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抗人 EPS8L1 抗体对
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抗人 EPS8L1 抗体对

01AB02407

EPS8 signaling adaptor L1 (EPS8L1) is a cytoplasmic adaptor protein that modulates Ras signaling and actin cytoskeleton remodeling. As a member of the EPS8 family, it stimulates the guanine nucleotide exchange activity of SOS1, facilitating membrane ruffling and structural changes. EPS8L1 is involved in the maintenance of epidermal and hair follicle barrier structures. Clinically, variants in the EPS8L1 gene are associated with Fetal Akinesia Deformation Sequence 4, a severe congenital neuromuscular disorder. It has also been linked to villous adenocarcinoma and pathways relevant to Fragile X syndrome. These associations underscore the importance of EPS8L1 in developmental signaling and its potential role in tumorigenesis through the regulation of cytoskeletal dynamics.

Human
规格起售价
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技术参数

靶点基因名
EPS8L1
基因别名
DRC3; EPS8R1
蛋白别名
EPS8 signaling adaptor L1; EPS8L1
UniProt
Q8TE68
物种
Human

产品详情

靶点名称
EPS8L1
蛋白名称
EPS8 signaling adaptor L1
蛋白别名
Epidermal growth factor receptor kinase substrate 8-like protein 1; EPS8-like protein 1; Epidermal growth factor receptor pathway substrate 8-related protein 1; EPS8-related protein 1
靶点基因名
EPS8L1
基因别名
DRC3; EPS8R1
UniProt
Q8TE68
来源物种
Homo sapiens (Human)
物种反应性
Human

背景介绍

EPS8 signaling adaptor L1 (EPS8L1) is a cytoplasmic adaptor protein that modulates Ras signaling and actin cytoskeleton remodeling. As a member of the EPS8 family, it stimulates the guanine nucleotide exchange activity of SOS1, facilitating membrane ruffling and structural changes. EPS8L1 is involved in the maintenance of epidermal and hair follicle barrier structures. Clinically, variants in the EPS8L1 gene are associated with Fetal Akinesia Deformation Sequence 4, a severe congenital neuromuscular disorder. It has also been linked to villous adenocarcinoma and pathways relevant to Fragile X syndrome. These associations underscore the importance of EPS8L1 in developmental signaling and its potential role in tumorigenesis through the regulation of cytoskeletal dynamics.