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人 DPEP1 抗体对
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人 DPEP1 抗体对

01AB03302

Dipeptidase 1 (DPEP1) is a zinc-dependent metallodipeptidase and glycosylphosphatidylinositol-anchored membrane glycoprotein that forms disulfide-linked homodimers on the brush border of renal proximal tubules and other epithelia. It plays a central role in glutathione and leukotriene metabolism by hydrolyzing various dipeptides, notably converting leukotriene D4 to leukotriene E4. Additionally, DPEP1 acts as a neutrophil adhesion receptor, mediating leukocyte recruitment and inflammation in the kidneys, lungs, and liver. It is also the pharmacological target of cilastatin, which inhibits the hydrolysis of carbapenem antibiotics. Clinically, DPEP1 is significantly overexpressed in high-grade intraepithelial neoplasia and colorectal cancer, where it serves as an adverse prognostic marker and a potential diagnostic biomarker for tumor progression.

Human
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技术参数

靶点基因名
DPEP1
基因别名
MDP; RDP
蛋白别名
dipeptidase 1; DPEP1
UniProt
P16444
物种
Human

产品详情

靶点名称
DPEP1
蛋白名称
dipeptidase 1
蛋白别名
Dipeptidase 1; Beta-lactamase; Dehydropeptidase-I; Microsomal dipeptidase; Renal dipeptidase; hRDP
靶点基因名
DPEP1
基因别名
MDP; RDP
UniProt
P16444
来源物种
Homo sapiens (Human)
物种反应性
Human

背景介绍

Dipeptidase 1 (DPEP1) is a zinc-dependent metallodipeptidase and glycosylphosphatidylinositol-anchored membrane glycoprotein that forms disulfide-linked homodimers on the brush border of renal proximal tubules and other epithelia. It plays a central role in glutathione and leukotriene metabolism by hydrolyzing various dipeptides, notably converting leukotriene D4 to leukotriene E4. Additionally, DPEP1 acts as a neutrophil adhesion receptor, mediating leukocyte recruitment and inflammation in the kidneys, lungs, and liver. It is also the pharmacological target of cilastatin, which inhibits the hydrolysis of carbapenem antibiotics. Clinically, DPEP1 is significantly overexpressed in high-grade intraepithelial neoplasia and colorectal cancer, where it serves as an adverse prognostic marker and a potential diagnostic biomarker for tumor progression.