mProX™ Human CDC20 Stable Cell Line
- Product Category:
- Membrane Protein Stable Cell Lines
- Subcategory:
- Kinase Cell Lines
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Published Data
Fig.1 Cdc20 phosphorylation prevents interphase APC/C binding.
After removing endogenous Cdc20 from stable HeLa cell lines expressing the corresponding YFP-tagged Cdc20 proteins, YFP-Cdc20 complexes were purified eight hours after the cells were released from a thymidine block. SDS-PAGE was used to analyze the samples, and LI-COR technology was used to quantify the results of probing for APC1, APC3, and APC7.
Ref: Hein, Jamin B., and Jakob Nilsson. "Interphase APC/C-Cdc20 inhibition by cyclin A2-Cdk2 ensures efficient mitotic entry." Nature communications 7.1 (2016): 10975.
Pubmed: 26960431
DOI: 10.1038/ncomms10975
Research Highlights
The Anaphase Promoting Complex (APC, also known as APC/C) forms two functionally independent but functionally linked E3 ubiquitin ligase sub-complexes, APC(Cdc20) and APC(Cdh1), respectively, that govern the advancement of the cell cycle.
Wang, Lixia, et al. "Targeting Cdc20 as a novel cancer therapeutic strategy." Pharmacology & therapeutics 151 (2015): 141-151.
Pubmed:
25850036
DOI:
10.1016/j.pharmthera.2015.04.002
Important roles for cell-division cycle protein 20 homologue (Cdc20) include chromosomal segregation and mitotic exit. Targeted by the spindle assembly checkpoint (SAC), Cdc20 is also an essential cofactor of the anaphase-promoting complex or cyclosome (APC/C) E3 ubiquitin ligase, which controls APC/C ubiquitin activity on particular substrates in preparation for the proteasome's eventual destruction.
Kapanidou, Maria, Natalie L. Curtis, and Victor M. Bolanos-Garcia. "Cdc20: at the crossroads between chromosome segregation and mitotic exit." Trends in biochemical sciences 42.3 (2017): 193-205.
Pubmed:
28202332
DOI:
10.1016/j.tibs.2016.12.001