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eBioscience 14-0443-82 Affinity Purified anti-mouse Lyve-1 (Lymphatic Vessel En

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产品名称: eBioscience 14-0443-82 Affinity Purified anti-mouse Lyve-1 (Lymphatic Vessel En
产品型号: 14-0443-82
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eBioscience 14-0443-82 Affinity Purified anti-mouse Lyve-1 (Lymphatic Vessel Endothelial Receptor 1)


eBioscience 14-0443-82 Affinity Purified anti-mouse Lyve-1 (Lymphatic Vessel En  的详细介绍
eBioscience 14-0443-82 Affinity Purified anti-mouse Lyve-1 (Lymphatic Vessel Endothelial Receptor 1)

产品名称:Affinity Purified anti-mouse Lyve-1 (Lymphatic Vessel Endothelial Receptor 1) 100 ug
产品货号:eBioscience 14-0443-82
产品规格:100 ug
Anti-Mouse Lyve-1 Purified
Also known as: Lymphatic Vessel Endothelial Hyaluronan Receptor 1, Cell surface retention sequence-binding protein 1, CRSBP-1, Extracellular link domain-containing protein 1, Hyaluronic acid receptor
Clone: ALY7
RUO: For Research Use Only. Not for use in diagnostic procedures.
SKU# 14-0443
Cat. No. Size
14-0443-80  25 ug 
14-0443-82  100 ug 
Description: The monoclonal antibody ALY7 recognizes mouse LYVE-1, a transmembrane glycoprotein with similarity to CD44. The extracellular domain contains a conserved hyaluronan binding domain also found in CD44. Expression is found on lymphatic and liver endothelial cells and some populations of macrophages. The lymphatic system is responsible for transporting proteins and cells (especially dendritic cells) to tissues throughout the body, thereby acting as immune surveyors. LYVE-1 is one characteristic protein, along with podoplanin, PROX-1, Tie-2 and VEGFR-3, that is expressed on lymphatic endothelial cells (LECS). The ligand for LYVE-1 is hyaluronan, a large mucopolysaccharide. Although LYVE-1 can bind hyaluronan in vitro, the site for ligand binding in vivo is masked by sialyated O-linked glycan chains. It is postulated that binding to ligand requires modification/unmasking to expose the binding site. The development and remodeling of the endothelium after injury is an area of extensive study. When transplanted, hematopoietic stem cells (HSCs) can give rise to LECs that integrate into the endothelium in normal and metastatic tissue.
 

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