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原肠胚期小鼠胚胎的体外培养。

The in vitro culture of primitive-streak-stage mouse embryos.

作者信息

Tam P P, Snow M H

出版信息

J Embryol Exp Morphol. 1980 Oct;59:131-43.

PMID:7217867
Abstract

The in vitro growth and morphogenesis of mouse embryos from early primitive-streak stage to early-somite stage is described. The embryo culture method employs a static culture system, a conventional chemically defined medium (Dulbecco's modified Eagle's medium), supplemented with additional glucose, glutamine and suitably prepared serum. The method of serum preparation is important for successful culture. Both mouse serum and rat serum support good development of primitive-streak-stage mouse embryos. Over 60% of early-streak stage and about 90% of late-streak stage grow and develop for 48 h in vitro. During the first 24 h in culture, total growth of the embryos as reflected by protein content, size and morphology is the same as in vivo.

摘要

本文描述了小鼠胚胎从早期原条阶段到早期体节阶段的体外生长和形态发生。胚胎培养方法采用静态培养系统,即一种常规的化学成分明确的培养基(杜氏改良 Eagle 培养基),并添加了额外的葡萄糖、谷氨酰胺和经过适当制备的血清。血清制备方法对于成功培养至关重要。小鼠血清和大鼠血清都能支持原条阶段小鼠胚胎的良好发育。超过60%的早期原条阶段胚胎和约90%的晚期原条阶段胚胎在体外生长发育48小时。在培养的最初24小时内,胚胎的总体生长情况,如通过蛋白质含量、大小和形态所反映的,与体内情况相同。

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