2010
DOI: 10.1016/s0091-679x(10)96017-2
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Electron Microscopy of the Amphibian Model Systems Xenopus laevis and Ambystoma mexicanum

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Cited by 27 publications
(23 citation statements)
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“…For semi-thin sections and electron microscopy, zebrafish hearts were fixed in modified Karnovsky's fixative (2% glutaraldehyde +2% paraformaldehyde in 50 mM HEPES, [27], [28]) at 4°C overnight, and washed 2x in 100 mM HEPES and 2x in PBS. For light microscopy the samples were embedded in the methacrylate Technovit 7100 (Heraeus-Kulzer).…”
Section: Methodsmentioning
confidence: 99%
“…For semi-thin sections and electron microscopy, zebrafish hearts were fixed in modified Karnovsky's fixative (2% glutaraldehyde +2% paraformaldehyde in 50 mM HEPES, [27], [28]) at 4°C overnight, and washed 2x in 100 mM HEPES and 2x in PBS. For light microscopy the samples were embedded in the methacrylate Technovit 7100 (Heraeus-Kulzer).…”
Section: Methodsmentioning
confidence: 99%
“…Immunogold labeling was performed as described (Kurth et al, 2010; see Appendix and Table 1), and samples analyzed on a Morgagni D268 (FEI) or a JEM1400 Plus (JEOL) at 80 kV acceleration voltage.…”
Section: Electron Microscopymentioning
confidence: 99%
“…Actin dynamics were viewed in LifeAct mRNA-injected cells using a Carl Zeiss LSM 510 confocal microscope. For transmission electron microscopy, gastrula explants were fixed in 2.5% glutaraldehyde/2% formaldehyde, post-fixed with 1% osmium tetraoxide and infiltrated with Spurr's resin as described (Kurth et al, 2010). Ultrathin sections were stained with uranyl acetate and post-stained with Reynold's lead citrate.…”
Section: Microscopymentioning
confidence: 99%