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loading buffer  (Thermo Fisher)


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    Structured Review

    Thermo Fisher loading buffer
    Loading Buffer, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/laemmli+buffer/Laemmli+SDS+sample+buffer%2C+reducing/pmc13315006-219-8-10
    Average 99 stars, based on 1 article reviews
    loading buffer - by Bioz Stars, 2026-09
    99/100 stars

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    Related Articles

    Nucleic Acid Electrophoresis:

    Article Title: Multifaceted regulations of HSV-1 ICP0 on the Anti-Viral Restrictions Imposed by the Host Hippo Kinases Reprogramming
    Article Snippet: .. Total cell lysates were denatured with Laemmli buffer, separated by SDS-polyacrylamide gel electrophoresis and then transferred to a polyvinylidene difluoride (PVDF) membrane (Thermo Scientific, Rockford, IL, USA) or nitrocellulose membrane (Bio-Rad). .. The membrane was blocked with 1× Tris-buffered saline–Tween (TBST) (20 mM Tris, pH7.5, 150 mM NaCl, 0.5% Tween 20) containing 5% nonfat dry milk, and then probed with a primary antibody, rinsed with TBST for three times to react with the horseradish peroxidase-conjugated goat anti-mouse or goat anti-rabbit secondary antibody (Sigma, St. Louis, MO, USA).

    Membrane:

    Article Title: Multifaceted regulations of HSV-1 ICP0 on the Anti-Viral Restrictions Imposed by the Host Hippo Kinases Reprogramming
    Article Snippet: .. Total cell lysates were denatured with Laemmli buffer, separated by SDS-polyacrylamide gel electrophoresis and then transferred to a polyvinylidene difluoride (PVDF) membrane (Thermo Scientific, Rockford, IL, USA) or nitrocellulose membrane (Bio-Rad). .. The membrane was blocked with 1× Tris-buffered saline–Tween (TBST) (20 mM Tris, pH7.5, 150 mM NaCl, 0.5% Tween 20) containing 5% nonfat dry milk, and then probed with a primary antibody, rinsed with TBST for three times to react with the horseradish peroxidase-conjugated goat anti-mouse or goat anti-rabbit secondary antibody (Sigma, St. Louis, MO, USA).

    Article Title: α-Synuclein and γ-Tubulin Cooperatively Regulate Activity-Evoked Presynaptic Microtubule Nucleation to Gate Dopamine Release
    Article Snippet: To determine whether α-synuclein binding in the peptide array assay depends on the presence of the C-terminal tails of α- and/or β-tubulin, regions that harbor most tubulin post-translational modifications, we enzymatically removed these tails using Subtilisin A. Lyophilized porcine tubulin (Cytoskeleton, Cat# T240-B) was resuspended on ice in BRB80 supplemented with 1 mM GTP to a final concentration of 6 mg/ml. .. The tubulin was then incubated with increasing concentrations of Subtilisin A (Sigma-Aldrich, Cat# P5380) at 25°C for 40 min. To assess the extent of C-terminal cleavage, aliquots of the reaction were lysed in Laemmli buffer, resolved on a 10% Bis-Tris gel (Invitrogen), and transferred onto a nitrocellulose membrane. .. The membrane was probed with an antibody against tyrosinated α-tubulin (YL1/2; Sigma-Aldrich, Cat# MAB1864), which recognizes an epitope located within the last few amino acids of the α-tubulin C-terminal tail.

    Incubation:

    Article Title: α-Synuclein and γ-Tubulin Cooperatively Regulate Activity-Evoked Presynaptic Microtubule Nucleation to Gate Dopamine Release
    Article Snippet: To determine whether α-synuclein binding in the peptide array assay depends on the presence of the C-terminal tails of α- and/or β-tubulin, regions that harbor most tubulin post-translational modifications, we enzymatically removed these tails using Subtilisin A. Lyophilized porcine tubulin (Cytoskeleton, Cat# T240-B) was resuspended on ice in BRB80 supplemented with 1 mM GTP to a final concentration of 6 mg/ml. .. The tubulin was then incubated with increasing concentrations of Subtilisin A (Sigma-Aldrich, Cat# P5380) at 25°C for 40 min. To assess the extent of C-terminal cleavage, aliquots of the reaction were lysed in Laemmli buffer, resolved on a 10% Bis-Tris gel (Invitrogen), and transferred onto a nitrocellulose membrane. .. The membrane was probed with an antibody against tyrosinated α-tubulin (YL1/2; Sigma-Aldrich, Cat# MAB1864), which recognizes an epitope located within the last few amino acids of the α-tubulin C-terminal tail.

    SDS Page:

    Article Title: ATML1-GIR1-TPL/TPR transcriptional repression module controls glucosinolates and giant cells in Arabidopsis thaliana sepals
    Article Snippet: .. Beads were eluted in 100 μL Laemmli buffer and resolved by SDS-PAGE followed by western blot with rabbit anti-GFP (1:2000, Invitrogen, A-11122) or rat anti-HA (1:5000, Roche, 11867431001) primary antibodies and goat anti-rabbit (1:2000; Enzo, ADI-SAB-300) or anti-rat (1:3000; Millipore, AP136P) secondary antibodies. .. SuperSignal West Femto Maximum Sensitivity Substrate (ThermoFisher Scientific) was used for chemiluminescent detection with an Azure c300 imager (Azure Biosystems).

    Article Title: Physicochemical stability and protein corona profiling on the interaction of iron oxide nanoparticles with human tears.
    Article Snippet: .. SDS-PAGE of tear extract controls and unbound or loosely bound (soft corona) proteins and the IONP extracted proteins, 10 mL of each protein samples were mixed separately with 10 mL of 2 Laemmli buffer (Invitrogen) and heated at 95 1C for 5 minutes to ensure complete protein denaturation. .. The prepared samples, along with 2 mL of Benchmarkt pre-stained protein molecular weight ladder (Invitrogen), were loaded onto a 12% Tris-polyacrylamide gel and electrophoresed in Trisglycine running buffer (Invitrogen) at 120 V for 45 minutes.

    Western Blot:

    Article Title: ATML1-GIR1-TPL/TPR transcriptional repression module controls glucosinolates and giant cells in Arabidopsis thaliana sepals
    Article Snippet: .. Beads were eluted in 100 μL Laemmli buffer and resolved by SDS-PAGE followed by western blot with rabbit anti-GFP (1:2000, Invitrogen, A-11122) or rat anti-HA (1:5000, Roche, 11867431001) primary antibodies and goat anti-rabbit (1:2000; Enzo, ADI-SAB-300) or anti-rat (1:3000; Millipore, AP136P) secondary antibodies. .. SuperSignal West Femto Maximum Sensitivity Substrate (ThermoFisher Scientific) was used for chemiluminescent detection with an Azure c300 imager (Azure Biosystems).

    Protease Inhibitor:

    Article Title: Immortalization of human airway epithelial cells for genome editing applications
    Article Snippet: .. Differentiated cells were trypsinized and lysed in Laemmli buffer (120 mM Tris-HCl pH 6.8, 20 % glycerol, 4 % sodium dodecyl sulfate (SDS), protease inhibitor (Fisher Emergo B.V.)), and the lysates were homogenized using a QIAshredder (QIAGEN N.V., Germany) column to reduce viscosity. .. Protein concentration was measured using the Pierce BCA Protein Assay Kit (Thermo Fisher Scientific, MA, USA) according to the manufacturer’s instructions.

    Viscosity:

    Article Title: Immortalization of human airway epithelial cells for genome editing applications
    Article Snippet: .. Differentiated cells were trypsinized and lysed in Laemmli buffer (120 mM Tris-HCl pH 6.8, 20 % glycerol, 4 % sodium dodecyl sulfate (SDS), protease inhibitor (Fisher Emergo B.V.)), and the lysates were homogenized using a QIAshredder (QIAGEN N.V., Germany) column to reduce viscosity. .. Protein concentration was measured using the Pierce BCA Protein Assay Kit (Thermo Fisher Scientific, MA, USA) according to the manufacturer’s instructions.

    Protein Concentration:

    Article Title: A novel ψ–χ fusion protein for unravelling the contributions of χ to DNA replication and repair
    Article Snippet: Cell pellets were lysed using NEBExpress E. coli Lysis Reagent (New England Biolabs) at 5 ml g −1 of cell mass and incubated at room temperature for 20 min, with inversions every 2 min. Lysates were centrifuged at 4°C, separating supernatant and pellet fractions. .. Protein concentration in supernatant fractions was measured at 280 nm using a NanoDrop spectrophotometer and normalized to 5.3 mg ml −1 using lysis reagent and Laemmli buffer. ..

    Spectrophotometry:

    Article Title: A novel ψ–χ fusion protein for unravelling the contributions of χ to DNA replication and repair
    Article Snippet: Cell pellets were lysed using NEBExpress E. coli Lysis Reagent (New England Biolabs) at 5 ml g −1 of cell mass and incubated at room temperature for 20 min, with inversions every 2 min. Lysates were centrifuged at 4°C, separating supernatant and pellet fractions. .. Protein concentration in supernatant fractions was measured at 280 nm using a NanoDrop spectrophotometer and normalized to 5.3 mg ml −1 using lysis reagent and Laemmli buffer. ..

    Lysis:

    Article Title: A novel ψ–χ fusion protein for unravelling the contributions of χ to DNA replication and repair
    Article Snippet: Cell pellets were lysed using NEBExpress E. coli Lysis Reagent (New England Biolabs) at 5 ml g −1 of cell mass and incubated at room temperature for 20 min, with inversions every 2 min. Lysates were centrifuged at 4°C, separating supernatant and pellet fractions. .. Protein concentration in supernatant fractions was measured at 280 nm using a NanoDrop spectrophotometer and normalized to 5.3 mg ml −1 using lysis reagent and Laemmli buffer. ..



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