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Image / CIL:13677, Drosophila melanogaster, motor neuron

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Title
CIL:13677, Drosophila melanogaster, motor neuron
Creator
Bhat, Pavan
Collins, Catherine A
DiAntonio, Aaron
Ewanek, Ronny
Wang, Xin
Xiong, Xin
Contributor
Bhat, Pavan
Collins, Catherine A.
DiAntonio, Aaron
Ewanek, Ronny
Wang, Xin
Xiong, Xin
Date Created and/or Issued
2021
Contributing Institution
UC San Diego, Research Data Curation Program
Collection
Cell Image Library
Rights Information
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
The JNK phosphatase puckered, whose expression can be reported via a lacZ enhancer trap, is expressed in very low levels in uninjured neurons; however, nerve crush induces a dramatic increase in puc-lacZ expression in injured motoneurons. This image stack shows puc-lacZ (green) and neuronal nuclei (red) in a third instar larva injred at site 3 (as defined in Fig 1C). Wandering third instar larvae were dissected in PBS and fixed in either 4% paraformaldehyde in PBS or Bouin's fixative for 15–30 min. Primary antibodies used were: rat anti-elaV (7E8A10, Developmental Studies Hybridoma Bank) and mouse anti-lacZ (40-1a, DSHB). Secondary antibodies were Alexa 488 anti-mouse and Cy3 anti-rat. Confocal images were collected at room temperature on a spinning-disk confocal system (PerkinElmer) consisting of a scanner (Nipkow CSU10; Yokogawa) and an electron microscopy charge-coupled device camera (C9100-50; Hamamatsu Photonics) mounted on an inverted microscope (Axio Observer; Carl Zeiss, Inc.) with 25× 0.8 NA multi and 40× 1.3 NA, 63× 1.5 NA, and 100× 1.46 NA oil objectives. Similar settings were used to collect all compared genotypes. All imaging and quantification were conducted with Volocity software (PerkinElmer). This image stack corresponds to Fig 1E3 in J Cell Biol. 2010. 191: 211-223. Images in Fig 1 include CIL#s 13676, 13677, 13678, 13679.
Research Data Curation Program, UC San Diego, La Jolla, 92093-0175 (https://lib.ucsd.edu/rdcp)
Xiong, Xin; Wang, Xin; Ewanek, Ronny; Bhat, Pavan; DiAntonio, Aaron; Collins, Catherine A. (2021). CIL:13677, Drosophila melanogaster, motor neuron. In Cell Image Library. UC San Diego Library Digital Collections. Dataset. https://doi.org/10.6075/J0VQ31CX
Type
image
Identifier
ark:/20775/bb0962257x
Language
No linguistic content
Subject
RNA binding
JUN kinase phosphatase activity
Central nervous system development
Negative regulation of JNK cascade
JNK cascade
Negative regulation of mRNA 3'-end processing
Response to wounding
Motor neuron
Nucleus
Drosophila melanogaster
Cell Image Library Group ID: 7399

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