MTHFR Monoclonal Antibody

    • 货号:YM0455
    • 应用:WB;IHC;IF;ELISA
    • 种属:Human;Rat
      • 靶点:
      • MTHFR
      • 简介:
      • >>One carbon pool by folate;>>Metabolic pathways;>>Antifolate resistance
      • 基因名称:
      • MTHFR
      • 蛋白名称:
      • Methylenetetrahydrofolate reductase
      • Human Gene Id:
      • 4524
      • Human Swiss Prot No:
      • P42898
      • Mouse Swiss Prot No:
      • Q9WU20
      • 免疫原:
      • Purified recombinant fragment of human MTHFR expressed in E. Coli.
      • 特异性:
      • MTHFR Monoclonal Antibody detects endogenous levels of MTHFR 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. IHC 1:200 - 1:1000. ELISA: 1:10000.. IF 1:50-200
      • 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:
      • MTHFR;Methylenetetrahydrofolate reductase
      • 分子量:
      • 75kD
      • 背景:
      • The protein encoded by this gene catalyzes the conversion of 5,10-methylenetetrahydrofolate to 5-methyltetrahydrofolate, a co-substrate for homocysteine remethylation to methionine. Genetic variation in this gene influences susceptibility to occlusive vascular disease, neural tube defects, colon cancer and acute leukemia, and mutations in this gene are associated with methylenetetrahydrofolate reductase deficiency.[provided by RefSeq, Oct 2009],
      • 功能:
      • catalytic activity:5-methyltetrahydrofolate + NAD(P)(+) = 5,10-methylenetetrahydrofolate + NAD(P)H.,cofactor:FAD.,disease:Defects in MTHFR are the cause of methylenetetrahydrofolate reductase deficiency (MTHFRD) [MIM:236250]. MTHFRD is autosomal recessive disorder with a wide range of features including homocysteinuria, homocysteinemia [MIM:603174], developmental delay, severe mental retardation, perinatal death, psychiatric disturbances, and later-onset neurodegenerative disorders.,disease:Defects in MTHFR may be a cause of susceptibility to folate-sensitive neural tube defects (folate-sensitive NTD) [MIM:601634]. The most common NTDs are open spina bifida (myelomeningocele) and anencephaly.,disease:Defects in MTHFR may be a cause of susceptibility to ischemic stroke [MIM:601367]; also known as cerebrovascular accident or cerebral infarction. A stroke is an acute neurologic event leadin
      • 细胞定位:
      • cytosol,synapse,
      • 组织表达:
      • Brain,Liver,Lung,
      • 产品图片
      • Western Blot analysis using MTHFR Monoclonal Antibody against HEK293 (1) and MTHFR-hIgGFc transfected HEK293 (2) cell lysate.
      • Immunohistochemistry analysis of paraffin-embedded lung cancer tissues with DAB staining using MTHFR Monoclonal Antibody.