Under copyright Constraint(s) on Use: This work is protected by the U.S. Copyright Law (Title 17, U.S.C.). Use of this work beyond that allowed by "fair use" or any license applied to this work requires written permission of the copyright holder(s). Responsibility for obtaining permissions and any use and distribution of this work rests exclusively with the user and not the UC San Diego Library. Inquiries can be made to the UC San Diego Library program having custody of the work. Use: This work is available from the UC San Diego Library. This digital copy of the work is intended to support research, teaching, and private study.
Rights Holder and Contact
UC Regents
Description
A time lapse experiment of Saccharomyces cerevisiae expressing GFP-tagged TEM1. TEM1 is a GTP-binding protein of the ras superfamily involved in termination of M-phase; controls actomyosin and septin dynamics during cytokinesis. These phase,gfp z-series images are part of an image group that ranges from CIL:39591-39595. Note that there are additional groups showing time series of other cell cycle regulation proteins by the same authors in the Library. Research Data Curation Program, UC San Diego, La Jolla, 92093-0175 (https://lib.ucsd.edu/rdcp) Ball, David; Peccoud, Jean (2021). CIL:39591, Saccharomyces cerevisiae. In Cell Image Library. UC San Diego Library Digital Collections. Dataset. https://doi.org/10.6075/J0C829DG
Type
image
Identifier
ark:/20775/bb84720732
Language
No linguistic content
Subject
Cell division Small GTPase mediated signal transduction Nucleotide binding Mitosis GTPase activity Cell cycle Regulation of exit from mitosis GTP binding Protein binding Spindle pole body TEM1 protein Saccharomyces cerevisiae Cell Image Library Group ID: 10632
If you're wondering about permissions and what you can do with this item, a good starting point is the "rights information" on this page. See our terms of use for more tips.
Share your story
Has Calisphere helped you advance your research, complete a project, or find something meaningful? We'd love to hear about it; please send us a message.
