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人 FGF1 抗体对
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人 FGF1 抗体对

01AB03469

Fibroblast growth factor 1 (FGF1), also called acidic FGF, is a heparin-binding growth factor encoded by the FGF1 gene and produced as a 155–amino acid polypeptide that yields a nonglycosylated protein of about 17–18 kDa. It acts mainly as a potent mitogen and survival factor, regulating cell proliferation, differentiation, migration, and angiogenesis through binding to fibroblast growth factor receptors (especially FGFR1) in a heparan-sulfate–dependent manner and activating downstream MAPK/ERK and PI3K–AKT signaling cascades. FGF1 is expressed in many tissues, can signal both extracellularly and within the nucleus, and participates in processes such as embryonic development, tissue repair, and bone formation. Pathologically, dysregulated FGF1 signaling contributes to tumor growth and invasion, while in metabolism it modulates adipose and hepatic glucose handling and has shown the ability to normalize blood glucose in diabetic mouse models.

Human
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技术参数

靶点基因名
FGF1
基因别名
FGFA
蛋白别名
fibroblast growth factor 1; FGF1
UniProt
P05230
物种
Human

产品详情

靶点名称
FGF1
蛋白名称
fibroblast growth factor 1
蛋白别名
Fibroblast growth factor 1; FGF-1; Acidic fibroblast growth factor; aFGF; Endothelial cell growth factor; ECGF; Heparin-binding growth factor 1; HBGF-1
靶点基因名
FGF1
基因别名
FGFA
UniProt
P05230
来源物种
Homo sapiens (Human)
物种反应性
Human

背景介绍

Fibroblast growth factor 1 (FGF1), also called acidic FGF, is a heparin-binding growth factor encoded by the FGF1 gene and produced as a 155–amino acid polypeptide that yields a nonglycosylated protein of about 17–18 kDa. It acts mainly as a potent mitogen and survival factor, regulating cell proliferation, differentiation, migration, and angiogenesis through binding to fibroblast growth factor receptors (especially FGFR1) in a heparan-sulfate–dependent manner and activating downstream MAPK/ERK and PI3K–AKT signaling cascades. FGF1 is expressed in many tissues, can signal both extracellularly and within the nucleus, and participates in processes such as embryonic development, tissue repair, and bone formation. Pathologically, dysregulated FGF1 signaling contributes to tumor growth and invasion, while in metabolism it modulates adipose and hepatic glucose handling and has shown the ability to normalize blood glucose in diabetic mouse models.