D3DR Polyclonal Antibody

    • 货号:YT5448
    • 应用:WB;ELISA
    • 种属:Human;Mouse;Rat
      • 靶点:
      • D3DR
      • 简介:
      • >>Neuroactive ligand-receptor interaction;>>Dopaminergic synapse
      • 基因名称:
      • DRD3
      • 蛋白名称:
      • D(3) dopamine receptor
      • Human Gene Id:
      • 1814
      • Human Swiss Prot No:
      • P35462
      • Mouse Swiss Prot No:
      • P30728
      • 免疫原:
      • Synthesized peptide derived from D3DR . at AA range: 181-230
      • 特异性:
      • D3DR Polyclonal Antibody detects endogenous levels of D3DR 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. ELISA: 1:20000. Not yet tested in other applications.
      • 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:
      • DRD3;D(3) dopamine receptor;Dopamine D3 receptor
      • 实测条带:
      • 44kD
      • 背景:
      • This gene encodes the D3 subtype of the five (D1-D5) dopamine receptors. The activity of the D3 subtype receptor is mediated by G proteins which inhibit adenylyl cyclase. This receptor is localized to the limbic areas of the brain, which are associated with cognitive, emotional, and endocrine functions. Genetic variation in this gene may be associated with susceptibility to hereditary essential tremor 1. Alternative splicing of this gene results in transcript variants encoding different isoforms, although some variants may be subject to nonsense-mediated decay (NMD). [provided by RefSeq, Jul 2008],
      • 功能:
      • disease:Genetic variation in DRD3 may be associated with susceptibility to hereditary essential tremor 1 (ETM1) [MIM:190300]. ETM1 is the most common movement disorder. The main feature is postural tremor of the arms. Head, legs, trunk, voice, jaw, and facial muscles also may be involved. The condition can be aggravated by emotions, hunger, fatigue and temperature extremes, and may cause a functional disability or even incapacitation. Inheritance is autosomal dominant.,function:This is one of the five types (D1 to D5) of receptors for dopamine. The activity of this receptor is mediated by G proteins which inhibit adenylyl cyclase.,online information:The Singapore human mutation and polymorphism database,similarity:Belongs to the G-protein coupled receptor 1 family.,subunit:Interacts with CLIC6.,tissue specificity:Brain.,
      • 细胞定位:
      • Cell membrane ; Multi-pass membrane protein . Both membrane-bound and scattered in the cytoplasm during basal conditions. Receptor stimulation results in the rapid internalization and sequestration of the receptors at the perinuclear area (5 and 15 minutes), followed by the dispersal of the receptors to the membrane (30 minutes). DRD3 and GRK4 co-localize in lipid rafts of renal proximal tubule cells.
      • 组织表达:
      • Brain.

      Dysregulation of striatal dopamine D2/D3 receptor-mediated by hypocretin induces depressive behaviors in rats JOURNAL OF AFFECTIVE DISORDERS Kangyu Jin WB Rat striatum
      货号:YT5448

      • 产品图片
      • Western Blot analysis of HeLa cells using D3DR Polyclonal Antibody. Secondary antibody(catalog#:RS0002) was diluted at 1:20000