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. 2012 Jul 1;5(4):345–349. doi: 10.4161/cib.20348

graphic file with name cib-5-345-g2.jpg

Figure 2. Nuclear envelope of a Xenopus laevis oocyte as seen by dSTORM.33 (A) Nuclear envelopes isolated from Xenopus laevis oocytes were labeled with Alexa647 by indirect immunofluorescence against gp210, a protein that localizes to the lumen of the nuclear envelope bordering the pore wall. (B) Higher magnifications reveal the structural arrangement of gp210 proteins in nuclear pore complexes (NPCs). The 8-fold symmetry of the gp210 ring around each NPC (B) and the diameter of the central channel of ~40 nm is correctly identified with an optical resolution of ~15 nm (C) using WGA-Alexa647 binding to nucleoporins of the central channel (ref. 33). Scale bars: 500 nm (A), 150 nm (B, C).