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...

Descripción completa

Detalles Bibliográficos
Autores principales: Popken, Jens, Dahlhoff, Maik, Guengoer, Tuna, Wolf, Eckhard, Zakhartchenko, Valeri
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Methodology Article
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

Internet

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

Ejemplares similares