<p>(A,E,I) DIC micrographs of three different dividing Chlamydomonas cells at the time of first cleavage furrow formation. (B,F,J) The immunofluorescence locations of α-tubulin (red), DAPI stained DNA (blue), and the indicated IFT protein (green) observed by widefield microscopy. (B,C) IFT27. (F,G) IFT72. (J,K) IFT46. (D,H,L) 3D reconstructions of optical sections obtained by laser scanning confocal microscopy of three additional dividing Chlamydomonas cells that were subjected to indirect immunofluorescence labeling at the time of cleavage furrow formation. Appearing in red is a reconstruction of each cell's microtubule cytoskeleton shown in side-view at the upper left and right of each panel. The locations of the cleavage furrows (cf) are...
(A) Fluorescence microscopy showing localization of CCP5A after fusion of the protein with GFP. CCP5...
<p>(A) Confocal micrographs showing localization of GFP, ZmGPDH4-GFP and ZmGPDH5-GFP. The merged pic...
<p>(A) Wide-field microscopy observation of the triple labelling of BILBO1, MORN1 and FPC4 on cytosk...
<p>(A). A representative TEM micrograph of a forming cleavage furrow (CF) is shown at a magnificatio...
<p>(A–I) Immunofluorescence microscopy. (A–C) Double stained fluorescence of acetylated tubulin and ...
(A) Combined transmitted and fluorescence image of dissected Drosophila cyst; dividing cells chosen ...
<div><p>Intraflagellar transport (IFT) proteins are well established as conserved mediators of flage...
In multi-nucleate cells of Dictyostelium, cytokinesis is performed by unilateral cleavage furrows th...
When using fluorescence microscope techniques to study cells, it is essential that the cell structur...
When using fluorescence microscope techniques to study cells, it is essential that the cell structur...
When using fluorescence microscope techniques to study cells, it is essential that the cell structur...
This image contains two fibroblast cells that were fixed on a microscope slide after being stained w...
After the separation of sister chromatids in anaphase, it is essential that the cell position a clea...
(A) Fluorescence maximum projection image capturing dividing cells from a dissected Drosophila cyst....
AbstractBackground: Myosin II, a conventional myosin, is dispensable for mitotic division in Dictyos...
(A) Fluorescence microscopy showing localization of CCP5A after fusion of the protein with GFP. CCP5...
<p>(A) Confocal micrographs showing localization of GFP, ZmGPDH4-GFP and ZmGPDH5-GFP. The merged pic...
<p>(A) Wide-field microscopy observation of the triple labelling of BILBO1, MORN1 and FPC4 on cytosk...
<p>(A). A representative TEM micrograph of a forming cleavage furrow (CF) is shown at a magnificatio...
<p>(A–I) Immunofluorescence microscopy. (A–C) Double stained fluorescence of acetylated tubulin and ...
(A) Combined transmitted and fluorescence image of dissected Drosophila cyst; dividing cells chosen ...
<div><p>Intraflagellar transport (IFT) proteins are well established as conserved mediators of flage...
In multi-nucleate cells of Dictyostelium, cytokinesis is performed by unilateral cleavage furrows th...
When using fluorescence microscope techniques to study cells, it is essential that the cell structur...
When using fluorescence microscope techniques to study cells, it is essential that the cell structur...
When using fluorescence microscope techniques to study cells, it is essential that the cell structur...
This image contains two fibroblast cells that were fixed on a microscope slide after being stained w...
After the separation of sister chromatids in anaphase, it is essential that the cell position a clea...
(A) Fluorescence maximum projection image capturing dividing cells from a dissected Drosophila cyst....
AbstractBackground: Myosin II, a conventional myosin, is dispensable for mitotic division in Dictyos...
(A) Fluorescence microscopy showing localization of CCP5A after fusion of the protein with GFP. CCP5...
<p>(A) Confocal micrographs showing localization of GFP, ZmGPDH4-GFP and ZmGPDH5-GFP. The merged pic...
<p>(A) Wide-field microscopy observation of the triple labelling of BILBO1, MORN1 and FPC4 on cytosk...