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3D structured illumination microscopy of mammalian embryos and spermatozoa
BACKGROUND: Super-resolution fluorescence microscopy performed via 3D structured illumination microscopy (3D-SIM) is well established on flat, adherent cells. However, blastomeres of mammalian embryos are non-adherent, round and large. Scanning whole mount mammalian embryos with 3D-SIM is prone to f...
Autores principales: | Popken, Jens, Dahlhoff, Maik, Guengoer, Tuna, Wolf, Eckhard, Zakhartchenko, Valeri |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4661982/ https://www.ncbi.nlm.nih.gov/pubmed/26610350 http://dx.doi.org/10.1186/s12861-015-0092-7 |
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