Summary of ssbd-repos-000123

SSBD:database
URL

Name
ssbd-repos-000123 (123-Yalikun-ZygoteDyn)
URL
DOI
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Title
Living image of capturing the whole surface of a mouse zygote during rotation
Description
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Submited Date
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Release Date
2019-11-20
Updated Date
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License
Funding information
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File formats
Data size
542.3 MB

Organism
M. musculus
Strain
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Cell Line
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Genes
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Proteins
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GO Molecular Function (MF)
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GO Biological Process (BP)
Fertilization
GO Cellular Component (CC)
NA
Study Type
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Imaging Methods
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Method Summary
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Related paper(s)

Yalikun, Yaxiaer, Aishan, Yusufu, Mosha, Abulaiti, Sumiyama, Kenta, Tanaka, Yo (2018), Oocyte all-surfaces’ imaging method using micro-scale rotational flow, Micro & Nano Letters, Volume 13, Number 3, 306-311

Published in 2018/03/01

(Abstract) In this work, the authors report an all-surfaces? image capturing method of a single oocyte that uses micro-scale rotational flow. Here, the authors used this method gently and indirectly rotated the single pronuclear zygotes (physical properties are similar to those of oocytes) to obtain images of all its surfaces in 0.33 s. The necessary equipment to realise this method consists of only a syringe pump and a microfluidic chip with a single 40 µm diameter orifice. Assessment of viability and quality of oocytes or embryos during the process of intra cytoplasmic sperm injection) and in vitro fertilisation is important for good embryo development. At present, manual morphological evaluation is the most common method to assess viability and quality of oocytes. Usually, during the manual morphological evaluation, the operator is required to manipulate the oocyte to achieve its full surface image. However, manipulation is difficult, even for an experienced operator. Conventional methods using the principles of mechanics, electronics, or magnetism require a complex system. Conventional methods using principles of fluids or optics also have limitations about target size and transparency. Here, a method is proposed and proved of using rotational flow to gently capture and rotate a mouse zygote without using a complex control system and achieved its full surface image in 0.33 s. The method offers a new tool for morphological evaluation of assessment of viability and quality of oocytes.

Contact(s)
Yo Tanaka, Yaxiaer Yalikun
Organization(s)
RIKEN , Center for Biosystems Dynamics Research , Laboratory for Integrated Biodevice
Image Data Contributors
Quantitative Data Contributors

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