PD-ECGF Polyclonal Antibody

    • 货号:YT5414
    • 应用:WB;IHC;IF;ELISA
    • 种属:Human;Rat;Mouse;
      • 靶点:
      • PD-ECGF
      • 简介:
      • >>Pyrimidine metabolism;>>Drug metabolism - other enzymes;>>Metabolic pathways;>>Nucleotide metabolism;>>Bladder cancer
      • 基因名称:
      • TYMP
      • 蛋白名称:
      • Thymidine phosphorylase
      • Human Gene Id:
      • 1890
      • Human Swiss Prot No:
      • P19971
      • Mouse Swiss Prot No:
      • Q99N42
      • 免疫原:
      • The antiserum was produced against synthesized peptide derived from the N-terminal region of human TYMP. AA range:11-60
      • 特异性:
      • PD-ECGF Polyclonal Antibody detects endogenous levels of PD-ECGF protein.
      • 组成:
      • Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
      • 来源:
      • Polyclonal, Rabbit,IgG
      • 稀释:
      • WB 1:500 - 1:2000. IHC: 1:100-1:300. ELISA: 1:20000.. IF 1:50-200
      • 纯化工艺:
      • The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
      • 浓度:
      • 1 mg/ml
      • 储存:
      • -15°C to -25°C/1 year(Do not lower than -25°C)
      • 其他名称:
      • TYMP;ECGF1;Thymidine phosphorylase;TP;Gliostatin;Platelet-derived endothelial cell growth factor;PD-ECGF;TdRPase
      • 实测条带:
      • 50kD
      • 背景:
      • This gene encodes an angiogenic factor which promotes angiogenesis in vivo and stimulates the in vitro growth of a variety of endothelial cells. It has a highly restricted target cell specificity acting only on endothelial cells. Mutations in this gene have been associated with mitochondrial neurogastrointestinal encephalomyopathy. Multiple alternatively spliced transcript variants have been identified. [provided by RefSeq, Apr 2012],
      • 功能:
      • catalytic activity:Thymidine + phosphate = thymine + 2-deoxy-alpha-D-ribose 1-phosphate.,disease:Defects in TYMP are the cause of mitochondrial neurogastrointestinal encephalomyopathy (MNGIE) [MIM:603041]; also known as myoneurogastrointestinal encephalomyopathy. MNGIE is an autosomal recessive disease associated with multiple deletions of skeletal muscle mitochondrial DNA (MtDNA). It is clinically characterized by onset between the second and fifth decades of life, ptosis, progressive external ophthalmoplegia, gastrointestinal dysmotility (often pseudoobstruction), diffuse leukoencephalopathy, thin body habitus, peripheral neuropathy, and myopathy.,function:Catalyzes the reversible phosphorolysis of thymidine. The produced molecules are then utilized as carbon and energy sources or in the rescue of pyrimidine bases for nucleotide synthesis.,function:May have a role in maintaining the in
      • 细胞定位:
      • cytosol,
      • 组织表达:
      • Brain,Lung,Placenta,Synovial membrane tissue,
      • 产品图片
      • Western Blot analysis of MCF-7, 293 cells using PD-ECGF Polyclonal Antibody. Secondary antibody(catalog#:RS0002) was diluted at 1:20000
      • Immunohistochemical analysis of paraffin-embedded Human kidney. 1, Antibody was diluted at 1:200(4° overnight). 2, High-pressure and temperature EDTA, pH8.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 30min).
      • Western blot analysis of lysate from 293, MCF-7 cells, using TYMP Antibody.