Literature DB >> 21357130

Construction of a Heated Incubation Chamber around a Microscope Stage for Time-Lapse Imaging.

Paul M Kulesa1, Jennifer C Kasemeier-Kulesa.   

Abstract

INTRODUCTIONIntravital imaging of embryogenesis has the potential to provide valuable information on cell proliferation, cell shape changes, and cell migratory behaviors. However, most embryo model systems require a temperature-controlled environment. Several expensive commercially available temperature control devices have emerged, including microscope stages surrounded by custom-fit Plexiglas boxes, heated plates for culture dishes, and objective warmers for water-immersion lenses, that strictly control temperature and, in some cases, help control local gas mixtures. This protocol describes an easy-to-assemble, cost-effective, custom-made cardboard box and incubator, adaptable to each user's specifications and microscope set-up. The cardboard box fits around the microscope, primarily the stage area, to assist in maintaining a prescribed temperature near the microscope stage. Warmed air, blown into the box enclosure from an incubator, circulates around the stage. The heated incubation box maintains a set temperature with minimal fluctuations and has been tested and utilized for studies of chick, mouse, and zebrafish embryogenesis.

Entities:  

Year:  2007        PMID: 21357130     DOI: 10.1101/pdb.prot4792

Source DB:  PubMed          Journal:  CSH Protoc        ISSN: 1559-6095


  8 in total

1.  Neural crest invasion is a spatially-ordered progression into the head with higher cell proliferation at the migratory front as revealed by the photoactivatable protein, KikGR.

Authors:  Paul M Kulesa; Jessica M Teddy; Danny A Stark; Sarah E Smith; Rebecca McLennan
Journal:  Dev Biol       Date:  2008-02-07       Impact factor: 3.582

2.  An introduction to the wound healing assay using live-cell microscopy.

Authors:  James E N Jonkman; Judith A Cathcart; Feng Xu; Miria E Bartolini; Jennifer E Amon; Katarzyna M Stevens; Pina Colarusso
Journal:  Cell Adh Migr       Date:  2014       Impact factor: 3.405

3.  Automated Multichamber Time-lapse Videography for Long-term In Vivo Observation of Migrating Cells.

Authors:  Helmut Buhler; Raphael Adamietz; Theresa Abeln; David Diaz-Carballo; Pascaline Nguemgo-Kouam; Thomas Hero; Irenaus A Adamietz
Journal:  In Vivo       Date:  2017 May-Jun       Impact factor: 2.155

4.  In ovo live imaging of avian embryos.

Authors:  Paul M Kulesa; Caleb M Bailey; Cameron Cooper; Scott E Fraser
Journal:  Cold Spring Harb Protoc       Date:  2010-06

5.  Multi-position photoactivation and multi-time acquisition for large-scale cell tracing in avian embryos.

Authors:  Joseph Steen; Jason A Morrison; Paul M Kulesa
Journal:  Cold Spring Harb Protoc       Date:  2010-06

Review 6.  Could time-lapse embryo imaging reduce the need for biopsy and PGS?

Authors:  Jason E Swain
Journal:  J Assist Reprod Genet       Date:  2013-07-11       Impact factor: 3.412

7.  Capturing tissue repair in zebrafish larvae with time-lapse brightfield stereomicroscopy.

Authors:  Thomas S Lisse; Elizabeth A Brochu; Sandra Rieger
Journal:  J Vis Exp       Date:  2015-01-31       Impact factor: 1.355

8.  TrkB/BDNF signalling patterns the sympathetic nervous system.

Authors:  Jennifer C Kasemeier-Kulesa; Jason A Morrison; Frances Lefcort; Paul M Kulesa
Journal:  Nat Commun       Date:  2015-09-25       Impact factor: 14.919

  8 in total

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