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Nupage 4 to 12 gradient bis tris polyacrylamide protein gels

Manufactured by Thermo Fisher Scientific

The NuPAGE 4 to 12% gradient Bis-Tris polyacrylamide protein gels are used for the separation and analysis of proteins based on their molecular weight. The gels provide a gradient of polyacrylamide concentrations, allowing for the effective separation of a wide range of protein sizes in a single electrophoresis run.

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2 protocols using nupage 4 to 12 gradient bis tris polyacrylamide protein gels

1

Western Blot Analysis of Frozen Samples

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Frozen brain samples were transferred into ice-cold radioimmunoprecipitation assay (RIPA) buffer (Santa Cruz) – containing protease inhibitors, phenylmethylsulfonyl fluoride, and sodium orthovanadate –, homogenized with a polytron, and spun down twice for 20 min at 13000 rpm at 4 °C to remove cell debris. Protein concentration was quantified using a bicinchoninic acid assay (Pierce BCA protein assay kit, Thermo Fisher Scientific) according to the manufacturer’s instruction. Equal amounts of protein (20 μg per lane) were loaded, and electrophoresis was performed in NuPAGE 4 to 12% gradient Bis-Tris polyacrylamide protein gels (Thermo Fisher Scientific). Transfer was performed using PVDF membranes with the Biorad wet transfer system (Bio-Rad Laboratories). Membranes were blocked with 5% milk in PBS with 0.1% Tween-20 (Sigma Aldrich), incubated overnight with primary antibodies (Table S3) at 4°C, washed, and incubated with secondary antibody for 2 h at room temperature. After a final wash, secondary antibodies were visualized using Pierce ECL chemiluminescence reagents (Thermo Fisher Scientific) and the signal was captured with X-ray films (Thomas Scientific).
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2

Western Blot Protein Quantification

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Total protein was extracted using RIPA buffer (Boston Bioproducts) supplemented with Complete, Mini, EDTA-free Protease Inhibitor Cocktail (Millipore Sigma). Protein concentrations were determined using the Micro BCA Protein Assay Kit (Thermo Fisher Scientific). Equal amounts of protein were loaded, and electrophoresis was performed in NuPAGE 4 to 12% gradient Bis-Tris polyacrylamide protein gels (Thermo Fisher Scientific). Proteins were transferred to Immun-Blot PVDF membranes (Bio-Rad) and then blocked with 5% milk in tris-buffered saline with 0.1% Tween (TBS-T, Boston Bioproduct) for 1 h. Membranes were incubated overnight with primary antibodies at 4°C. Blots were washed and incubated with secondary antibodies for 2 h at room temperature. After washing, bands were visualized with ECL chemiluminescence reagents (Genesee Scientific) using the iBright Imaging System (Thermo Fisher Scientific). Band intensity was measured using the Image Studio Lite software (LI-COR Biosciences). Protein expression level was normalized to β-actin or total Tau as appropriate. Antibodies and other key resources are listed in Table S9.
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