Protocol for odorant-binding protein 2A gene knockdown by dual siRNA transfection in a three-dimensional human epidermal equivalent model.

IF 1.3 Q4 BIOCHEMICAL RESEARCH METHODS STAR Protocols Pub Date : 2025-03-21 Epub Date: 2025-02-05 DOI:10.1016/j.xpro.2025.103626
Shinobu Nakanishi
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Abstract

Gene knockdown by small interfering RNA (siRNA) transfection is widely used to investigate gene function. Here, we present a protocol for the knockdown of the odorant-binding protein 2A (OBP2A) gene in a three-dimensional human epidermal equivalent model (3DE-model). We describe steps for growing human epidermal keratinocytes (normal human epithelial keratinocytes [NHEKs]) for 3DE-model construction in monolayer culture. We then detail procedures for transfecting the cells with siRNA, followed by a second siRNA transfection during 3DE-model construction. The efficiency of gene knockdown is verified by qPCR and ELISA. For complete details on the use and execution of this protocol, please refer to Nakanishi et al.1.

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双siRNA转染在三维人表皮等效模型中敲除气味结合蛋白2A基因的方案。
小干扰RNA (small interfering RNA, siRNA)转染基因敲低被广泛用于研究基因功能。在这里,我们提出了一个在三维人类表皮等效模型(3de模型)中敲除气味结合蛋白2A (OBP2A)基因的方案。我们描述了在单层培养中培养用于构建3de模型的人表皮角质形成细胞(正常人上皮角质形成细胞[NHEKs])的步骤。然后,我们详细介绍了用siRNA转染细胞的程序,随后在3de模型构建期间进行第二次siRNA转染。qPCR和ELISA验证了基因敲低的有效性。有关本协议使用和执行的完整细节,请参考Nakanishi等人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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