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4 protocols using anti p perk thr980

1

Protein Expression Analysis Protocol

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All protein samples were quantified by using the BCA reagent (Beyotime). Anti‐CSE, anti‐DGAT1, anti‐SREBP1, anti‐AGPAT3, anti‐CHOP, anti‐eIF2α, anti‐PERK, anti‐BIP, anti‐β‐Tubulin, anti‐SYVN1 and anti‐Ubiquitin were from Proteintech. Anti‐P‐eIF2α (Ser51) and anti‐P‐PERK (Thr980) were from Cell Signalling Technology. Specific bands were recorded via a chemiluminescence detection system (Thermo). The band intensity was conducted by ImageJ tool.
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2

Biochemical Profiling of Autophagy Pathways

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RL71 (>97% purity, HPLC) was synthesized as described previously.14 (link) anti-LC3B, anti-ubiqutin, anti-CHOP, anti-PARP, anti-p-JNK, anti-JNK, anti-p-PERK (Thr980), anti-p-AMPK (Thr172), anti-p-mTOR (Ser2448, 2971), anti-p-p70S6K (Thr389), anti-Cox4 and anti-cleaved caspase-3 antibodies were purchased from Cell Signaling Technology (Beverly, MA, USA). Anti-Grp78, anti-ATF4, anti-ATF6, anti-β-actin and anti-GFP antibodies were from Santa Cruz Biotechnology (Santa Cruz, CA, USA). Anti-SQSTM1/p62, anti-ATG5 and anti-ATG7 antibodies were from Abcam (Cambridge, UK) and anti-LC3 was from Novus Biologicals (Littleton, CO, USA). GFP-LC3 plasmid was purchased from Yingrun Biotechnologies Inc. (Changsha, China). Compound C (CC) and BAPTA were obtained from Calbiochem (San Diego, CA, USA). zVAD was from Selleck Chemicals (Houston, TX, USA). Chloroquine (CQ), STO-609, SP600125 and PBA were purchased from Sigma-Aldrich (St. Louis, MO, USA). The ER-specific dye ER tracker Red, the mitochondrial specific dye MitoTraker Red CMXRos (M7512), JC-1 (T-3168), Fura-2/AM and Lipofectamine 3000 transfection reagent were purchased from Life Technologies (Grand Island, NY, USA). The Ca2+-ATPase activity assay kit was purchased from Nanjing Jiancheng Bioengineering Institute (Nanjing). All of the other chemicals were purchased from Sigma-Aldrich.
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Western Blot Analysis of Protein Targets

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Western blotting was performed as described previously. Primary antibodies included anti-CSE (Proteintech, Rosemont, IL, USA), anti-SERCA2a (Invitrogen, Carlsbad, CA, USA), anti-Ubiquitin (Proteintech), anti-eIF2α (Proteintech), anti-P-eIF2α (Ser51, Cell Signaling Technology, Danvers, MA, USA), anti-PERK (Proteintech), anti-P-PERK (Thr-980, Cell Signaling Technology), anti-Bip (Proteintech), anti-CHOP (Proteintech), anti-MuRF1 (Proteintech), anti-Caspase3 (Proteintech), anti-β-Tubulin (Proteintech). The primary antibody was incubated overnight at 4 °C. Density measurements were performed using the image processing and analysis program alphaview SA (3.3.0, provided by ProteinSimple), and data were expressed in relative units.
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4

Western Blot Analysis of Protein Targets

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Western blotting was performed as described previously. Primary antibodies included anti‐CSE (Proteintech,1:1000), anti‐CHOP (Proteintech, 1:1000), anti‐Ubiquitin (Proteintech, 1:1000), anti‐eIF2α (Proteintech, 1:1000), anti‐P‐eIF2α (Ser51, Cell Signaling Technology, 1:1000), anti‐DGAT1 (Proteintech, 1:1000), anti‐DGAT2(Signalway Antibody, 1:1000), anti‐PERK (Proteintech, 1:1000), anti‐P‐PERK (Thr‐980, Cell Signaling Technology, 1:1000), anti‐Bip (Proteintech, 1:1000), anti‐Hrd1 (Proteintech, 1:1000), anti‐perilipin2 (Proteintech, 1:1000), anti‐collagen I (Proteintech, 1:1000), anti‐collagen Ⅲ (Proteintech, 1:1000), anti‐GAPDH (Proteintech, 1:1000). Primary antibodies were incubated overnight at 4℃. Densitometry was conducted with image processing and analysis program AlphaView.SA and the data were expressed as relative units.
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