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the Aurora B (show AURKB ELISA Kits)-PLK1 (show PLK1 ELISA Kits) signaling at the kinetochore orchestrates MCAK activity, which is essential for timely correction of aberrant kinetochore attachment to ensure accurate chromosome segregation during mitosis.
MCAK activity is modulated by Plk1 (show PLK1 ELISA Kits) phosphorylation on S632/S633 in mitosis.
These results demonstrate that the structural change of Kif2C-ATP upon binding to microtubule ends is sufficient for tubulin (show TUBB ELISA Kits) release, whereas ATP hydrolysis is not required
Ras regulates KIF2C to control cell migration pathways in transformed human bronchial epithelial cells.
A dynamic interaction of MCAK-TIP150 orchestrated by Aurora A (show AURKA ELISA Kits)-mediated phosphorylation governs entosis via regulating microtubule plus-end dynamics and cell rigidity.
this study suggests a new mechanism by which Plk1 (show PLK1 ELISA Kits) regulates MCAK: by regulating its degradation and hence controlling its turnover in mitosis.
up-regulation of KIF2C and KIF2A by ERK1/2 caused aberrant lysosomal positioning and mTORC1 activity in a mutant K-Ras-dependent cancer and cancer model.
A Rac1-Aurora A (show AURKA ELISA Kits)-MCAK signaling pathway mediates endothelial cell polarization and directional migration by promoting regional differences in microtubule dynamics.
result suggested E403K mutation in mitotic centromere-associated kinesin protein (show KIF2B ELISA Kits) as highly damaging and showed strong concordance to the previously observed colorectal cancer mutations aggregation tendency and energy value changes
A CENP-E (show CENPE ELISA Kits) mediated wall-tethering event and a MCAK-mediated wall-removing event show that human chromosome-microtubule attachment is achieved through a set of deterministic sequential events rather than stochastic direct capture of microtubule ends.
PAK1 (show PAK1 ELISA Kits) phosphorylates MCAK and regulates both its localization and function.
MCAK appears to possess a unique distribution and function in oocyte maturation.
MCAK contributes to chromosome alignment in meiosis I, but is not necessary for preventing chromosome segregation errors.
Possible functions of MCAK at the inner centromere domain and at the perikinetochoric ring during both meiotic divisions.
Shugoshin 2 is necessary for the loading of MCAK at the inner centromere, but is dispensable for the loading of the outer kinetochore proteins BubR1 (show BUB1B ELISA Kits) and CENP-E (show CENPE ELISA Kits).
MCAK colocalized with NuMA (show NUMA1 ELISA Kits) and XMAP215 (show CKAP5 ELISA Kits) at the center of Ran asters where its activity is regulated by Aurora A (show AURKA ELISA Kits)-dependent phosphorylation of S196, which contributes to proper pole focusing
This study reveals a new role for Aurora B (show AURKB ELISA Kits), which is to prevent excess MCAK binding to chromatin to facilitate chromatin-nucleated spindle assembly.
MCAK regulation of cytoplasmic and spindle-associated (show HAUS1 ELISA Kits) microtubules can be differentiated by Aurora B (show AURKB ELISA Kits)-dependent phosphorylation
These data support a model in which Nup98 (show NUP98 ELISA Kits) interacts with microtubules and antagonizes MCAK activity, thus promoting bipolar spindle assembly.
The protein encoded by this gene is a member of kinesin-like protein family. Proteins of this family are microtubule-dependent molecular motors that transport organelles within cells and move chromosomes during cell division. This protein is important for anaphase chromosome segregation and may be required to coordinate the onset of sister centromere separation.
kinesin family member 2C
, kinesin-like protein KIF2C
, kinesin-like protein KIF2C-like
, kinesin-like 6
, kinesin-like protein 6
, mitotic centromere-associated kinesin
, kinesin-related protein 2
, Kinesin-like protein 6
, kinesin central motor 1