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2 protocols using anti loxl2

1

Western Blot Analysis of LOXL2 Protein

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Protein extracts were generated as previously described (18 (link)). Samples were separated on NuPAGE 4–12% Bis-Tris gels (Invitrogen) and then transferred to Immobilon P membranes (Millipore, Temecula, CA). Proteins were detected using rabbit anti-LOXL2 (Abcam, Cambridge, MA) and β-actin antibodies (Santa Cruz Biotechnology) listed in Supplementary Table 2 and enhanced chemiluminescence detection reagents (Amersham, Piscataway, NJ).
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2

Fibrosis Signaling Pathway Modulation

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BLM and the JNK inhibitor (SP600125) were obtained from Selleck China Inc. (Shanghai, China). TGF-β1 was purchased from PeproTech China Inc. (Suzhou, China). Azithromycin was obtained from Sigma-Aldrich Inc. (Shanghai, China). The primary antibodies we used are as follows: anti-vimentin (Proteintech, 60330-1-Ig), anti-alpha-smooth muscle actin (α-SMA) (Proteintech, 14395-1-AP), anti-Collagen 1 (Proteintech, 14695-1-AP), anti-LOX (Proteintech, 17958-1-AP), anti-LOXL2 (Abcam, 96233), anti-TGF-β1 (Proteintech, 21898-1-AP), anti-Smad2 (Cell Signaling Technology, 5339), anti-Smad3 (Cell Signaling Technology, 9523), anti-phospho (P)-smad2 (Cell Signaling Technology, 3108), anti-P-smad3 (Cell Signaling Technology, 9520), anti-JNK (Proteintech, 66210-1-Ig), anti-c-Jun (Proteintech, 66313-1-Ig), anti-P-JNK (Proteintech, 80024-1-RR), anti-P-cJun (Proteintech, 28891-1-AP), anti-α-tubulin (Proteintech, 66031-1-Ig), and anti-GAPDH (Proteintech, 60004-1-Ig). The dilution ratio of all antibodies was 1:1000.
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