be formed by d(AGGGA) 4 .
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    New England Biolabs weight dna ladder
    PAGE investigation of CANVAS pathogenic dAGGGA repeats. Migration pattern of dAGGGA repeats and of the reference oligonucleotides d(TGGGTT) n and d(TGGGT) n ( A ) in 100 mM KCl, detected by UV-shadowing; ( B ) in 100 mM KCl, detected by NMM and SYBR Safe staining; ( C ) in 100 mM LiCl, detected by SYBR Safe staining; ( E ) in 100 mM KCl, detected by ThT staining. Strand concentrations: 240/ n μM in gel ( A ), 24/ n μM in gels ( B, C, E ). Electrophoresis of gel ( A ) was carried out at room temperature, whereas gels ( B, C, E ) were run in a cold room. The symbol ”*” marks the major bands detected for d(AGGGA) 4 in gels ( A ) and ( E ) and the d(TGGGT) 8 band in gel ( E ). <t>DNA</t> <t>ladder</t> sizes: 10, 15, 20, 25, 35, 50, 75, 100, 150, 200, 300 bp. Sample buffer: 10 mM cacodylic acid, pH 7.2. ( D ) Schematic representation of the intermolecular G4 and duplex structures formed by d(AGGGA) 8,12,16 corresponding to the gel bands framed by red and blue rectangles, respectively, and schematic representation of putative bimolecular G4s that may be formed by d(AGGGA) 4 .
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    Image Search Results


    Fluorescently labeled λ-DNA was biotinylated and selectively attached to a glass slide in a flow channel and imaged using high resolution fluorescence microscopy. λ-DNA strands are stretched out under the influence of applied flow and condense to a dense structure under the influence of 1 nM LL-37.

    Journal: bioRxiv

    Article Title: Investigation of Regulation and Binding Patterns of the Human Cathelicidin Peptide LL-37 in Complexation with Nucleic Acids, and its Impact on Neutrophil Extracellular Traps

    doi: 10.64898/2026.02.09.704888

    Figure Lengend Snippet: Fluorescently labeled λ-DNA was biotinylated and selectively attached to a glass slide in a flow channel and imaged using high resolution fluorescence microscopy. λ-DNA strands are stretched out under the influence of applied flow and condense to a dense structure under the influence of 1 nM LL-37.

    Article Snippet: A 1 kb Plus DNA Ladder (New England Biolabs) was substituted with λ DNA to display the migration time of native λ DNA.

    Techniques: Labeling, Fluorescence, Microscopy

    PAGE investigation of CANVAS pathogenic dAGGGA repeats. Migration pattern of dAGGGA repeats and of the reference oligonucleotides d(TGGGTT) n and d(TGGGT) n ( A ) in 100 mM KCl, detected by UV-shadowing; ( B ) in 100 mM KCl, detected by NMM and SYBR Safe staining; ( C ) in 100 mM LiCl, detected by SYBR Safe staining; ( E ) in 100 mM KCl, detected by ThT staining. Strand concentrations: 240/ n μM in gel ( A ), 24/ n μM in gels ( B, C, E ). Electrophoresis of gel ( A ) was carried out at room temperature, whereas gels ( B, C, E ) were run in a cold room. The symbol ”*” marks the major bands detected for d(AGGGA) 4 in gels ( A ) and ( E ) and the d(TGGGT) 8 band in gel ( E ). DNA ladder sizes: 10, 15, 20, 25, 35, 50, 75, 100, 150, 200, 300 bp. Sample buffer: 10 mM cacodylic acid, pH 7.2. ( D ) Schematic representation of the intermolecular G4 and duplex structures formed by d(AGGGA) 8,12,16 corresponding to the gel bands framed by red and blue rectangles, respectively, and schematic representation of putative bimolecular G4s that may be formed by d(AGGGA) 4 .

    Journal: Nucleic Acids Research

    Article Title: Pentanucleotide guanine-rich WGGGW repeats, including CANVAS AGGGA repeats, form a variety of noncanonical structures

    doi: 10.1093/nar/gkag051

    Figure Lengend Snippet: PAGE investigation of CANVAS pathogenic dAGGGA repeats. Migration pattern of dAGGGA repeats and of the reference oligonucleotides d(TGGGTT) n and d(TGGGT) n ( A ) in 100 mM KCl, detected by UV-shadowing; ( B ) in 100 mM KCl, detected by NMM and SYBR Safe staining; ( C ) in 100 mM LiCl, detected by SYBR Safe staining; ( E ) in 100 mM KCl, detected by ThT staining. Strand concentrations: 240/ n μM in gel ( A ), 24/ n μM in gels ( B, C, E ). Electrophoresis of gel ( A ) was carried out at room temperature, whereas gels ( B, C, E ) were run in a cold room. The symbol ”*” marks the major bands detected for d(AGGGA) 4 in gels ( A ) and ( E ) and the d(TGGGT) 8 band in gel ( E ). DNA ladder sizes: 10, 15, 20, 25, 35, 50, 75, 100, 150, 200, 300 bp. Sample buffer: 10 mM cacodylic acid, pH 7.2. ( D ) Schematic representation of the intermolecular G4 and duplex structures formed by d(AGGGA) 8,12,16 corresponding to the gel bands framed by red and blue rectangles, respectively, and schematic representation of putative bimolecular G4s that may be formed by d(AGGGA) 4 .

    Article Snippet: As DNA ladder, we used Thermo ScientificTM GeneRuler Ultra Low Range DNA Ladder, ready-to-use.

    Techniques: Migration, Staining, Electrophoresis