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抗人 SBNO1 抗体对
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抗人 SBNO1 抗体对

01AB01332

Strawberry notch homolog 1 (SBNO1) is a nuclear protein and member of the SF2 family, which includes DExD/H box helicases and Swi2/Snf2 chromatin remodelers, and is predicted to enable chromatin DNA and histone binding activities. SBNO1 plays a key role in transcriptional regulation, particularly by stimulating the activity of transcription factors such as Yap/Tead4 and Notch/Rbpj, and is essential for the activation of specific gene enhancers like Cdx2 during early embryonic development. It is involved in the regulation of neural stem cell proliferation, enhancing GSK3B phosphorylation through the PI3K-Akt signaling pathway, and is exclusively localized in the nucleus throughout development. Disruption of SBNO1 in mouse models leads to embryonic arrest at the preimplantation stage due to loss of trophectoderm-specific gene expression, highlighting its critical developmental role; in humans, altered SBNO1 expression has been observed in glioblastoma, suggesting a potential link to disease.

Human
规格起售价
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技术参数

靶点基因名
SBNO1
基因别名
MOP3
蛋白别名
strawberry notch homolog 1; SBNO1
UniProt
A3KN83
物种
Human

产品详情

靶点名称
SBNO1
蛋白名称
strawberry notch homolog 1
蛋白别名
Protein strawberry notch homolog 1; Monocyte protein 3; MOP-3
靶点基因名
SBNO1
基因别名
MOP3
UniProt
A3KN83
来源物种
Homo sapiens (Human)
物种反应性
Human

背景介绍

Strawberry notch homolog 1 (SBNO1) is a nuclear protein and member of the SF2 family, which includes DExD/H box helicases and Swi2/Snf2 chromatin remodelers, and is predicted to enable chromatin DNA and histone binding activities. SBNO1 plays a key role in transcriptional regulation, particularly by stimulating the activity of transcription factors such as Yap/Tead4 and Notch/Rbpj, and is essential for the activation of specific gene enhancers like Cdx2 during early embryonic development. It is involved in the regulation of neural stem cell proliferation, enhancing GSK3B phosphorylation through the PI3K-Akt signaling pathway, and is exclusively localized in the nucleus throughout development. Disruption of SBNO1 in mouse models leads to embryonic arrest at the preimplantation stage due to loss of trophectoderm-specific gene expression, highlighting its critical developmental role; in humans, altered SBNO1 expression has been observed in glioblastoma, suggesting a potential link to disease.