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Maximum intensity projection of an optically cleared mouse brain labelled with Alexa 488-Neurofilame

Maximum intensity projection of an optically cleared mouse brain labelled with Alexa 488-Neurofilament (Cyan) and Alexa 568-Parvalbumin (Red). Original dataset was 800x800x1,000 micrometres.

Image courtesy of Adam Tyson, MRC Centre Developmental Neurobiology, King’s College London. (source)


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Multiphoton fluorescence image of HeLa cells with cytoskeletal microtubules (magenta) and DNA (cyan)

Multiphoton fluorescence image of HeLa cells with cytoskeletal microtubules (magenta) and DNA (cyan). Nikon RTS2000MP custom laser scanning microscope.

Source: National Center for Microscopy and Imaging Research (NCMIR) (source)

Credit Line: National Center for Microscopy and Imaging Research


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 #Lipilight #MemBright and super resolution #LiveSR on living muscle cells! by Bruno CadotVisit webs #Lipilight #MemBright and super resolution #LiveSR on living muscle cells! by Bruno CadotVisit webs #Lipilight #MemBright and super resolution #LiveSR on living muscle cells! by Bruno CadotVisit webs

#Lipilight#MemBright and super resolution #LiveSR on living muscle cells! by Bruno Cadot

Visit website : https://cadotbruno.com

Visit Bruno’s Twitter : https://twitter.com/cadotbru


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Top: Drawings of mitosis in newt cells found in W. Flemming, Zellsubstanz, kern und zelltheilung (VeTop: Drawings of mitosis in newt cells found in W. Flemming, Zellsubstanz, kern und zelltheilung (Ve

Top: Drawings of mitosis in newt cells found in W. Flemming, Zellsubstanz, kern und zelltheilung (Verlag Vogel, Leipzig, 1882). (A to J) During prophase (A to C) the chromosomes form within the nucleus from a substance termed “chromatin” because of its affinity for dyes. After nuclear envelope breakdown (D), the chromosomes interact with the two separating “centrosomes” (E) to form a spindle-shaped structure (E and F). After the chromosomes attach to the spindle, they become positioned on its equator, halfway between the two poles (G). Once this “metaphase” stage is achieved, the two chromatids comprising each chromosome disjoin and move toward the opposing poles (G and H). During the final stages of mitosis, neighboring chromosomes within the two groups fuse to form the daughter nuclei (H and I), and the cell becomes constricted between them (I) by cytokinesis. (J) Drawing from Schrader’s (2) book depicting conspicuous chromosomal (kinetochore) fibers during early anaphase inLilium.

Bottom: (A to H) Fluorescence micrographs of mitosis in fixed newt lung cells stained with antibodies to reveal the microtubules (green), and with a dye (Hoechst 33342) to reveal the chromosomes (blue). The spindle forms as the separating astral MT arrays, associated with each centrosome (A to C), interact with the chromosomes. Once the chromosomes are segregated into daughter nuclei (F and G), new MT-based structures known as stem-bodies form between the new nuclei (G). These play a role in cytokinesis (H).

Source : Rieder C.L. & Khodjakov A.; Mitosis Through the Microscope: Advances in Seeing Inside Live Dividing Cells; Science  04 Apr 2003:Vol. 300, Issue 5616, pp. 91-96 DOI: 10.1126/science.1082177


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