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Rs23910

Manufactured by Immunoway
Sourced in United States

The RS23910 is a laboratory equipment designed for general experimental purposes. It is a multi-purpose device that can be utilized in various scientific applications. The core function of the RS23910 is to perform tasks related to sample preparation, analysis, and data collection. Further details about the specific intended use or capabilities of this product are not available.

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3 protocols using rs23910

1

Protein Expression Analysis by Western Blot

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Total protein was extracted from the cells using 1 × RIPA lysis buffer (P10013B, Beyotime, Shanghai, China). The concentration of protein was measured by using BCA Protein Assay Kit (P0010, Beyotime, Shanghai, China). And then equal amounts of proteins were separated by SDS-PAGE and transferred to nitrocellulose filter membrane (NC membrane). After electroblotting, the membranes were blocked with PBS-5% fat-free dried milk at room temperature for 1 h and incubated with primary antibodies for LDHA (1:2000, Santa Cruz sc-137243, Texas, USA), PFKM (1:1000, ABclonal A5477, Shanghai, China), NAT10 (1:1000, ABclonal A19286, Wuhan, China), YTHDC1 (1:500, Proteintech 14,392–1-AP, Wuhan, China), ac4C (1:1000, Abcam ab253039, Cambridge, UK) or β-actin (1:5000, Abcam ab253039, Cambridge, UK). The membrane was then incubated with anti-mouse secondary antibodies (RS23910, ImmunoWay, USA) or anti-rabbit secondary antibodies (RS23920, ImmunoWay, USA). Results were detected using Odessey Clex (LI-COR, USA), followed by further analysis.
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2

Protein Expression Analysis via Western Blot

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The total proteins were extracted from cells or tissues using 1 × RIPA lysis buffer supplemented with a protease inhibitor cocktail (Roche). The concentrations of extracted total protein samples were measured by a BCA Protein Assay Kit (Beyotime). Equal amounts of proteins were separated by SDS-PAGE and transferred to nitrocellulose filter membranes. After blocking the membranes with non-fat milk (5% w/v) for 1 h, the proteins were incubated at 4 °C overnight with the primary antibodies against CD63 (1:1,000, WL02549, Wanleibio, China), CD81 (1:1,500, GTX101768, Gene Tex, USA), TSG101 (1:1,500, GTX70255, Gene Tex), ACSL4 (1:10,000, ab155282, Abcam, UK), GPX4 (1:1,000, A13309, Abclonal, USA), GAPDH (1:5,000, AC002, Abclonal), or β-Tubulin (1:5,000, AC021, Abclonal). Next, the membranes were incubated with secondary anti-mouse or anti-rabbit antibodies (RS23910 and RS23920, ImmunoWay, USA) in dark at room temperature for 1 h. The membranes were scanned, and the gray values of protein band were detected by Odessey CLx (LI-COR, USA).
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3

Western Blot Analysis of Protein Targets

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Cell samples were washed using PBS, and then the total proteins were extracted using 1×RIPA lysis buffer (Beyotime, Shanghai, China). The lysates were fully crushed by ultrasonic and cleared by high-speed centrifugation at 13,500g for 15 min. The extracted total proteins were quanti ed by BCA Protein Assay Kit (Beyotime, Shanghai, China), then equal amounts of proteins were separated by SDS-PAGE and transferred to NC membrane. After the membranes were blocked with 5% w/v non-fat milk for 1h, the proteins were probed at 4℃ overnight using different primary antibodies METTL1 (14994-1-AP, proteintech), FTH1 (#4393, CST), GPX4 (A13309, Abclonal), GAPDH (AC002, Abclonal), β-Tubulin (AC021, Abclonal). On the next day, the membranes were incubated with a secondary antibody (RS23910, ImmunoWay) for 1 h at room temperature. Results were detected using Odessey Clex (LI-COR, America), followed by further analysis.
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