Licensing
Description
Hela cells were treated with anti-SENP6 siRNA and synchronized by DTB for 48 hours. Cells were fixed and stained for kinetochore proteins Hec1 (green, Alexa Fluor 488 conjugated secondary Ab). Cells were simultaneously stained for centromeres (CREST, red, Alexa Fluor 568 conjugated secondary Ab) and Hoechst 33342 (blue). Fluorescence microscopy was performed at RT on a confocal microscope (LSM510 Meta; Carl Zeiss, Inc.) equipped with a 100× Plan-Apochromat objective. A543 nm HeNe laser (5 mW output; detection LP560 nm) was used for detection of Alexa Fluor 568–labeled antibodies. The 488nm line of an Argon laser (25 mW nominal output; detection BP 505–530 nm) was used for analysis of Alexa Fluor 488–labeled antibodies. Hoechst 33258 images were captured using the 364nm line of an ion laser (Enterprise II ML UV; Coherent, Inc.; 80 mW nominal output; detection BP 385–470 nm). Image Reference: PMID 20212317
Biological Sources
- NCBI Organism Classification
- Homo sapiens
- (human)
- Cell Line
- HeLa
- Cellular Component
- nuclear chromosome
- chromosome, centromeric region
Biological Context
- Biological Process
- cell cycle checkpoint
Attribution
- Names
- Debaditya Mukhopadhyay
- Alexei Arnaoutov
- Mary Dasso
- Published
- JCB 188:681–692, 2010
- Pubmed
- 20212317
Grouping
This image is part of a group.Imaging
- Image Type
- single-spot confocal microscopy
- Imaging Mode
- single-spot confocal microscopy
- Parameters Imaged
- fluorescence emission
- Source of Contrast
- differences in adsorption or binding of stain
- distribution of epitope
- Visualization Methods
- Hoechst 33342
- Alexa Fluor 488
- Alexa Fluor 568
Sample Preparation
- Methods
- formaldehyde fixed tissue
- Relation To Intact Cell
- whole mounted tissue
Dimensions
| Spatial Axis | Image Size | Pixel Size |
|---|---|---|
| X | 512px | —— |
| Y | 512px | —— |
| Z | 16 | —— |