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CDC20 appears to act as a regulatory protein interacting with several other proteins at multiple points in the cell cycle. 再加上，我们可以发CDC20 蛋白 (7) 和 CDC20 试剂盒 (1)和数多这个蛋白质的别的产品。
Showing 10 out of 217 products:
Human Polyclonal CDC20 Primary Antibody for 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 for 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
Human Polyclonal CDC20 Primary Antibody for 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
Xenopus laevis Monoclonal CDC20 Primary Antibody for 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 for 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
c-Myc (显示 MYC 抗体) is a driver when combined with kRas/Akt3 (显示 AKT3 抗体) oncogenic signals in gliomagenesis, whereas Cdc20 overexpression is a passenger
The ABBA (显示 MTSS1L 抗体)-KEN (显示 PCNT 抗体)-ABBA (显示 MTSS1L 抗体) amino acid motif cassette holds the Mitotic Checkpoint (显示 BUB3 抗体) Complex (MCC (显示 MCC 抗体)) onto the Anaphase-Promoting Complex-Cyclosome (APC (显示 APC 抗体)/C) by binding the two Cdc20 molecules in the MCC (显示 MCC 抗体)-APC (显示 APC 抗体)/C complex.
It discuses the roles of Cdc20 in SAC (显示 ADCY10 抗体) 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 (显示 SPOP 抗体) mutants failed to interact with Cdc20 to promote its degradation. As a result, SPOP (显示 SPOP 抗体)-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 .
These results provide novel insight into the mechanisms underlying the aberrant capability of NUP98 (显示 NUP98 抗体) oncoproteins to interact with APC (显示 APC 抗体)/C(Cdc20) and to interfere with its function.
In lung adenocarcinoma patients, overexpression of cell division cycle 20 was significantly associated with bigger primary tumor size, higher MKI67 (显示 MKI67 抗体) level, higher DNA ploidy level, and poor prognosis.
CDC20 may have a role in carcinoma of the breast, colon, endometrium, and prostate
Overexpression of Cdc20 may serve as an independent predictor for biochemical recurrence in patients of clinically localized prostate cancer undergoing laparoscopic radical prostatectomy without neoadjuvant therapy.
Results show that CYP1B1 (显示 CYP1B1 抗体) may promote renal cell carcinoma (显示 MOK 抗体) development by inducing CDC20 expression and inhibiting apoptosis through the down-regulation of DAPK1 (显示 DAPK1 抗体).
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 (显示 APC 抗体)/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 (显示 APC 抗体)/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 (显示 MXI1 抗体) and BubR1 (显示 BUB1B 抗体) must cooperate to inhibit Cdc20 activity.
Cdc20 is degraded through two independent degradation signals (degrons), the KEN (显示 PCNT 抗体) box and a newly described CRY (显示 CRY2 抗体) box.
Cdc20 and securin (显示 PTTG1 抗体) double mutant embryos could not maintain the metaphase arrest, suggesting a role of securin (显示 PTTG1 抗体) in preventing mitotic exit
Expression of the cdc20 gene is down-regulated by zif268 (显示 EGR1 抗体) in neuronal cells; altered expression of proteasome-regulatory genes following zif268 (显示 EGR1 抗体) 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 (显示 HSF1 抗体) frequently overexpressed in cancer cells, to inhibit APC (显示 APC 抗体)/C activity by interacting with Cdc20, and to result in aneuploidy development and genomic instability
porcine FZR1 (显示 FZR1 抗体) 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