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dc.contributor.authorSaili, Takdir
dc.contributor.authorSetiadi, Mohamad Agus
dc.contributor.authorAgungpriyono, Srihadi
dc.contributor.authorBoediono, Arief
dc.date.accessioned2011-03-08T04:01:32Z
dc.date.available2011-03-08T04:01:32Z
dc.date.issued2007
dc.identifier.issn1411-8327-
dc.identifier.urihttp://repository.ipb.ac.id/handle/123456789/42595
dc.description.abstractIn ths experiment, the ability offeeeze-dried ram spermatozoa to decondense and to support pronucleus formation after injection into oocyte using ICSI method was evaluated. Aceto lacmoid staining was used to assess decondensation and pronucleus formation following ICSI.' Results of these experiments revealed that freeze-dried spermatozoa had the ability to decondense (2%) and to induce IPN formation (34%) following injection into oocytes but fail to form 2PN. However, 30% of 2PN and 40% oocytes were obtained when oocytes were injected with fresh spermatozoa. In conclusion, freeze-dried ram spermatozoa were able to decondense and to support 1PN formation after ICSI. Key words: spermatozoa, freeze-dried, oocyte, ICSI, decondensation, pronucleus.en
dc.publisherIPB (Bogor Agricultural University)
dc.titleInjeksi Spermatozoa Domba Hasil Pengeringbekuan ke dalam Sel Telur Menggunakan Teknik Intracytoplasmic Sperm Iw'ection (IC SI)en
dc.title.alternativeJurnal Veteriner Vol.8 No.1 Th.2007en
Appears in Collections:Media Veteriner

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