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Anti slc3a2

Manufactured by Santa Cruz Biotechnology

Anti-SLC3A2 is a primary antibody that recognizes the SLC3A2 protein. SLC3A2 is a component of the system L amino acid transporter complex, which is responsible for the transport of large neutral amino acids across the cell membrane. The anti-SLC3A2 antibody can be used to detect and study the expression and localization of the SLC3A2 protein in various biological samples.

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2 protocols using anti slc3a2

1

Western Blot Analysis of Protein Markers

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Samples from tissues or cells were lysed in RIPA buffer supplemented with 1x protease and phosphatase inhibitor cocktail (Thermo Fisher, America) and incubated on ice for 30 min. After centrifugation at 14000 × g for 10 min at 4 °C, the supernatant was collected to determine the protein concentration by BCA assay. The samples were prepared for electrophoresis, followed by transfer onto PVDF membranes. The primary antibodies used in this work were as follows: anti-ZO-1 (Santa Cruz Biotechnology), anti-p-MLKL (Cell Signaling Technology), anti-p-RIP1 (Cell Signaling Technology), anti-cleaved/full-length caspase 9 (Cell Signaling Technology), anti-cleaved/full-length caspase 3 (Cell Signaling Technology), anti-GPX4 (Santa Cruz Biotechnology), anti-SLC3A2 (Santa Cruz Biotechnology), anti-SLC7A11 (Santa Cruz Biotechnology), anti-ANXA2 (ABclonal), anti-His-tag (ABclonal), anti-HA-tag (ABclonal), anti-HSPB1 (Cell Signaling Technology), and anti-PRDX1 (Cell Signaling Technology). Secondary antibodies were purchased from ABclonal. The membranes were visualized via the chemiluminescence method.
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2

Protein Expression Analysis of Xenograft Tissues

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50 mg of xenograft tissues were homogenized and lysed using RIPA lysis buffer containing protease inhibitor cocktails (Thermo Scientific). Protein was quantified using the BCA assay, and an equal amount of protein for each lysate (50 ug) was resolved by 4–12% gradient SDS-PAGE followed by transfer onto nitrocellulose membranes. Membranes were blocked with 5% milk for 1 hour in tris buffered saline and probed with primary antibodies for overnight at 4° C in tris buffered saline. Washing was followed by incubation with secondary antibody for 1 hour at room temperature in tris buffered saline containing 0.1% Tween-20. Anti-GPX4 (sc-166120, 1:1000 for WB) and anti-GAPDH antibodies (sc-32233, 1:3000) were obtained from Santa Cruz Biotechnology. Anti-SLC7A11 antibody was purchased from Invitrogen, Thermo Fisher Scientific (PA1-16775, 1:500 for WB). Anti-SLC3A2 was purchased from Santa Cruz (sc-376815). Secondary antibodies with HRP were obtained from Fisher Scientific (anti-mouse PI31432, and anti-rabbit PI31462, 1:2000). Pierce ECL Western Blotting Substrate (Thermo Fisher Scientific, PI32106) was used to develop chemiluminescent signals that were measured on an IVIS Lumina imager.
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