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CDC20 appears to act as a regulatory protein interacting with several other proteins at multiple points in the cell cycle. Zusätzlich bieten wir Ihnen CDC20 Proteine (7) und CDC20 Kits (2) und viele weitere Produktgruppen zu diesem Protein an.
Showing 10 out of 266 products:
Human Polyclonal CDC20 Primary Antibody für ICC, IF - ABIN252981
Di Fiore, Pines: How cyclin A destruction escapes the spindle assembly checkpoint. in The Journal of cell biology 2010
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Human Polyclonal CDC20 Primary Antibody für ICC, IF - ABIN252980
Ahlskog, Björk, Elsing, Aspelin, Kallio, Roos-Mattjus, Sistonen: Anaphase-promoting complex/cyclosome participates in the acute response to protein-damaging stress. in Molecular and cellular biology 2010
Show all 2 Pubmed References
Xenopus laevis Monoclonal CDC20 Primary Antibody für CyTOF, ELISA - ABIN251088
Sackton, Dimova, Zeng, Tian, Zhang, Sackton, Meaders, Pfaff, Sigoillot, Yu, Luo, King: Synergistic blockade of mitotic exit by two chemical inhibitors of the APC/C. in Nature 2014
Human Polyclonal CDC20 Primary Antibody für IP, WB - ABIN233786
Yamamuro, Kano, Naito: Functions of FZR1 and CDC20, activators of the anaphase-promoting complex, during meiotic maturation of swine oocytes. in Biology of reproduction 2008
Human Polyclonal CDC20 Primary Antibody für IHC, IHC (p) - ABIN4296835
Onul, Colvard, Paradise, Elseth, Vesper, Gouvas, Deliu, Garcia, Pestle, Radosevich: Application of immunohistochemical staining to detect antigen destruction as a measure of tissue damage. in The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society 2012
Long non-coding RNA SPRY4 (zeige SPRY4 Antikörper)-IT1 (zeige HAUS3 Antikörper) promotes cell proliferation and invasion by regulation of Cdc20 in pancreatic cancer cells
Cdc20 functions as an important negative regulator of SMAR1 (zeige BANP Antikörper) in higher grades of cancer
Data provide support for the recent structure-based models and functionally dissect three elements of Cdc20 inhibition: sequestration of Cdc20 in the core mitotic checkpoint (zeige BUB3 Antikörper) complex, sufficient at low Cdc20 concentrations; inhibition of a second Cdc20 through the Mad3 (zeige SMAD3 Antikörper) C terminus, independent of Mad2 (zeige MAD2L1 Antikörper) binding to this Cdc20 molecule; and occupancy of the APC (zeige APC Antikörper)/C with full MCC (zeige MCC Antikörper), where Mad3 (zeige SMAD3 Antikörper) and Apc15 (zeige ANAPC15 Antikörper) are involved.
CDC20 gene, related to cell proliferation in protein complex A, might play momentous roles in the initiation and development of consecutive Trauma-Induced Sepsis.
A mitotic phosphorylation site on Cdc20, known to be a substrate of PP2A (zeige PPP2R4 Antikörper)(B56), modulates APC (zeige APC Antikörper)/C(Cdc20) assembly.
c-Myc (zeige MYC Antikörper) is a driver when combined with kRas/Akt3 (zeige AKT3 Antikörper) oncogenic signals in gliomagenesis, whereas Cdc20 overexpression is a passenger
The ABBA (zeige MTSS1L Antikörper)-KEN (zeige PCNT Antikörper)-ABBA (zeige MTSS1L Antikörper) amino acid motif cassette holds the Mitotic Checkpoint (zeige BUB3 Antikörper) Complex (MCC (zeige MCC Antikörper)) onto the Anaphase-Promoting Complex-Cyclosome (APC (zeige APC Antikörper)/C) by binding the two Cdc20 molecules in the MCC (zeige MCC Antikörper)-APC (zeige APC Antikörper)/C complex.
It discuses the roles of Cdc20 in SAC (zeige ADCY10 Antikörper) signalling and mitotic exit, describe how the integration of traditional approaches with emerging technologies has revealed new details of Cdc20 functions, comment about the potential of Cdc20 as a therapeutic target for the treatment of human malignancies.
Prostate cancer-derived SPOP (zeige SPOP Antikörper) mutants failed to interact with Cdc20 to promote its degradation. As a result, SPOP (zeige SPOP Antikörper)-deficient prostate cancer cells with elevated Cdc20 expression became resistant to a pharmacological Cdc20 inhibitor.
High CDC20 expression is associated with metastatic castration-resistant prostate cancer growth and reduces chemosensitivity .
Cdc20 auto-ubiquitylation does not play a major role in terminating Cdc20 activation.
Dephosphorylation of Cdc20 is required for its loading and activation of the APC/C ubiquitin ligase.
A role for the fizzy/cdc20 family of proteins in activation of the APC (zeige APC Antikörper)/C distinct from substrate recruitment is reported.
Cdc20 hypomorphism causes chromatin bridging and chromosome misalignment, revealing a requirement for Cdc20 in efficient sister chromosome separation and chromosome-microtubule attachment.
The physiologically effective threshold level of Cdc20 is high for female meiosis I.
Results indicate that Cdc20 also contributes to post-anaphase activation of the APC (zeige APC Antikörper)/C.
The seven tandem WD motifs of Cdc20 they are required for speriolin binding and for localization of Cdc20 to the centrosomes and nucleus, suggesting that speriolin might regulate or stabilize the folding of Cdc20 during meiosis in spermatogenic cells
Data suggest that Mad2 (zeige MXI1 Antikörper) and BubR1 (zeige BUB1B Antikörper) must cooperate to inhibit Cdc20 activity.
Cdc20 is degraded through two independent degradation signals (degrons), the KEN (zeige PCNT Antikörper) box and a newly described CRY (zeige CRY2 Antikörper) box.
Cdc20 and securin (zeige PTTG1 Antikörper) double mutant embryos could not maintain the metaphase arrest, suggesting a role of securin (zeige PTTG1 Antikörper) in preventing mitotic exit
Expression of the cdc20 gene is down-regulated by zif268 (zeige EGR1 Antikörper) in neuronal cells; altered expression of proteasome-regulatory genes following zif268 (zeige EGR1 Antikörper) induction may be a key component of long-lasting CNS plasticity.
Cdc20 is required for the anaphase onset of the first meiosis but not the second meiosis in mouse oocytes
findings suggest a novel function of HSF1 (zeige HSF1 Antikörper) frequently overexpressed in cancer cells, to inhibit APC (zeige APC Antikörper)/C activity by interacting with Cdc20, and to result in aneuploidy development and genomic instability
porcine FZR1 (zeige FZR1 Antikörper) and CDC20 work on the maintenance of meiotic arrest at the first meiotic prophase and on the exit from M1
CDC20 appears to act as a regulatory protein interacting with several other proteins at multiple points in the cell cycle. It is required for two microtubule-dependent processes, nuclear movement prior to anaphase and chromosome separation.
cell division cycle 20 homolog
, CDC20 cell division cycle 20 homolog
, cell division cycle protein 20 homolog
, cell cycle protein p55CDC