Xenopus chip for single-egg trapping, in vitro fertilization, development, and tadpole escape

Cited 3 time in scopus
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dc.contributor.authorS W Nam-
dc.contributor.authorJ P Chae-
dc.contributor.authorY H Kwon-
dc.contributor.authorMi-Young Son-
dc.contributor.authorJ S Bae-
dc.contributor.authorM J Park-
dc.date.accessioned2021-07-08T03:30:21Z-
dc.date.available2021-07-08T03:30:21Z-
dc.date.issued2021-
dc.identifier.issn0006-291X-
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/24469-
dc.description.abstractXenopus laevis is highly suitable as a toxicology animal model owing to its advantages in embryogenesis research. For toxicological studies, a large number of embryos must be handled simultaneously because they very rapidly develop into the target stages within a short period of time. To efficiently handle the embryos, a convenient embryo housing device is essential for fast and reliable assessment and statistical evaluation of malformation caused by toxicants. Here, we suggest 3D fabrication of single-egg trapping devices in which Xenopus eggs are fertilized in vitro, and the embryos are cultured. We used manual pipetting to insert the Xenopus eggs inside the trapping sites of the chip. By introducing a liquid circulating system, we connected a sperm-mixed solution with the chip to induce in vitro fertilization of the eggs. After the eggs were fertilized, we observed embryo development involving the formation of egg cleavage, blastula, gastrula, and tadpole. After the tadpoles grew inside the chip, we saved their lives by enabling their escape from the chip through reverse flow of the culture medium. The Xenopus chip can serve as an incubator to induce fertilization and monitor normal and abnormal development of the Xenopus from egg to tadpole.-
dc.publisherElsevier-
dc.titleXenopus chip for single-egg trapping, in vitro fertilization, development, and tadpole escape-
dc.title.alternativeXenopus chip for single-egg trapping, in vitro fertilization, development, and tadpole escape-
dc.typeArticle-
dc.citation.titleBiochemical and Biophysical Research Communications-
dc.citation.number0-
dc.citation.endPage34-
dc.citation.startPage29-
dc.citation.volume569-
dc.contributor.affiliatedAuthorMi-Young Son-
dc.contributor.alternativeName남성욱-
dc.contributor.alternativeName채정필-
dc.contributor.alternativeName권용환-
dc.contributor.alternativeName손미영-
dc.contributor.alternativeName배재성-
dc.contributor.alternativeName박매자-
dc.identifier.bibliographicCitationBiochemical and Biophysical Research Communications, vol. 569, pp. 29-34-
dc.identifier.doi10.1016/j.bbrc.2021.06.049-
dc.subject.keywordXenopus laevis-
dc.subject.keywordEmbryogenesis-
dc.subject.keywordIn vitro fertilization-
dc.subject.keywordBiochip-
dc.subject.keywordTadpole trapping-
dc.subject.localXenopus laevis-
dc.subject.localEmbryogenesis-
dc.subject.localembryogenesis-
dc.subject.localIn vitro fertilization-
dc.subject.localin vitro fertilisation-
dc.subject.localin vitro fertilization-
dc.subject.localBiochip-
dc.subject.localbiochip-
dc.subject.localTadpole trapping-
dc.description.journalClassY-
Appears in Collections:
Division of Research on National Challenges > Stem Cell Convergenece Research Center > 1. Journal Articles
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