Fig. 3
- ID
- ZDB-FIG-091215-9
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- Tan et al., 2009 - Regulation of membrane progestin receptors in the zebrafish ovary by gonadotropin, activin, TGF-beta and BMP-15
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Regulation of mPRα and mRPβ by hCG (H), activin-A (A) and TGF-β1 (T). (A) Mid- to late growth phase follicles were treated with control medium (C), hCG (100 ng/ml), activin-A (100 ng/ml), TGF-β1 (10 ng/ml), for 12 and 18 h, and proteins were extracted from intact follicles and subjected to Western blotting. Equal loading was confirmed by Western blotting probed with an anti-α-tubulin antibody. (B) Histograms of normalized densitometry data for the 18 h time point (mean ± S.E.M.) from four experiments. Different letters denote statistical significance (p < 0.05). (C) Follicles were treated with hCG, activin-A, and TGF-β1 for 18 h and follicular cell layer was removed. Proteins were extracted from oocytes and Western blotting performed using mPRβ and α-tubulin antibodies. |
Reprinted from Molecular and Cellular Endocrinology, 312(1-2), Tan, Q., Zagrodny, A., Bernaudo, S., and Peng, C., Regulation of membrane progestin receptors in the zebrafish ovary by gonadotropin, activin, TGF-beta and BMP-15, 72-79, Copyright (2009) with permission from Elsevier. Full text @ Mol. Cell. Endocrinol.