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5 protocols using gadph

1

Western Blot Analysis of EMT Markers

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The expression levels of GOLM1, E-cadherin, Vimentin, TGF-β1, Smad2, p-Smad2, and
GADPH were detected by Western blotting. First, equal amounts of proteins were
loaded onto 10% SDS-PAGE gels for separation and then transferred to
polyvinylidene fluoride membrane (Bio-Rad). Second, the membranes were blocked
with 5% nonfat milk for 2 h and then were incubated with primary antibodies, and
placed on shaker, at 4 °C overnight. Indicated primary antibodies in this study
were polyclonal rabbit antibodies against GOLM1 (1:1000 dilution; Affinity),
E-cadherin (1:5000 dilution; Proteintech), Vimentin (1:1000 dilution;
Proteintech), TGF-β1 (1:1000 dilution; Abclonal), Smad2 (1:1000 diluton;
Affinity), p-Smad2 (1:1000) and GADPH (1:1000 dilution; Affinity). Third, the
membranes were incubated with HRP-conjugated anti-rabbit secondary antibodies
(1:600 dilution; Beyotime Biotechnology) after washing with TBST buffer.
Finally, the protein levels were detected by using an enhanced chemiluminescence
system (ECL Kit, Pierce Biotechnology) and captured on light-sensitive Xrayfilm
(Carestream). The optical densities of bands were analyzed by ImageJ
software.
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2

Western Blot Analysis of Stem Cell Markers

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Cells were lysed in RIPA (CWBio, Beijing, China) containing protease inhibitors, on ice. The lysates were mixed with loading buffer and denatured at 100 °C for 10 min. The products were then subjected to sodium dodecylsulfate-polyacrilamide gel electrophoresis (SDS-PAGE) and transferred to polyvinylidene difluoride (PVDF) membranes (Millipore, Billerica, Massachusetts, USA). The membranes were incubated with primary antibodies [SOX2 (CST, 1:1000), SOX9 (Abcam, 1:5000), CD133 (Proteintech, 1:1000), Nestin (Proteintech, 1:1000), PTN (Abcam, 1:1500) and GADPH (Affinity, 1:1000)] and then the secondary antibody, which was conjugated to horseradish peroxidase (HRP;anti-rabbit IgG/anti-mouse IgG, CST, 1:5000). Immunoreative bands were visualized using Image Lab after the addition of luminol-based chemiluminescent substrate (ECL; Millipore). The immunobloting results were analyzed using Image Lab software.
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3

Western Blot Analysis of Protein Interactions

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Cells were lysed in RIPA (CWBio, Beijing, China) containing protease inhibitors, on ice. The lysates were mixed with loading buffer and denatured at 100 °C for 10 min. The products were then subjected to sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) and transferred to polyvinylidene difluoride (PVDF) membranes (Millipore, Billerica, Massachusetts, USA). The membranes were incubated with primary antibodies [TRIM22 (Abcam, ab224059), KAT2A (CST, ab217876), FLAG (Abcam, ab205606), Myc (Abcam, ab32072), Ub (Abcam, ab140601) and GADPH (Affinity, 1:1000)] and then the secondary antibody, which was conjugated to horseradish peroxidase (HRP;anti-rabbit IgG/anti-mouse IgG, CST, 1:5000). Immunoreactive bands were visualized using Image Lab after the addition of luminol-based chemiluminescent substrate (ECL; Millipore). The immunoblotting results were analyzed using Image Lab software.
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4

Biochemical Assays for Cellular Stress

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Assay kits for detecting BUN, CREA, tumor necrosis factor-α (TNF-α), interleukin (IL)-8, reactive oxygen species (ROS) and superoxide dismutase (SOD) were purchased form Nanjing Jiancheng Bioengineering Institute (Nanjing, China).
Antibodies LC3, Beclin 1, AMPK, phosphorylated-AMPK (p-AMPK, Thr172), mTOR, phosphorylated-mTOR (p-mTOR, Ser2448), cleaved caspase 3, pro-caspase-3, Bcl-2, Bax and glyceraldehyde-3-phosphate dehydrogenase (GADPH) were ordered from Affinity (Changzhou, China). DB was obtained from ChemFaces (Wuhan, China). Compound C (CC), the specific AMPK signaling blocker, was purchased from MedChemExpress (Shanghai, China).
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5

Ovarian Tissue Protein Analysis

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The total protein of ovarian tissues and GCs was extracted by radioimmunoprecipitation buffer (P0013D, Biyuntian), separated with 10% SDS-PAGE and transferred to PVDF membranes. After hindering with 5% nonfat milk, the membranes were incubated overnight at 4 °C with primary antibodies against Bcl-2 (AF6139), Bax (AF0120), Bad (AF6471), IGF-1 (DF6096), PI3K (AF7022), p-PI3K (AF3242), AKT (AF4718), p-AKT (AF0016), and GAPDH (AF7021). Then, the membranes were probed with HRP-conjugated secondary antibody (1:600, DF6096, CST) for 1 h. The bands were visualized using chemiluminescence and quantified by ImageJ software. GAPDH served as an internal control. All primary antibodies were purchased from Affinity and used at a dilution of 1:1000, except for GADPH, which was used at a dilution of 1:10,000.
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