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2 protocols using anti pepck

1

Immunoblotting Analysis of Liver and Muscle Proteins

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Immunoblotting was performed as described previously.17 (link) Isolated liver and skeletal muscle tissues were homogenized in lysis buffer. Cell lysates were heated at 100 °C for 5 min and subjected to electrophoresis on 8–15% (vol/vol) sodium dodecyl sulfate-polyacrylamide gels and transferred onto nitrocellulose membranes. Primary antibodies used were anti-LC3 (1:1000 dilution; Cell Signaling Technology Cat# 12741, RRID:AB_2617131), anti-p62 (1:1000 dilution; Cell Signaling Technology Cat# 5114, RRID:AB_10624872), anti-phospho-AMPKα (1; 1000 dilution; Cell Signaling Technology Cat# 2531, RRID:AB_330330), anti-AMPKα (1:1000 dilution; Cell Signaling Technology Cat# 2532, RRID:AB_330331), anti-phospho-p70 S6 kinase (1:1000 dilution; Cell Signaling Technology Cat# 9205, RRID:AB_330944), anti-p70 S6 kinase (1:1000 dilution; Cell Signaling Technology Cat# 9202, RRID:AB_331676), anti-GLUT4 (1:1000 dilution; Cell Signaling Technology Cat# 2213, RRID:AB_823508), anti-PEPCK (1:900 dilution; Abcam Cat# ab70358, RRID:AB_1925305), anti-G6Pase (1:500 dilution; Abcam Cat# ab133964) and β-actin (1:2000 dilution; Cell Signaling Technology Cat# 4967, RRID:AB_330288). The fluorescent bands were visualized using a detection system and quantified by densitometry (Amersham ECL Prime; GE Healthcare).
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2

ER Stress Pathway Modulators in Diabetes

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Avicularin (purity > 99%) and lead acetate were purchased from Sigma Chemical Co. (St. Louis, MO, USA). The anti-p-IRE1, anti-PERK, anti-p-eIF2α, anti-GRP78, anti-PYG, anti-GK, anti-PEPCK, anti-G6PC, anti-TNF-α, anti-IL-1β and anti-β-actin antibodies were provided by Abcam (Cambridge, MA, USA and Santa Cruz Biotechnology, CA, USA) [5 (link)].
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