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6x native gel loading buffer  (Bio-Rad)


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    Structured Review

    Bio-Rad 6x native gel loading buffer
    6x Native Gel Loading Buffer, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 96/100, based on 1968 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/5%C3%97native+sample+loading+buffer/Bromophenol+Blue/pm40603872-377-6-45
    Average 96 stars, based on 1968 article reviews
    6x native gel loading buffer - by Bioz Stars, 2026-11
    96/100 stars

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    Related Articles

    Centrifugation:

    Article Title: Cadmium impairs heart ventricular formation and disrupts polysialylated-NCAM/FGF receptor signaling in Xenopus tadpoles.
    Article Snippet: For subcellular analysis, oocytes were manually enucleated (30 nuclei/10 μL in PYT buffer), their cytoplasm aspirated using a positive displacement digital micropipette (Nichiryo) (30 cytoplasm/150 μL PYT buffer), and the membrane and resuspended in PYT (30 membrane/50 μL PYT) before they were homogenized in a glass grinder at 4 °C. .. After a 12000 g centrifugation for 10 min at 4 °C, the supernatants were denaturated in 2X Laëmmli buffer (65.8 mM Tris-HCl pH 6.8; 26.3 % (v/v) glycerol; 2.1 % (m/v) SDS; 0.01 % (m/v) bromophenol blue; 4% (v/v) β-mercaptoethanol, BioRad) for 3 min at 96 °C or at 60 °C for PSA analysis. .. Protein concentration of supernatants was determined and adjusted if necessary, using BioRad assay at 595 nm (SPECTROstar Nano, BMG LABTECH) and adjusted if necessary.

    Article Title: Generation of a recombinant, antibiotic resistance gene-free Leishmania tarentolae strain as a live vaccine platform
    Article Snippet: .. The resulting pellet was resuspended in 6x SDS-PAGE sample buffer (4.5 mM Tris–HCl (pH 6.8), 10% v/v glycerol, 2% w/v SDS, 5% v/v 2-mercaptoethanol, 0.05% w/v bromophenol blue) and boiled for 5 min. After a brief centrifugation, the supernatants were loaded onto a 15% SDSPAGE polyacrylamide gel (Bio-Rad). .. Proteins were then transferred to a nitrocellulose membrane (Schleicher and Schuell Bioscience, Dassel, Germany).

    Western Blot:

    Article Title: Spatiotemporal expression and hormonal regulation of antioxidant enzymes in the bovine oviduct epithelium.
    Article Snippet: .. Oviduct flushing samples were collected as previously described and directly lysed by resuspension in 4X Laemmli buffer [250 mM Tris pH 6.8, 40% glycerol, 8% sodium dodecyl sulfate (SDS), 20% Tris(2carboxyethyl)phosphine (TCEP), bromophenol blue], followed by boiling at 100◦C for 4 min. For Western Blotting, 30 μg of proteins were migrated on a 4%–20% SDS-PAGE gel (Bio-Rad, Hercules, CA, USA), and semi-liquid transfers were performed on a nitrocellulose membrane with the Trans-blot Turbo Transfer System (Bio-Rad) using the “Mixed molecular weight” program. ..

    SDS Page:

    Article Title: Spatiotemporal expression and hormonal regulation of antioxidant enzymes in the bovine oviduct epithelium.
    Article Snippet: .. Oviduct flushing samples were collected as previously described and directly lysed by resuspension in 4X Laemmli buffer [250 mM Tris pH 6.8, 40% glycerol, 8% sodium dodecyl sulfate (SDS), 20% Tris(2carboxyethyl)phosphine (TCEP), bromophenol blue], followed by boiling at 100◦C for 4 min. For Western Blotting, 30 μg of proteins were migrated on a 4%–20% SDS-PAGE gel (Bio-Rad, Hercules, CA, USA), and semi-liquid transfers were performed on a nitrocellulose membrane with the Trans-blot Turbo Transfer System (Bio-Rad) using the “Mixed molecular weight” program. ..

    Article Title: Generation of a recombinant, antibiotic resistance gene-free Leishmania tarentolae strain as a live vaccine platform
    Article Snippet: .. The resulting pellet was resuspended in 6x SDS-PAGE sample buffer (4.5 mM Tris–HCl (pH 6.8), 10% v/v glycerol, 2% w/v SDS, 5% v/v 2-mercaptoethanol, 0.05% w/v bromophenol blue) and boiled for 5 min. After a brief centrifugation, the supernatants were loaded onto a 15% SDSPAGE polyacrylamide gel (Bio-Rad). .. Proteins were then transferred to a nitrocellulose membrane (Schleicher and Schuell Bioscience, Dassel, Germany).

    Membrane:

    Article Title: Spatiotemporal expression and hormonal regulation of antioxidant enzymes in the bovine oviduct epithelium.
    Article Snippet: .. Oviduct flushing samples were collected as previously described and directly lysed by resuspension in 4X Laemmli buffer [250 mM Tris pH 6.8, 40% glycerol, 8% sodium dodecyl sulfate (SDS), 20% Tris(2carboxyethyl)phosphine (TCEP), bromophenol blue], followed by boiling at 100◦C for 4 min. For Western Blotting, 30 μg of proteins were migrated on a 4%–20% SDS-PAGE gel (Bio-Rad, Hercules, CA, USA), and semi-liquid transfers were performed on a nitrocellulose membrane with the Trans-blot Turbo Transfer System (Bio-Rad) using the “Mixed molecular weight” program. ..

    Molecular Weight:

    Article Title: Spatiotemporal expression and hormonal regulation of antioxidant enzymes in the bovine oviduct epithelium.
    Article Snippet: .. Oviduct flushing samples were collected as previously described and directly lysed by resuspension in 4X Laemmli buffer [250 mM Tris pH 6.8, 40% glycerol, 8% sodium dodecyl sulfate (SDS), 20% Tris(2carboxyethyl)phosphine (TCEP), bromophenol blue], followed by boiling at 100◦C for 4 min. For Western Blotting, 30 μg of proteins were migrated on a 4%–20% SDS-PAGE gel (Bio-Rad, Hercules, CA, USA), and semi-liquid transfers were performed on a nitrocellulose membrane with the Trans-blot Turbo Transfer System (Bio-Rad) using the “Mixed molecular weight” program. ..

    other:

    Article Title: Immune-Complex-Based In Vitro Deubiquitination Assay
    Article Snippet: Bromophenol blue (Bio-Rad, catalog number: 1610404) 38.

    Article Title: In silico screening, synthesis, and biological evaluation of pyrazolopyrimidine-derived mTOR inhibitors for anticancer and senomorphic effects.
    Article Snippet: For immunoblotting, the following primary and secondary antibodies were used: rabbit polyclonal p70 S6 kinase (#9202), rabbit monoclonal phosphop70 S6 kinase (Thr389) (#9234), rabbit monoclonal AKT kinase (#4691), rabbit monoclonal phospho-AKT kinase (Ser473) (#4060), rabbit monoclonal LC3B (#3868), mouse monoclonal p62/SQSTM1 (#88588) obtained from Cell Signaling Technology, Inc., Danvers, MA, USA; mouse monoclonal LAMP2 (555803) BD Pharmingen, Inc., San Diego, CA, USA; and mouse monoclonal anti-GAPDH (GTX3066) purchased from GeneTex, Inc., Irvine, CA, USA; goat anti-mouse (170-6516) or anti-rabbit IgG (H + L)-HRP conjugate (170-6515) purchased from BioRad, Hercules, CA, USA.

    Staining:

    Article Title: A Minimal Synthetic IAA Pathway in Escherichia coli Using Avocado Seed Hydrolysate: A Sustainable and Didactic Platform for Synthetic Biology
    Article Snippet: .. The gels were run until the bromophenol blue dye front reached the bottom of the gel, then stained with Coomassie Brilliant Blue (Bio-Rad, Hercules, CA, USA) and destained to visualize the separated proteins. ..

    Incubation:

    Article Title: VISTA drives tumour-intrinsic proliferation in mesothelioma cells.
    Article Snippet: BACKGROUND: Mesothelioma is a therapeutic challenge because current therapies have limited efficacy.. In this study, we investigated the role of the immune checkpoint molecule V-domain Ig suppressor of T cell activation (VISTA) in mesothelioma cells.. METHODS: The effect of VISTA expression on cell proliferation was analysed using mesothelioma cell lines and a mouse xenograft model. To investigate the underlying mechanisms, we performed immunoprecipitation–mass spectrometry and RNA-seq analysis to identify VISTA-associated proteins and downstream transcriptional changes.

    Polyacrylamide Gel Electrophoresis:

    Article Title: VISTA drives tumour-intrinsic proliferation in mesothelioma cells.
    Article Snippet: BACKGROUND: Mesothelioma is a therapeutic challenge because current therapies have limited efficacy.. In this study, we investigated the role of the immune checkpoint molecule V-domain Ig suppressor of T cell activation (VISTA) in mesothelioma cells.. METHODS: The effect of VISTA expression on cell proliferation was analysed using mesothelioma cell lines and a mouse xenograft model. To investigate the underlying mechanisms, we performed immunoprecipitation–mass spectrometry and RNA-seq analysis to identify VISTA-associated proteins and downstream transcriptional changes.



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