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Development of two-cell mouse embryos in protein-free and protein-supplemented media.

作者信息

Dandekar P V, Glass R H

机构信息

Department of Obstetrics, Gynecology and Reproductive Sciences, University of California, San Francisco 94143.

出版信息

J In Vitro Fert Embryo Transf. 1990 Apr;7(2):107-13. doi: 10.1007/BF01135584.

DOI:10.1007/BF01135584
PMID:2358725
Abstract

Two-cell mouse embryos from CFW (Swiss-Webster) mice were cultured to the blastocyst stage in Ham's F10, Whittingham's T6, or human tubal fluid medium. Media were used without any protein supplements or were supplemented with human maternal serum, human fetal cord serum, or human serum albumin. Blastocysts were transferred to modified Eagle's basal medium supplemented with 10% fetal bovine serum for postblastocyst development. Blastocyst and postblastocyst development was depressed among embryos cultured during the preimplantation stage in protein-free Whittingham's T6 and human tubal fluid media compared with embryos cultured in protein-free Ham's F10 medium. This advantage of Ham's F10 disappeared when amino acids and vitamins were added to the other two media. Whittingham's T6 and human tubal fluid supplemented with human serum albumin, human maternal serum, or human fetal cord serum also supported excellent embryo development. When supplemented with protein, Ham's F10 was the poorest of the media in supporting embryo development. Although these results suggest that Ham's F10 is not the best medium for culture of mouse embryos, there is need for caution in extrapolating results from the mouse to the human.

摘要

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本文引用的文献

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A METHOD FOR IN VITRO CULTIVATION OF MOUSE OVA FROM TWO-CELL TO BLASTOCYST.一种将小鼠卵从二细胞培养至囊胚的体外培养方法。
Exp Cell Res. 1963 Oct;32:205-8. doi: 10.1016/0014-4827(63)90093-4.
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