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dc.contributor.authorLan, C-C
dc.contributor.authorBlake, D
dc.contributor.authorHenry, S
dc.contributor.authorLove, D
dc.date.accessioned2012-03-11T20:49:53Z
dc.date.available2012-03-11T20:49:53Z
dc.date.copyright2012
dc.date.created2012
dc.date.issued2012-03-12
dc.identifier.citationIf you use this research data, please cite: Lan, C-C; Blake, D; Henry, S; Love, D. Fluorescent Function-Spacer-Lipid construct labeling allows for real-time in vivo imaging of cell migration and behaviour in zebrafish (Danio rerio). Journal of Fluorescence. July 2012, Volume 22, Issue 4, pp 1055-1063. DOI: http://dx.doi.org/10.1007/s10895-012-1043-3
dc.identifier.urihttp://hdl.handle.net/10292/3475
dc.description.abstractVideo descriptions: Video 1: 2 hours post injection imaging of the caudal vein plexus area of 52 hpf recipient zebrafish receiving 0.2 mg/ml FSL-FLRO4-I transformed WKM cells. In the video, a large slow-moving cell tumbles along the endothelial surface. Elongated oval shaped erythrocytes move at a fast speed. Video 2: Embryos (50-52hpf) were injected with 0.125 mg/ml FSL-FLRO4-II-treated cells. Window one focused on the eye region. Video 3: Embryos (50-52hpf) were injected with 0.125 mg/ml FSL-FLRO4-II-treated cells. Window two focused on the heart region. Video 4: Embryos (50-52hpf) were injected with 0.125 mg/ml FSL-FLRO4-II-treated cells. Window three focused on the first half the yolk extension region. Video 5: Embryos (50-52hpf) were injected with 0.125 mg/ml FSL-FLRO4-II-treated cells. Window four focused on the caudal half of the yolk extension and the anal regions. Video 6: Embryos (50-52hpf) were injected with 0.125 mg/ml FSL-FLRO4-II-treated cells. Window five focused on the caudal haematopoietic tissue region. Video 7: Embryos (50-52hpf) were injected with 0.125 mg/ml FSL-FLRO4-II-treated cells. Window six focused on the tail region. Video 8: Temporal assessment of FSL-FLRO4-II labeled cells in the lower trunk area. The image was taken 2 hours post injection for the sham-injected fish. Video 9: Temporal assessment of FSL-FLRO4-II labeled cells in the lower trunk area. The image was taken 2 hours post injection for the fish transplanted with FSL-FLRO4-II treated cells. Video 10: Temporal assessment of FSL-FLRO4-II labeled cells in the lower trunk area. The image was taken 19 hours post injection for the sham-injected fish. Video 11: Temporal assessment of FSL-FLRO4-II labeled cells in the lower trunk area. The image was taken 19 hours post injection for the fish transplanted with FSL-FLRO4-II treated cells. Video 12: Temporal assessment of FSL-FLRO4-II labeled cells in the lower trunk area. The image was taken 43 hours post injection for the sham-injected fish. Video 13: Temporal assessment of FSL-FLRO4-II labeled cells in the lower trunk area. The image was taken 43 hours post injection for the fish transplanted with FSL-FLRO4-II treated cells.en_NZ
dc.language.isoenen_NZ
dc.publisherAUT University
dc.relation.urihttp://dx.doi.org/10.1007/s10895-012-1043-3
dc.rightsAuckland University of Technology (AUT) encourages public access to AUT information and supports the legal use of copyright material in accordance with the Copyright Act 1994 (the Act) and the Privacy Act 1993. Unless otherwise stated, copyright material contained on this site may be in the intellectual property of AUT, a member of staff or third parties. Any commercial exploitation of this material is expressly prohibited without the written permission of the owner.
dc.titleVideos relating to Fluorescent Function-Spacer-Lipid construct labeling allows for real-time in vivo imaging of cell migration and behaviour in zebrafish (Danio rerio)en_NZ
dc.typeVideo
thesis.degree.grantorAUT University
thesis.degree.discipline
dc.date.updated2012-03-11T20:48:27Z


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