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6x blue gel loading dye  (New England Biolabs)


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    Structured Review

    New England Biolabs 6x blue gel loading dye
    6x Blue Gel Loading Dye, supplied by New England Biolabs, used in various techniques. Bioz Stars score: 95/100, based on 221 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/6x+blue+gel+loading+dye/Gel+Loading+Dye%2C+Blue/pm41986708-614-7-12
    Average 95 stars, based on 221 article reviews
    6x blue gel loading dye - by Bioz Stars, 2026-10
    95/100 stars

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    Related Articles

    Incubation:

    Article Title: Beta2-containing nicotinic acetylcholine receptors mediate calcium/calmodulin-dependent protein kinase-II and synapsin I protein levels in the nucleus accumbens after nicotine withdrawal in mice
    Article Snippet: .. 30 μg of protein were incubated with 6X blue gel loading dye (New England Biolabs, Ipswich, MA, USA), and heated for 5 minutes at 95°C. ..

    Article Title: Association of the histidine-triad nucleotide-binding protein-1 ( HINT1 ) gene variants with nicotine dependence
    Article Snippet: .. Protein concentrations were determined using the Bradford assay and 30 μg of protein were incubated with 6X blue gel loading dye (New England Biolabs, Ipswich, MA, USA) and heated for 5 min at 95 °C. ..

    Article Title: Nicotine Reward and Affective Nicotine Withdrawal Signs Are Attenuated in Calcium/Calmodulin-Dependent Protein Kinase IV Knockout Mice
    Article Snippet: .. 30 μg of protein were incubated with 6X blue gel loading dye (New England Biolabs, Ipswich, MA, USA), and heated for 5 minutes at 95°C. ..

    SDS Page:

    Article Title: The Inhibitory Effect of Non-Substrate and Substrate DNA on the Ligation and Self-Adenylylation Reactions Catalyzed by T4 DNA Ligase.
    Article Snippet: .. The flow-through was mixed with 8 μL of 6X Blue Gel Loading Dye (New England Biolabs), and 20-μL aliquots were loaded onto (4–20%) Tris Glycine SDS-PAGE gels and run at 120 V for 30 minutes. .. The gels were Coomassie stained, the protein band was cut out, and the amount of 32P-AMP incorporation was counted on a Tri-carb 2900TR liquid scintillation counter (Perkin Elmer, Waltham, MA).

    Article Title: The Inhibitory Effect of Non-Substrate and Substrate DNA on the Ligation and Self-Adenylylation Reactions Catalyzed by T4 DNA Ligase
    Article Snippet: .. The flow-through was mixed with 8 μL of 6X Blue Gel Loading Dye (New England Biolabs), and 20-μL aliquots were loaded onto (4–20%) Tris Glycine SDS-PAGE gels and run at 120 V for 30 minutes. .. The gels were Coomassie stained, the protein band was cut out, and the amount of 32 P-AMP incorporation was counted on a Tri-carb 2900TR liquid scintillation counter (Perkin Elmer, Waltham, MA).

    Bradford Assay:

    Article Title: Association of the histidine-triad nucleotide-binding protein-1 ( HINT1 ) gene variants with nicotine dependence
    Article Snippet: .. Protein concentrations were determined using the Bradford assay and 30 μg of protein were incubated with 6X blue gel loading dye (New England Biolabs, Ipswich, MA, USA) and heated for 5 min at 95 °C. ..

    Polymerase Chain Reaction:

    Article Title: Molecular basis for methylation-sensitive editing by Cas9.
    Article Snippet: For PCR amplification, 1 μl of the reaction product was mixed with 0.25–1 μM primers and Q5 High-Fidelity 2X Master Mix (New England Biolabs). .. The PCR product was then mixed with 6X blue gel loading dye (New England Biolabs) and loaded onto a 2% agarose gel with a 100-bp DNA ladder (New England Biolabs) for electrophoresis. ..

    Agarose Gel Electrophoresis:

    Article Title: Molecular basis for methylation-sensitive editing by Cas9.
    Article Snippet: For PCR amplification, 1 μl of the reaction product was mixed with 0.25–1 μM primers and Q5 High-Fidelity 2X Master Mix (New England Biolabs). .. The PCR product was then mixed with 6X blue gel loading dye (New England Biolabs) and loaded onto a 2% agarose gel with a 100-bp DNA ladder (New England Biolabs) for electrophoresis. ..

    Electrophoresis:

    Article Title: Molecular basis for methylation-sensitive editing by Cas9.
    Article Snippet: For PCR amplification, 1 μl of the reaction product was mixed with 0.25–1 μM primers and Q5 High-Fidelity 2X Master Mix (New England Biolabs). .. The PCR product was then mixed with 6X blue gel loading dye (New England Biolabs) and loaded onto a 2% agarose gel with a 100-bp DNA ladder (New England Biolabs) for electrophoresis. ..



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