Licensing
Description
Z-focal series through HeLa cell in mitosis illustrating MCAK localization in Bod1siRNA cells. Cells were transfected with control (CIL: 13377) or Bod1 (this image) siRNA. After 72 h, cells were treated with monastrol for 3 h and released into media containing MG132 for 1 h before fixing. Cells were stained for total mitotic centromere-associated kinesin (MCAK) population. MCAK localizes to the inner centromere in its phosphorylated form but concentrates at kinetochores in its dephosphorylated state.
Technical Details
Antibodies were rabbit anti-HEC1 (green) antibody (Abcam) used at 1:1,000. and sheep anti-MCAK (red) (Andrews et al., 2004) used at 1 μg/ml, and DNA (blue). Fluorescently labeled secondary antibodies were all obtained from Jackson ImmunoResearch Laboratories. Corresponds to Fig 5B in JCB vol. 179 no. 2 187-197.
Biological Sources
- NCBI Organism Classification
- Homo sapiens
- (human)
- Cell Line
- HeLa S3
- Cellular Component
- chromosome, centromeric region
- DNA
- HEC1
- MCAK
Biological Context
- Biological Process
- mitosis
- Bod1 siRNA
Attribution
- Names
- Iain M. Porter
- Sarah E. McClelland
- Guennadi A. Khoudoli
- Christopher J. Hunter
- Jens S. Andersen
- Andrew D. McAinsh
- J. Julian Blow
- Jason R. Swedlow
- Published
- JCB vol. 179 no. 2 187-197
- Link
- Journal of Cell Biology
- Pubmed
- 17938248
Grouping
This image is part of a group.Imaging
- Image Type
- recorded image
- Imaging Mode
- fluorescence microscopy
- Parameters Imaged
- fluorescence emission
- Source of Contrast
- distribution of a specific protein
- Visualization Methods
- primary antibody plus labeled secondary antibody
- Processing History
- constrained iterative deconvolution
Sample Preparation
- Methods
- chemically fixed tissue
- Relation To Intact Cell
- dispersed cells in vitro
Dimensions
| Spatial Axis | Image Size | Pixel Size |
|---|---|---|
| X | 377px | 0.0629μm |
| Y | 389px | 0.0629μm |
| Z | 42 | .2μm |