TY - CHAP
T1 - Manipulating and Imaging the Early Xenopus laevis Embryo
AU - Danilchik, Michael V.
N1 - Funding Information:
Danilchik’s research is supported by the National Science Foundation (IOS-0921415).
Publisher Copyright:
© 2011, Springer Science+Business Media, LLC.
PY - 2011
Y1 - 2011
N2 - Over the past half century, the Xenopus laevis embryo has become a popular model system for studying vertebrate early development at molecular, cellular, and multicellular levels. The year-round availability of easily fertilized eggs, the embryo’s large size and rapid development, and the hardiness of both adults and offspring against a wide range of laboratory conditions provide unmatched advantages for a variety of approaches, particularly “cutting and pasting” experiments, to explore embryogenesis. There is, however, a common perception that the Xenopus embryo is intractable for microscope work, due to its store of large, refractile yolk platelets and abundant cortical pigmentation. This chapter presents easily adapted protocols to surmount, and in some cases take advantage of, these optical properties to facilitate live-cell microscopic analysis of commonly used experimental manipulations of early Xenopus embryos.
AB - Over the past half century, the Xenopus laevis embryo has become a popular model system for studying vertebrate early development at molecular, cellular, and multicellular levels. The year-round availability of easily fertilized eggs, the embryo’s large size and rapid development, and the hardiness of both adults and offspring against a wide range of laboratory conditions provide unmatched advantages for a variety of approaches, particularly “cutting and pasting” experiments, to explore embryogenesis. There is, however, a common perception that the Xenopus embryo is intractable for microscope work, due to its store of large, refractile yolk platelets and abundant cortical pigmentation. This chapter presents easily adapted protocols to surmount, and in some cases take advantage of, these optical properties to facilitate live-cell microscopic analysis of commonly used experimental manipulations of early Xenopus embryos.
KW - Xenopus laevis
KW - cytoskeleton
KW - dorsal–ventral axis
KW - embryo
KW - live-cell confocal imaging
KW - time-lapse microscopy
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U2 - 10.1007/978-1-61779-210-6_2
DO - 10.1007/978-1-61779-210-6_2
M3 - Chapter
C2 - 21805260
AN - SCOPUS:80052944945
SN - 9781617792090
T3 - Methods in Molecular Biology
SP - 21
EP - 54
BT - Vertebrate Embryogenesis
PB - Humana Press Inc.
ER -