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人 CXCL2 抗体对
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人 CXCL2 抗体对

01AB03100

C-X-C motif chemokine ligand 2 (CXCL2) is a secreted ELR+ CXC chemokine, also known as GRO-beta or MIP-2-alpha, primarily produced by activated monocytes, macrophages, and various stromal cells. It functions as a potent chemoattractant for neutrophils and other polymorphonuclear leukocytes by binding to the G protein-coupled receptor CXCR2. This interaction triggers downstream signaling pathways that induce cytoskeletal remodeling, cell migration, and adhesion. CXCL2 plays a critical role in orchestrating leukocyte recruitment during acute inflammation and contributes to wound healing and antimicrobial defense. Pathologically, dysregulated CXCL2-CXCR2 signaling is implicated in obesity-associated adipose tissue inflammation, stroke-related brain infiltration, and various chronic inflammatory diseases. In oncology, it promotes tumor proliferation, angiogenesis, and metastasis.

Human
规格起售价
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技术参数

靶点基因名
CXCL2
基因别名
GRO2; GROB; MIP2A; SCYB2
蛋白别名
C-X-C motif chemokine ligand 2; CXCL2
UniProt
P19875
物种
Human

产品详情

靶点名称
CXCL2
蛋白名称
C-X-C motif chemokine ligand 2
蛋白别名
C-X-C motif chemokine 2; Growth-regulated protein beta; Gro-beta; Macrophage inflammatory protein 2-alpha; MIP2-alpha) [Cleaved into: GRO-beta(5-73; GRO-beta-T; Hematopoietic synergistic factor; HSF; SB-251353]
靶点基因名
CXCL2
基因别名
GRO2; GROB; MIP2A; SCYB2
UniProt
P19875
来源物种
Homo sapiens (Human)
物种反应性
Human

背景介绍

C-X-C motif chemokine ligand 2 (CXCL2) is a secreted ELR+ CXC chemokine, also known as GRO-beta or MIP-2-alpha, primarily produced by activated monocytes, macrophages, and various stromal cells. It functions as a potent chemoattractant for neutrophils and other polymorphonuclear leukocytes by binding to the G protein-coupled receptor CXCR2. This interaction triggers downstream signaling pathways that induce cytoskeletal remodeling, cell migration, and adhesion. CXCL2 plays a critical role in orchestrating leukocyte recruitment during acute inflammation and contributes to wound healing and antimicrobial defense. Pathologically, dysregulated CXCL2-CXCR2 signaling is implicated in obesity-associated adipose tissue inflammation, stroke-related brain infiltration, and various chronic inflammatory diseases. In oncology, it promotes tumor proliferation, angiogenesis, and metastasis.