PENGARUH SUPLEMENTASI ESTRADIOL 17β TERHADAP PERSENTASE MATURASI IN VITRO OOSIT SAPI

This study aimed to determine the percentage of in vitro oocyte maturation on TCM – 199 media with estradiol 17ß supplementation. Cumulus oocyte complexes (COCs) that had been selected from the dissection media were added into the maturation media. The media was using TCM-19 which were added 0,15...

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Main Author: UMI MUFIDA, 061511133080
Format: Theses and Dissertations NonPeerReviewed
Language:Indonesian
Indonesian
Indonesian
Indonesian
Published: 2019
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Online Access:https://repository.unair.ac.id/87151/1/KKC%20KK%20KH%20235%20-%2019%20Muf%20p-Abstrak.pdf
https://repository.unair.ac.id/87151/2/KKC%20KK%20KH%20235%20-%2019%20Muf%20p-Daftar%20isi.pdf
https://repository.unair.ac.id/87151/3/KKC%20KK%20KH%20235%20-%2019%20Muf%20p-Daftar%20pustaka.pdf
https://repository.unair.ac.id/87151/4/KKC%20KK%20KH%20235%20-%2019%20Muf%20p.pdf
https://repository.unair.ac.id/87151/
http://lib.unair.ac.id
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spelling id-langga.871512023-11-29T04:42:13Z https://repository.unair.ac.id/87151/ PENGARUH SUPLEMENTASI ESTRADIOL 17β TERHADAP PERSENTASE MATURASI IN VITRO OOSIT SAPI UMI MUFIDA, 061511133080 Including veterinary genetics, ethology, anatomy, physiology, embryology, pathology This study aimed to determine the percentage of in vitro oocyte maturation on TCM – 199 media with estradiol 17ß supplementation. Cumulus oocyte complexes (COCs) that had been selected from the dissection media were added into the maturation media. The media was using TCM-19 which were added 0,15 IU/ml PMSG, 0,15 IU/ml HCG, FBS and estradiol 17ß. Each petridish contained three drops of maturation media (300 μl/drops) which were coated with mineral oil and then incubated in a 5% CO2 incubator, with maximum humidity and temperature of 39°C. Control (P0) was oocyte maturation without supplementation with the hormone estradiol 17ß supplementation 1μg/ml. Treatment 1 (P1) was oocyte maturation with 1μg/ml of estradiol 17ß supplementation. Treatment 2 (P2) was oocyte maturation with 2μg/ml of estradiol 17ß supplementation. The calculation of mature oocyte percentage was using aceto-orcein staining. The data analyzed using ANOVA, the result showed that there were no significant differences in control (P0) 50.63%, in treatment 2 (P2) 54.07%, and in treatment 3 (P3) 48.60%. Based on the result, it can be concluded that estradiol 17ß supplementation to the maturation level of cattle oocytes showed did not effect the percentage of in vitro oocyte maturation 2019 Thesis NonPeerReviewed text id https://repository.unair.ac.id/87151/1/KKC%20KK%20KH%20235%20-%2019%20Muf%20p-Abstrak.pdf text id https://repository.unair.ac.id/87151/2/KKC%20KK%20KH%20235%20-%2019%20Muf%20p-Daftar%20isi.pdf text id https://repository.unair.ac.id/87151/3/KKC%20KK%20KH%20235%20-%2019%20Muf%20p-Daftar%20pustaka.pdf text id https://repository.unair.ac.id/87151/4/KKC%20KK%20KH%20235%20-%2019%20Muf%20p.pdf UMI MUFIDA, 061511133080 (2019) PENGARUH SUPLEMENTASI ESTRADIOL 17β TERHADAP PERSENTASE MATURASI IN VITRO OOSIT SAPI. Skripsi thesis, UNIVERSITAS AIRLANGGA. http://lib.unair.ac.id
institution Universitas Airlangga
building Universitas Airlangga Library
continent Asia
country Indonesia
Indonesia
content_provider Universitas Airlangga Library
collection UNAIR Repository
language Indonesian
Indonesian
Indonesian
Indonesian
topic Including veterinary genetics, ethology, anatomy, physiology, embryology, pathology
spellingShingle Including veterinary genetics, ethology, anatomy, physiology, embryology, pathology
UMI MUFIDA, 061511133080
PENGARUH SUPLEMENTASI ESTRADIOL 17β TERHADAP PERSENTASE MATURASI IN VITRO OOSIT SAPI
description This study aimed to determine the percentage of in vitro oocyte maturation on TCM – 199 media with estradiol 17ß supplementation. Cumulus oocyte complexes (COCs) that had been selected from the dissection media were added into the maturation media. The media was using TCM-19 which were added 0,15 IU/ml PMSG, 0,15 IU/ml HCG, FBS and estradiol 17ß. Each petridish contained three drops of maturation media (300 μl/drops) which were coated with mineral oil and then incubated in a 5% CO2 incubator, with maximum humidity and temperature of 39°C. Control (P0) was oocyte maturation without supplementation with the hormone estradiol 17ß supplementation 1μg/ml. Treatment 1 (P1) was oocyte maturation with 1μg/ml of estradiol 17ß supplementation. Treatment 2 (P2) was oocyte maturation with 2μg/ml of estradiol 17ß supplementation. The calculation of mature oocyte percentage was using aceto-orcein staining. The data analyzed using ANOVA, the result showed that there were no significant differences in control (P0) 50.63%, in treatment 2 (P2) 54.07%, and in treatment 3 (P3) 48.60%. Based on the result, it can be concluded that estradiol 17ß supplementation to the maturation level of cattle oocytes showed did not effect the percentage of in vitro oocyte maturation
format Theses and Dissertations
NonPeerReviewed
author UMI MUFIDA, 061511133080
author_facet UMI MUFIDA, 061511133080
author_sort UMI MUFIDA, 061511133080
title PENGARUH SUPLEMENTASI ESTRADIOL 17β TERHADAP PERSENTASE MATURASI IN VITRO OOSIT SAPI
title_short PENGARUH SUPLEMENTASI ESTRADIOL 17β TERHADAP PERSENTASE MATURASI IN VITRO OOSIT SAPI
title_full PENGARUH SUPLEMENTASI ESTRADIOL 17β TERHADAP PERSENTASE MATURASI IN VITRO OOSIT SAPI
title_fullStr PENGARUH SUPLEMENTASI ESTRADIOL 17β TERHADAP PERSENTASE MATURASI IN VITRO OOSIT SAPI
title_full_unstemmed PENGARUH SUPLEMENTASI ESTRADIOL 17β TERHADAP PERSENTASE MATURASI IN VITRO OOSIT SAPI
title_sort pengaruh suplementasi estradiol 17β terhadap persentase maturasi in vitro oosit sapi
publishDate 2019
url https://repository.unair.ac.id/87151/1/KKC%20KK%20KH%20235%20-%2019%20Muf%20p-Abstrak.pdf
https://repository.unair.ac.id/87151/2/KKC%20KK%20KH%20235%20-%2019%20Muf%20p-Daftar%20isi.pdf
https://repository.unair.ac.id/87151/3/KKC%20KK%20KH%20235%20-%2019%20Muf%20p-Daftar%20pustaka.pdf
https://repository.unair.ac.id/87151/4/KKC%20KK%20KH%20235%20-%2019%20Muf%20p.pdf
https://repository.unair.ac.id/87151/
http://lib.unair.ac.id
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