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人 LRRN1 抗体对
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人 LRRN1 抗体对

01AB00297

Leucine rich repeat neuronal 1 (LRRN1) is a protein encoded by the LRRN1 gene in humans. It is a single-pass, transmembrane protein characterized by leucine-rich repeats, which are known to be involved in various cellular processes including cell-cell interactions and signaling pathways. LRRN1 has been implicated in several biological processes, including the regulation of boundary formation and cellular patterning during development, particularly in the organ of Corti in the mammalian cochlea. It interacts with the Notch signaling pathway to enhance Notch activity, which is crucial for the proper formation of sensory and nonsensory regions in the cochlea. Additionally, LRRN1 has been associated with the suppression of apoptosis in gastric cancer cells through the regulation of Fas/FasL. Its role in neuroblastoma and neuronal development as an extracellular negative regulator of ALK signaling has also been noted.

Human
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技术参数

靶点基因名
LRRN1
基因别名
KIAA1497
蛋白别名
leucine rich repeat neuronal 1; LRRN1
UniProt
Q6UXK5
物种
Human

产品详情

靶点名称
LRRN1
蛋白名称
leucine rich repeat neuronal 1
蛋白别名
Leucine-rich repeat neuronal protein 1; Neuronal leucine-rich repeat protein 1; NLRR-1
靶点基因名
LRRN1
基因别名
KIAA1497
UniProt
Q6UXK5
来源物种
Homo sapiens (Human)
物种反应性
Human

背景介绍

Leucine rich repeat neuronal 1 (LRRN1) is a protein encoded by the LRRN1 gene in humans. It is a single-pass, transmembrane protein characterized by leucine-rich repeats, which are known to be involved in various cellular processes including cell-cell interactions and signaling pathways. LRRN1 has been implicated in several biological processes, including the regulation of boundary formation and cellular patterning during development, particularly in the organ of Corti in the mammalian cochlea. It interacts with the Notch signaling pathway to enhance Notch activity, which is crucial for the proper formation of sensory and nonsensory regions in the cochlea. Additionally, LRRN1 has been associated with the suppression of apoptosis in gastric cancer cells through the regulation of Fas/FasL. Its role in neuroblastoma and neuronal development as an extracellular negative regulator of ALK signaling has also been noted.