人胚泡中磷酸化SMAD蛋白的免疫荧光检测和定量方法。

IF 1.3 Q4 BIOCHEMICAL RESEARCH METHODS
Todd Fallesen, A Sophie Brumm
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引用次数: 0

摘要

转化生长因子β (TGF-β)信号超家族包括NODAL和骨形态发生蛋白(BMP)信号,它们导致不同SMAD蛋白的磷酸化并调节关键的发育事件。在这里,我们提出了一种在植入前人类胚胎中磷酸化SMAD蛋白与其他转录因子结合的免疫荧光检测方案。我们描述了在人类囊胚中分割细胞核和定量其免疫荧光强度的步骤。该方案可适用于其他哺乳动物胚胎或其体外发育模型中TGF-β超家族信号活性的研究。有关本协议使用和执行的完整细节,请参阅Brumm等人1。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Protocol for immunofluorescence detection and quantification of phosphorylated SMAD proteins in human blastocysts.

The transforming growth factor β (TGF-β) signaling superfamily includes NODAL and bone morphogenetic protein (BMP) signaling, which lead to the phosphorylation of different SMAD proteins and regulate key developmental events. Here, we present a protocol for immunofluorescence detection of phosphorylated SMAD proteins combined with other transcription factors in pre-implantation human embryos. We describe steps for segmenting the nuclei in human blastocysts and quantifying their immunofluorescence intensity. This protocol can be adapted to investigate TGF-β superfamily signaling activity in other mammalian embryos or in vitro models of their development. For complete details on the use and execution of this protocol, please refer to Brumm et al.1.

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来源期刊
STAR Protocols
STAR Protocols Biochemistry, Genetics and Molecular Biology-General Biochemistry, Genetics and Molecular Biology
CiteScore
2.00
自引率
0.00%
发文量
789
审稿时长
10 weeks
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