S-Trityl-L-cysteine
Catalog # 2191 | Tocris Bioscience a Bio-Techne Brand
Potent, selective inhibitor of mitotic kinesin Eg5
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Key Product Details
Description: | Potent, selective inhibitor of mitotic kinesin Eg5 |
Alternative Names: | NSC 83265 |
Chemical Name: | S-(Triphenylmethyl)-L-cysteine |
Molecular Weight: | 363.47 |
Citations for S-Trityl-L-cysteine (6)
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Citations are publications that use Bio-Techne products. Selected citations for S-Trityl-L-cysteine include:
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Cilibrasi et al.
(2019)
A Ploidy Increase Promotes Sensitivity of Glioma Stem Cells to Aurora Kinases Inhibition.
J Oncol.
2019:9014045
PMID: 31531022 -
Ferreira et al.
(2018)
Dissecting the role of the tubulin code in mitosis.
Methods Cell Biol.
144:33
PMID: 29804676 -
Hengeveld
(2017)
Inner centromere localization of the CPC maintains centromere cohesion and allows mitoticcheckpoint silencing.
Nat Commun.
8:15542
PMID: 28561035 -
Hindriksen et al.
(2017)
Baculoviral delivery of CRISPR/Cas9 facilitates efficient genome editing in human cells.
PLoS One.
12:e0179514
PMID: 28640891 -
Müllers et al.
(2014)
Nuclear translocation of Cyclin B1 marks the restriction point for terminal cell cycle exit in G2 phase.
PLoS Genet.
13:2733
PMID: 25486360 -
Hégarat et al.
(2014)
PP2A/B55 and Fcp1 regulate Greatwall and Ensa dephosphorylation during mitotic exit.
J Pharmacol Exp Ther.
10:e1004004
PMID: 24391510
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