The utilization of separate culture chambers serves a dual purpose: it not only facilitates the creation of a hypoxic environment but also contributes to the establishment of a consistently stable local environment. This, in turn, mitigates environmental stress factors. The primary objective of this experiment was to assess the developmental potential of sheep embryos before their implantation. This assessment was conducted within the confines of 304 stainless steel culture chambers, offering a viable alternative for maintaining a stable in vitro embryo culture environment. The experiment involved a comparative analysis between the development outcomes of parthenogenetic and reconstituted sheep embryos cultured in both stainless steel tanks or MIC-101 incubators over a period of 7 days. Notably, the blastocyst rates for parthenogenetic embryos were 26.45% and 24.84% in stainless steel tanks and MIC-101 incubators, respectively, with no statistically significant difference (P>0.05) between them. Similarly, the blastocyst rates for reconstituted embryos stood at 16.07% and 16.84% (P>0.05) for stainless steel tanks and MIC-101 incubators, respectively. It is worth highlighting that the incubation system, comprising a 304 stainless steel tank, a standard gas mixture, and a thermostat, presents an in vitro culture system with the advantages of cost-effectiveness, environmental stability, and efficacy.
Published in | International Journal of Animal Science and Technology (Volume 7, Issue 3) |
DOI | 10.11648/j.ijast.20230703.12 |
Page(s) | 43-47 |
Creative Commons |
This is an Open Access article, distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution and reproduction in any medium or format, provided the original work is properly cited. |
Copyright |
Copyright © The Author(s), 2023. Published by Science Publishing Group |
Incubator, In Vitro Culture, Embryo, Sheep
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APA Style
Feng Guangyu, Xiang Chunhe, Wang Limin, Zhou Ping, Pi Wenhui. (2023). Effect of Stainless Steel Tank Incubation System on Development of Ovine Embryos. International Journal of Animal Science and Technology, 7(3), 43-47. https://doi.org/10.11648/j.ijast.20230703.12
ACS Style
Feng Guangyu; Xiang Chunhe; Wang Limin; Zhou Ping; Pi Wenhui. Effect of Stainless Steel Tank Incubation System on Development of Ovine Embryos. Int. J. Anim. Sci. Technol. 2023, 7(3), 43-47. doi: 10.11648/j.ijast.20230703.12
AMA Style
Feng Guangyu, Xiang Chunhe, Wang Limin, Zhou Ping, Pi Wenhui. Effect of Stainless Steel Tank Incubation System on Development of Ovine Embryos. Int J Anim Sci Technol. 2023;7(3):43-47. doi: 10.11648/j.ijast.20230703.12
@article{10.11648/j.ijast.20230703.12, author = {Feng Guangyu and Xiang Chunhe and Wang Limin and Zhou Ping and Pi Wenhui}, title = {Effect of Stainless Steel Tank Incubation System on Development of Ovine Embryos}, journal = {International Journal of Animal Science and Technology}, volume = {7}, number = {3}, pages = {43-47}, doi = {10.11648/j.ijast.20230703.12}, url = {https://doi.org/10.11648/j.ijast.20230703.12}, eprint = {https://article.sciencepublishinggroup.com/pdf/10.11648.j.ijast.20230703.12}, abstract = {The utilization of separate culture chambers serves a dual purpose: it not only facilitates the creation of a hypoxic environment but also contributes to the establishment of a consistently stable local environment. This, in turn, mitigates environmental stress factors. The primary objective of this experiment was to assess the developmental potential of sheep embryos before their implantation. This assessment was conducted within the confines of 304 stainless steel culture chambers, offering a viable alternative for maintaining a stable in vitro embryo culture environment. The experiment involved a comparative analysis between the development outcomes of parthenogenetic and reconstituted sheep embryos cultured in both stainless steel tanks or MIC-101 incubators over a period of 7 days. Notably, the blastocyst rates for parthenogenetic embryos were 26.45% and 24.84% in stainless steel tanks and MIC-101 incubators, respectively, with no statistically significant difference (P>0.05) between them. Similarly, the blastocyst rates for reconstituted embryos stood at 16.07% and 16.84% (P>0.05) for stainless steel tanks and MIC-101 incubators, respectively. It is worth highlighting that the incubation system, comprising a 304 stainless steel tank, a standard gas mixture, and a thermostat, presents an in vitro culture system with the advantages of cost-effectiveness, environmental stability, and efficacy.}, year = {2023} }
TY - JOUR T1 - Effect of Stainless Steel Tank Incubation System on Development of Ovine Embryos AU - Feng Guangyu AU - Xiang Chunhe AU - Wang Limin AU - Zhou Ping AU - Pi Wenhui Y1 - 2023/10/14 PY - 2023 N1 - https://doi.org/10.11648/j.ijast.20230703.12 DO - 10.11648/j.ijast.20230703.12 T2 - International Journal of Animal Science and Technology JF - International Journal of Animal Science and Technology JO - International Journal of Animal Science and Technology SP - 43 EP - 47 PB - Science Publishing Group SN - 2640-1312 UR - https://doi.org/10.11648/j.ijast.20230703.12 AB - The utilization of separate culture chambers serves a dual purpose: it not only facilitates the creation of a hypoxic environment but also contributes to the establishment of a consistently stable local environment. This, in turn, mitigates environmental stress factors. The primary objective of this experiment was to assess the developmental potential of sheep embryos before their implantation. This assessment was conducted within the confines of 304 stainless steel culture chambers, offering a viable alternative for maintaining a stable in vitro embryo culture environment. The experiment involved a comparative analysis between the development outcomes of parthenogenetic and reconstituted sheep embryos cultured in both stainless steel tanks or MIC-101 incubators over a period of 7 days. Notably, the blastocyst rates for parthenogenetic embryos were 26.45% and 24.84% in stainless steel tanks and MIC-101 incubators, respectively, with no statistically significant difference (P>0.05) between them. Similarly, the blastocyst rates for reconstituted embryos stood at 16.07% and 16.84% (P>0.05) for stainless steel tanks and MIC-101 incubators, respectively. It is worth highlighting that the incubation system, comprising a 304 stainless steel tank, a standard gas mixture, and a thermostat, presents an in vitro culture system with the advantages of cost-effectiveness, environmental stability, and efficacy. VL - 7 IS - 3 ER -