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Snail antibody

Manufactured by Abcam
Sourced in United States

The Snail antibody is a primary antibody used for the detection and analysis of the Snail protein, a transcriptional regulator involved in the epithelial-mesenchymal transition process. This antibody can be used in various research applications, such as Western blotting, immunohistochemistry, and immunocytochemistry, to study the expression and localization of the Snail protein in biological samples.

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4 protocols using snail antibody

1

Western Blot Analysis of EMT Pathway

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Western blot was carried out according as described [41 (link), 42 (link)] with rabbit polyclonal PLOD2, E-cadherin and β-catenin antibodies (1:1000; Proteintech, USA), PI3K, p-PI3K (Tyr458), AKT, p-AKT (Ser473), GSK-3β, p-GSK-3β, N-Cadherin, Slug and Vimentin antibodies (1:1000; Cell Signaling Technology, Danvers, MA, USA), as well as Snail antibody (1:1000; Abcam, USA). Mouse monoclonal HIF-1α antibody (1:50; Novus Biologicals, USA) was used for normalization. An HRP-conjugated anti-rabbit or anti-mouse IgG antibody was used as the secondary antibody (1:2000; CoWin Bioscience, Beijing, China). Signals were detected using enhanced chemiluminescence reagents (Pierce, Rockford, IL, USA).
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2

Regulation of EMT by GROα in Tumor Cells

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Materials were purchased from various manufacturers: recombinant GROα (R&D Systems), GROα siRNA (Santa Cruz Biotechnology), control siRNA (Santa Cruz Biotechnology), Lipofectamine ltx (Invitrogen), Opti-MEM Reduced Serum medium (Invitrogen), GROα ELISA kit (R&D Systems), GROα primers (IDT), ThermoScript™ RT-PCR systems (Invitrogen), SYBR Green (Qiagen), EMT marker primers (IDT), PD98059 (Cell Signaling), E-cadherin antibody (Santa Cruz Biotechnology), N-cadherin antibody (Santa Cruz Biotechnology), Snail antibody (Abcam), Slug antibody (Abcam), Twist antibody (Santa Cruz Biotechnology), Vimentin antibody (Santa Cruz Biotechnology), VEGF antibody (Santa Cruz Biotechnology), phospho-MAPK antibody (Cell Signaling), MAPK antibody (Cell Signaling), β-actin mouse antibody (Santa Cruz Biotechnology).
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3

Evaluating EMT and Apoptosis Markers

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The cells of each group were collected and lysed, while the total protein was extracted. The protein concentration was examined by BCA, and we adjusted the protein concentration of each group. We loaded samples 30 μg/well, and electrophoresis was performed with SDS-PAGE gel. The protein was transferred to the PVDF membrane, sealed with skim milk at 25°C, incubated with primary antibody at 4°C overnight, incubated with HRP-linked secondary antibody, developed and photographed with an ECL kit. Primary antibodies included Snail antibody (ab216347), Twist antibody (ab50887), E-cadherin antibody (ab231303), N-cadherin antibody (ab76011), GSK3β antibody (ab32391), β-catenin antibody (ab32572), Bax antibody (ab32503), Bcl-2 antibody (ab182858), and GAPDH antibody (ab8245), all derived from Abcam.
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4

Western Blot Analysis of Cell Signaling Pathways

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The monoclonal human CAP1 antibody was previously described50 (link). Antibodies against GAPDH and GSK3 beta antibodies were from Santa Cruz Biotechnology Inc. (Santa Cruz, CA). E-cadherin antibody was from BD Biosciences (Franklin Lakes, NJ). Snail antibody was from Abcam (Cambridge, MA), and antibodies against ERK1/2, phosphor-ERK1/2 (Thr202/Tyr204), phosphor-cofilin, phospho-GSK3α/β (Ser21/Ser9), and FAK and phosphor-Y397 FAK were from Cell Signaling Technology Inc. (Danvers, MA). Cofilin antibody was from the Cytoskeleton Inc. (Denver, CO). Cell lysates were prepared for Western blotting similarly as previously described6 (link)51 (link).
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