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anti-Human KIF2C Antikörper:
anti-Mouse (Murine) KIF2C Antikörper:
anti-Rat (Rattus) KIF2C Antikörper:
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Human Polyclonal KIF2C Primary Antibody für IP, WB - ABIN251028
Pakala, Nair, Reddy, Kumar: Signaling-dependent phosphorylation of mitotic centromere-associated kinesin regulates microtubule depolymerization and its centrosomal localization. in The Journal of biological chemistry 2012
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Human Monoclonal KIF2C Primary Antibody für IF, IHC (p) - ABIN564770
Sanhaji, Friel, Kreis, Krämer, Martin, Howard, Strebhardt, Yuan: Functional and spatial regulation of mitotic centromere-associated kinesin by cyclin-dependent kinase 1. in Molecular and cellular biology 2010
Show all 2 Pubmed References
Authors find that 3D ECM engagement uncouples MCAK-mediated regulation of MT growth persistence from myosin-II-mediated regulation of growth persistence specifically within EC branched protrusions.
REVIEW: Conformation changes in MCAK related to its depolymerization activity and function are described. A model of its regulation by multiple mitotic kinases is proposed and its potential involvement in oncogenesis and drug resistance its highlighted.
GTSE1 (zeige GTSE1 Antikörper) inhibition of MCAK activity regulates the balance of MT stability that determines the fidelity of chromosome alignment, segregation, and chromosomal stability.
MCAC (zeige SLC25A20 Antikörper) role in microtubule assembly
Our results reveal an underlying mechanism by which NuSAP (zeige NUSAP1 Antikörper) controls kinetochore microtubule dynamics spatially and temporally by modulating the depolymerisation function of MCAK in an Aurora B kinase (zeige AURKB Antikörper)-dependent manner.
MCAK is involved in directional migration and invasion of tumor cells.
the Aurora B (zeige AURKB Antikörper)-PLK1 (zeige PLK1 Antikörper) 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 (zeige PLK1 Antikörper) 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 (zeige TUBB Antikörper) release, whereas ATP hydrolysis is not required
Ras regulates KIF2C to control cell migration pathways in transformed human bronchial epithelial cells.
PAK1 (zeige PAK1 Antikörper) 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 (zeige SGOL2 Antikörper) is necessary for the loading of MCAK at the inner centromere, but is dispensable for the loading of the outer kinetochore proteins BubR1 (zeige BUB1B Antikörper) and CENP-E (zeige CENPE Antikörper).
MCAK colocalized with NuMA (zeige NUMA1 Antikörper) and XMAP215 (zeige CKAP5 Antikörper) at the center of Ran asters where its activity is regulated by Aurora A (zeige AURKA Antikörper)-dependent phosphorylation of S196, which contributes to proper pole focusing
This study reveals a new role for Aurora B (zeige AURKB Antikörper), which is to prevent excess MCAK binding to chromatin to facilitate chromatin-nucleated spindle assembly.
MCAK regulation of cytoplasmic and spindle-associated (zeige HAUS1 Antikörper) microtubules can be differentiated by Aurora B (zeige AURKB Antikörper)-dependent phosphorylation
These data support a model in which Nup98 (zeige NUP98 Antikörper) 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