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. 2015 Nov 14;13:124. doi: 10.1186/s12958-015-0122-0

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© Dadarwal et al. 2015

Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

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Fig. 2 — Electron micrographs (photographed at a primary magnification of 3000x) representing peripheral (Pp, a), perinuclear (Pn, b), and central (c) regions of ooplasm as well as the central region overlayed with the transparent grid for stereology (c). d, e, f, g, h illustrate cortical granules (CG), Golgi complex (G), hooded (HM) and non-hooded mitochondria (N-HM), vesicles (V), smooth endoplasmic reticulum (SER), and lipid droplets (LD) identified in the ooplasm for the quantitative data. Note the close spatial association between hooded-mitochondria (HM) and SER (e); and non-hooded mitochondria (N-HM) and lipid droplet (h). d, e, f and g represents peripheral ooplasm and (h) represent perinuclear ooplasm of an oocyte from D6W1 follicle, respectively. ZP = zona pellucida. Nu = nucleus