Flt-4 Monoclonal Antibody

    • 货号:YM0279
    • 应用:WB;ELISA
    • 种属:Human
      • 靶点:
      • VEGFR3
      • 简介:
      • >>MAPK signaling pathway;>>Ras signaling pathway;>>Rap1 signaling pathway;>>Calcium signaling pathway;>>PI3K-Akt signaling pathway;>>Focal adhesion;>>Pathways in cancer;>>Breast cancer
      • 基因名称:
      • FLT4
      • 蛋白名称:
      • Vascular endothelial growth factor receptor 3
      • Human Gene Id:
      • 2324
      • Human Swiss Prot No:
      • P35916
      • Mouse Swiss Prot No:
      • P35917
      • 免疫原:
      • Purified recombinant fragment of human Flt-4 expressed in E. Coli.
      • 特异性:
      • Flt-4 Monoclonal Antibody detects endogenous levels of Flt-4 protein.
      • 组成:
      • Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
      • 来源:
      • Monoclonal, Mouse
      • 稀释:
      • WB 1:500 - 1:2000. ELISA: 1:10000. Not yet tested in other applications.
      • 纯化工艺:
      • Affinity purification
      • 储存:
      • -15°C to -25°C/1 year(Do not lower than -25°C)
      • 其他名称:
      • FLT4;VEGFR3;Vascular endothelial growth factor receptor 3;VEGFR-3;Fms-like tyrosine kinase 4;FLT-4;Tyrosine-protein kinase receptor FLT4
      • 分子量:
      • 153kD
      • 背景:
      • This gene encodes a tyrosine kinase receptor for vascular endothelial growth factors C and D. The protein is thought to be involved in lymphangiogenesis and maintenance of the lymphatic endothelium. Mutations in this gene cause hereditary lymphedema type IA. [provided by RefSeq, Jul 2008],
      • 功能:
      • catalytic activity:ATP + a [protein]-L-tyrosine = ADP + a [protein]-L-tyrosine phosphate.,disease:Defects in FLT4 are found in juvenile hemangioma. Juvenile hemangiomas are the most common tumors of infancy, occurring as many as 10% of all births. These benign vascular lesions enlarge rapidly during the first year of life by hyperplasia of endothelial cells and attendant pericytes, and then spontaneously involute over a period of years, leaving loose fibrofatty tissue.,disease:Defects in FLT4 are the cause of lymphedema hereditary type 1 (LYH1A) [MIM:153100]; also known as Nonne-Milroy lymphedema or Milroy disease. Hereditary lymphedema is a chronic disabling condition which results in swelling of the extremities due to altered lymphatic flow. Patients with lymphedema suffer from recurrent local infections and physical impairment.,function:Receptor for VEGFC. Has a tyrosine-protein kinas
      • 细胞定位:
      • Cell membrane ; Single-pass type I membrane protein. Cytoplasm . Nucleus . Ligand-mediated autophosphorylation leads to rapid internalization. .; [Isoform 1]: Cell membrane; Single-pass type I membrane protein. Ligand-mediated autophosphorylation leads to rapid internalization.; [Isoform 2]: Cell membrane; Single-pass type I membrane protein.; [Isoform 3]: Secreted. Cytoplasm.
      • 组织表达:
      • Detected in endothelial cells (at protein level). Widely expressed. Detected in fetal spleen, lung and brain. Detected in adult liver, muscle, thymus, placenta, lung, testis, ovary, prostate, heart, and kidney.
      • 产品图片
      • Western Blot analysis using Flt-4 Monoclonal Antibody against FLT4-hIgGFc transfected HEK293 cell lysate.