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4 protocols using ab80633

1

Protein Extraction and Fractionation Protocol

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Cell Lysis Buffer (CST) was used to extract protein lysates and the Subcellular Protein Fractionation Kit for Cultured Cells (ThermoFisher Scientific) was used for fractionation according to manufacturers’ instructions. The following primary antibodies were used: EZH2 (5246; CST), GAPDH (MAB374; Merck Millipore), Histone H3 (ab1791; Abcam), H3K27me3 (ab6002; Abcam), MYOG (556,358; BD Biosciences), p16 (ab108349; Abcam), p21 (ab80633; Abcam), PARP (9542; CST), RARα (E6Z6K; CST), α-Skeletal Muscle Actin (ab28052; Abcam), α-Tubulin (SC-8035; Santa Cruz Technology). Immunostained bands were detected by chemiluminescence (GE Healthcare). Full length blots in Additional File 1.
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Western Blot Analysis of Cell Signaling

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Transfected cells were collected and lysed in lysate buffer (Beyotime, Beijing, China). Protein concentration was determined using bicinchoninic acid (BCA) protein assay kit (Pierce, Rockford, IL, USA), and protein samples were separated on sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) and then transferred to nitrocellulose membrane (Whatman, Dassel, Germany). After blocking with 5% nonfat milk for 2 h, the membranes were incubated with the primary antibodies overnight, and horseradish peroxidase-conjugated secondary antibody was used for 2 h. Finally, protein bands were visualized using the enhanced chemiluminescence (ECL) reagent (GE Healthcare, Little Chalfont, UK), and optical density was calculated by ImageJ software version 1.49 (National Institutes of Health, Bethesda, MD, USA).
Antibodies used were as follows: actin (C-2) was purchased from Santa Cruz Biotechnology (Santa Cruz, CA, USA). p27 (ab54563), p21 (ab80633), Bcl-2 (ab692), Bax (ac32503), cleaved caspase 3 (ab32042), procaspase 3 (ab2171), and horseradish peroxidase-conjugated anti-mouse (ab6785) and anti-rabbit antibodies (ab6721) were purchased from Abcam (Cambridge, MA, USA).
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3

Immunohistochemical Analysis of Ovarian Tissues

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Paraffin-embedded ovary tissue was sectioned at 4 μm thickness, deparaffinized in xylene, and rehydrated in a graded series of alcohols. After antigen retrieval, 3% hydrogen peroxide was used to block endogenous peroxidase. The sections were incubated in serum for blocking and subsequently incubated with primary antibodies against proliferating cell nuclear antigen (PCNA, 13110, CST), p-JNK (4668, CST), p-p38 MAPK (4511, CST), p21 (ab80633, Abcam), p22phox (sc-271968, Santa Cruz Biotechnology), and p47phox (sc-17844, Santa Cruz Biotechnology) overnight at 4°C before being incubated with a secondary antibody and treated with a diaminobenzidine (DAB) staining kit (Zhongshanjinqiao, Beijing, China). The slides were examined with an Olympus BX63 microscope.
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4

Immunohistochemistry and BrdU Analysis

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Tissues were separated after the sacrifice of rats, and fixed with 10% formalin for 24 h. OCT compound was used for tissue embedding, and 10-μm thickness tissues were achieved using a frozen microtome. Mouse anti-P21 antibody (ab80633, Abcam, Cambridge, UK) and mouse anti-PCNA antibody (ab29, Abcam, Cambridge, UK) were used in this study. Then, incubation with biotinylated secondary antibody and visualization with Vectastain Elite ABC HRP kit. Zeiss AxioVision was applied for visualizing.
For the BrdU staining, the BrdU was firstly dissolved into 10 mg/mL using PBS. The animals were treated with BrdU (100 mg/kg) through intraperitoneal injection. Tissue separation, embedding, section, and fixation were conducted as described above. Then, the sections were incubated with a mouse monoclonal anti-BrdU antibody (Abcam, Cambridge, UK). The proliferation data of tissues were analyzed by counting the BrdU stained positive cells (nuclei).
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