CN205170866U - No clear tape embryo culture ware - Google Patents
No clear tape embryo culture ware Download PDFInfo
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- CN205170866U CN205170866U CN201521006018.9U CN201521006018U CN205170866U CN 205170866 U CN205170866 U CN 205170866U CN 201521006018 U CN201521006018 U CN 201521006018U CN 205170866 U CN205170866 U CN 205170866U
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- 210000001161 mammalian embryo Anatomy 0.000 title abstract description 16
- 210000002257 embryonic structure Anatomy 0.000 claims description 15
- 210000004340 zona pellucida Anatomy 0.000 abstract description 13
- 230000008901 benefit Effects 0.000 abstract description 4
- 230000018109 developmental process Effects 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- 230000013020 embryo development Effects 0.000 description 3
- 239000012531 culture fluid Substances 0.000 description 2
- 238000012136 culture method Methods 0.000 description 2
- 238000000338 in vitro Methods 0.000 description 2
- 238000010449 nuclear transplantation Methods 0.000 description 2
- 206010068051 Chimerism Diseases 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- 239000005662 Paraffin oil Substances 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 210000002459 blastocyst Anatomy 0.000 description 1
- 238000003776 cleavage reaction Methods 0.000 description 1
- 238000012258 culturing Methods 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 235000013601 eggs Nutrition 0.000 description 1
- 239000001963 growth medium Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 210000000056 organ Anatomy 0.000 description 1
- 230000008672 reprogramming Effects 0.000 description 1
- 230000007017 scission Effects 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 230000009261 transgenic effect Effects 0.000 description 1
- 238000002054 transplantation Methods 0.000 description 1
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- Apparatus Associated With Microorganisms And Enzymes (AREA)
Abstract
本实用新型提供一种无透明带胚胎培养皿,它包括有培养皿盖和培养皿体,培养皿体底部直径为90mm,培养皿体壁厚为3mm,培养皿体底部设有若干个培养腔,培养腔为沉孔,相邻培养腔的间距为0.4cm,均匀分布于培养皿体底板上。本实用新型的优点在于结构简单、规格标准化、可以实现规模化培养。
The utility model provides an embryo culture dish without zona pellucida, which includes a culture dish cover and a culture dish body, the bottom diameter of the culture dish body is 90 mm, the wall thickness of the culture dish body is 3 mm, and several culture chambers are arranged at the bottom of the culture dish body , the culture chambers are countersunk holes, and the distance between adjacent culture chambers is 0.4cm, which are evenly distributed on the bottom plate of the culture dish. The utility model has the advantages of simple structure, standardized specifications, and large-scale cultivation can be realized.
Description
技术领域 technical field
本实用新型涉及无透明带胚胎培养装置,更具体的说,涉及一种可以进行无透明带胚胎体外培养皿。 The utility model relates to a zona-free embryo culture device, in particular to an in vitro culture dish for zona-free embryos.
背景技术 Background technique
传统的核移植是在透明带完整的基础上进行的,因为传统观点认为透明带对于核重新编程及胚胎的后续发育是必须的。利用传统方法进行核移植研究时,需要昂贵的仪器设备,同时要求操作者掌握熟练的技术,从而限制了核移植研究,特别是应用的发展。但是,最近的研究表明透明带并非胚胎发育所必需。有学者发现无透明带的受精卵能发育至囊胚。但是进行无透明带核移植研究还是面临一大难题:无透明带胚胎在培养时易聚集,不适合于传统集中培养。为此,单个胚胎培养系统的研究显得十分必要。 The traditional nuclear transfer is carried out on the basis of the integrity of the zona pellucida, because the traditional view is that the zona pellucida is necessary for nuclear reprogramming and the subsequent development of the embryo. When using traditional methods to conduct nuclear transfer research, expensive instruments and equipment are required, and operators are required to master skilled techniques, which limits nuclear transfer research, especially the development of applications. However, recent studies have shown that the zona pellucida is not required for embryonic development. Some scholars have found that fertilized eggs without zona pellucida can develop into blastocysts. However, research on zona-free nuclear transfer still faces a major problem: zona-free embryos tend to aggregate during culture and are not suitable for traditional concentrated culture. Therefore, the research on single embryo culture system is very necessary.
单个胚胎培养系统是随着无透明带核移植技术的发展也发展起来的一种胚胎培养方式,而且只有单个胚胎在里面进行培养。现有传统的单个胚胎培养方法操作复杂,效率不高,同时无法让多个培养的胚胎在培养的过程中发生联系,无法发挥传统胚胎集中培养的优势(集中培养胚胎分泌的因子相互调节促进胚胎发育)。 The single embryo culture system is an embryo culture method developed with the development of zona-free nuclear transfer technology, and only a single embryo is cultured in it. The existing traditional single embryo culture method is complex and inefficient, and at the same time cannot allow multiple cultured embryos to be connected during the culture process, and cannot take advantage of the traditional centralized culture of embryos (the factors secreted by concentrated cultured embryos regulate each other to promote embryo development). development).
发明内容 Contents of the invention
本实用新型的目的是提供了一种无透明带胚胎培养皿进行胚胎的集中下的分离单个培养,来克服无透明带胚胎集中培养容易发生粘附的问题,同时也有利于单个胚胎的卵裂球之间的粘附,从而提高透明带胚胎体外培养效率。 The purpose of this utility model is to provide a non-zona pellucida embryo culture dish for centralized separation and individual culture of embryos, to overcome the problem of easy adhesion of non-zona pellucida embryos in centralized culture, and also to facilitate the cleavage of single embryos Adhesion between balls, thereby improving the efficiency of in vitro culture of zona pellucida embryos.
为实现上述目的,本实用新型所提供的技术方案为:一种无透明带胚胎培养皿,它包括有培养皿盖和培养皿体,培养皿体底部直径为90mm,培养皿体壁厚为3mm,培养皿体底部设有若干个培养腔,培养腔为沉孔,相邻培养腔的间距为0.4cm,均匀分布于培养皿体底板上。 In order to achieve the above object, the technical scheme provided by the utility model is: a culture dish without zona pellucida, which includes a culture dish cover and a culture dish body, the diameter of the bottom of the culture dish body is 90mm, and the wall thickness of the culture dish body is 3mm , There are several culture cavities at the bottom of the culture dish, the culture chambers are countersunk holes, the distance between adjacent culture chambers is 0.4cm, and they are evenly distributed on the bottom plate of the culture dish.
所述的培养腔深度为1000um,直径为400um。 The culture chamber has a depth of 1000um and a diameter of 400um.
所述的培养皿体底部设有方形的培养区,培养腔位于培养区内。 The bottom of the culture dish is provided with a square culture area, and the culture chamber is located in the culture area.
本实用新型的有益效果: The beneficial effects of the utility model:
第一、结构简单,方便进行无透明带胚胎培养操作。 First, the structure is simple, and it is convenient to carry out the operation of culturing embryos without zona pellucida.
第二、该装置节省材料、节省培养液,易于被广大研究者接受。 Second, the device saves materials and culture fluid, and is easy to be accepted by researchers.
第三、规格标准化,可以实现规模化,提高其经济效益。 Third, standardization of specifications can achieve scale and improve its economic benefits.
第四、由于属于一次性耗材,具有很大的市场应用价值。 Fourth, because it is a disposable consumable, it has great market application value.
附图说明 Description of drawings
图1为本实用新型的整体结构示意图。 Figure 1 is a schematic diagram of the overall structure of the utility model.
具体实施方式 detailed description
下面结合所有附图对本实用新型作进一步说明,本实用新型的较佳实施为:参见附图1,本实施例所述的无透明带胚胎培养皿包括有培养皿盖2和培养皿体1,培养皿体1底部直径为90mm,培养皿体1壁厚为3mm,培养皿体1底部设有若干个可容纳125.6ul体积培养液的培养腔3,培养腔3为沉孔,培养腔3深度为1000um,直径为400um,相邻培养腔3的间距为0.4cm,均匀分布于培养皿体1底板上。还可以根据需要在培养皿体1底部设有方形的培养区4,培养腔3位于培养区内。本培养皿可有效使得无透明带胚胎进行集中培养液下的单独培养,能够有效防止无透明带胚胎的相互粘附,使无透明带胚胎培养更简单,更有效率。由于无透明带核移植与传统核移植相比,不仅不需要昂贵的仪器设备,而且其工作强度和操作技术难度也降低了许多。同时,无透明带核移植有独特的优势,如进行胚胎嵌合的研究。这为今后无透明带核移植技术的研究与推广应用奠定了扎实的基础,同时由于转基因动物或异种器官移植需要进行无透明带核移植技术,所以无透明带胚胎培养皿的应用具有很大的市场潜力。在实际应用中,在培养皿中加入平胚胎培养液,然后盖石蜡油,接着可以用移胚管吸取当个的无透明带胚胎每个孔中放入一个胚胎。这样就形成了无透明带胚胎单个培养的集中培养体系,从而提高胚胎发育的效率。 Below in conjunction with all accompanying drawings, the utility model is further described, and the preferred implementation of the utility model is: referring to accompanying drawing 1, the culture dish without zona pellucida described in the present embodiment includes a culture dish cover 2 and a culture dish body 1, The diameter of the bottom of the culture dish body 1 is 90mm, and the wall thickness of the culture dish body 1 is 3mm. The bottom of the culture dish body 1 is provided with several culture chambers 3 that can accommodate 125.6ul of culture fluid. The culture chamber 3 is a sink hole, and the depth of the culture chamber 3 is The diameter is 1000um, the diameter is 400um, the distance between adjacent culture chambers 3 is 0.4cm, and they are evenly distributed on the bottom plate of the culture dish body 1 . A square culture area 4 can also be provided at the bottom of the culture dish body 1 as required, and the culture cavity 3 is located in the culture area. The culture dish can effectively enable the zona-free embryos to be cultured separately under concentrated culture solution, can effectively prevent the mutual adhesion of the zona-free embryos, and makes the culture of the zona-free embryos simpler and more efficient. Compared with traditional nuclear transplantation, zone-free nuclear transplantation not only does not require expensive instruments and equipment, but also reduces the work intensity and technical difficulty of operation. At the same time, zona-free nuclear transfer has unique advantages, such as the study of embryo chimerism. This has laid a solid foundation for the research and application of zona-free nuclear transfer technology in the future. At the same time, since transgenic animals or xenogeneic organ transplantation require zona-free nuclear transfer technology, the application of zona-free embryo culture dishes has great potential. Market potential. In practical application, add flat embryo culture medium in the petri dish, then cover with paraffin oil, then you can use the embryo transfer tube to suck up the current embryo without zona pellucida and put one embryo in each well. In this way, a centralized culture system for single culture of embryos without zona pellucida is formed, thereby improving the efficiency of embryo development.
以上所述之实施例只为本实用新型之较佳实施例,并非以此限制本实用新型的实施范围,故凡依本实用新型之形状、原理所作的变化,均应涵盖在本实用新型的保护范围内。 The above-described embodiments are only preferred embodiments of the present utility model, and are not intended to limit the scope of implementation of the present utility model, so all changes made according to the shape and principle of the present utility model should be covered by the scope of the present utility model. within the scope of protection.
Claims (3)
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CN201521006018.9U CN205170866U (en) | 2015-12-08 | 2015-12-08 | No clear tape embryo culture ware |
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CN201521006018.9U CN205170866U (en) | 2015-12-08 | 2015-12-08 | No clear tape embryo culture ware |
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Cited By (11)
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US11345880B2 (en) | 2017-07-14 | 2022-05-31 | Corning Incorporated | 3D cell culture vessels for manual or automatic media exchange |
US11441121B2 (en) | 2013-04-30 | 2022-09-13 | Corning Incorporated | Spheroid cell culture article and methods thereof |
US11584906B2 (en) | 2017-07-14 | 2023-02-21 | Corning Incorporated | Cell culture vessel for 3D culture and methods of culturing 3D cells |
US11613722B2 (en) | 2014-10-29 | 2023-03-28 | Corning Incorporated | Perfusion bioreactor platform |
US11661574B2 (en) | 2018-07-13 | 2023-05-30 | Corning Incorporated | Fluidic devices including microplates with interconnected wells |
US11732227B2 (en) | 2018-07-13 | 2023-08-22 | Corning Incorporated | Cell culture vessels with stabilizer devices |
US11767499B2 (en) | 2017-07-14 | 2023-09-26 | Corning Incorporated | Cell culture vessel |
US11857970B2 (en) | 2017-07-14 | 2024-01-02 | Corning Incorporated | Cell culture vessel |
US11912968B2 (en) | 2018-07-13 | 2024-02-27 | Corning Incorporated | Microcavity dishes with sidewall including liquid medium delivery surface |
US11976263B2 (en) | 2014-10-29 | 2024-05-07 | Corning Incorporated | Cell culture insert |
US12203059B2 (en) | 2014-10-29 | 2025-01-21 | Corning Incorporated | Microwell design and fabrication for generation of cell culture aggregates |
-
2015
- 2015-12-08 CN CN201521006018.9U patent/CN205170866U/en not_active Expired - Fee Related
Cited By (15)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US11441121B2 (en) | 2013-04-30 | 2022-09-13 | Corning Incorporated | Spheroid cell culture article and methods thereof |
US12146154B2 (en) | 2013-04-30 | 2024-11-19 | Corning Incorporated | Spheroid cell culture article and methods thereof |
US11976263B2 (en) | 2014-10-29 | 2024-05-07 | Corning Incorporated | Cell culture insert |
US11613722B2 (en) | 2014-10-29 | 2023-03-28 | Corning Incorporated | Perfusion bioreactor platform |
US12203059B2 (en) | 2014-10-29 | 2025-01-21 | Corning Incorporated | Microwell design and fabrication for generation of cell culture aggregates |
US11667874B2 (en) | 2014-10-29 | 2023-06-06 | Corning Incorporated | Perfusion bioreactor platform |
US11584906B2 (en) | 2017-07-14 | 2023-02-21 | Corning Incorporated | Cell culture vessel for 3D culture and methods of culturing 3D cells |
US11345880B2 (en) | 2017-07-14 | 2022-05-31 | Corning Incorporated | 3D cell culture vessels for manual or automatic media exchange |
US11767499B2 (en) | 2017-07-14 | 2023-09-26 | Corning Incorporated | Cell culture vessel |
US11857970B2 (en) | 2017-07-14 | 2024-01-02 | Corning Incorporated | Cell culture vessel |
US11970682B2 (en) | 2017-07-14 | 2024-04-30 | Corning Incorporated | 3D cell culture vessels for manual or automatic media exchange |
US11732227B2 (en) | 2018-07-13 | 2023-08-22 | Corning Incorporated | Cell culture vessels with stabilizer devices |
US11912968B2 (en) | 2018-07-13 | 2024-02-27 | Corning Incorporated | Microcavity dishes with sidewall including liquid medium delivery surface |
US11661574B2 (en) | 2018-07-13 | 2023-05-30 | Corning Incorporated | Fluidic devices including microplates with interconnected wells |
US12270017B2 (en) | 2018-07-13 | 2025-04-08 | Corning Incorporated | Cell culture vessels with stabilizer devices |
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