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D3DR Polyclonal Antibody
商品货号: PLA019114
适 应 性: 人,小鼠,大鼠
WB ELISA
¥600元
规格:
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MSDS
说明书
商品描述
  • 基因名称: DRD3
  • 蛋白名称: D(3) dopamine receptor
  • Human_gene_id: 1814
  • Human_gene_link: http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=1814
  • Human_swiss_prot_no: P35462
  • Human_swiss_link: http://www.uniprot.org/uniprotkb/P35462/entry
  • Mouse_gene_id: 13490
  • Mouse_gene_link: http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=13490
  • Mouse_swiss_prot_no: P30728
  • Mouse_swiss_link: http://www.uniprot.org/uniprot/P30728
  • Rat_gene_id: 29238
  • Rat_gene_link: http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=29238
  • Rat_swiss_prot_no: P19020
  • Rat_swiss_link: http://www.uniprot.org/uniprot/P19020
  • 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)
  • 说明书: 1
  • Msds: MSDS_Antibody.pdf
  • 其他名称: DRD3; D(3) dopamine receptor; Dopamine D3 receptor
  • 实测条带: 44kD
  • 信号通路: Neuroactive ligand-receptor interaction;
  • 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.,
  • 相关产品: RS0001,RS0002,YM3028,YM3029
  • 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.
  • 科研货号: PLA019114
D3DR Polyclonal Antibody
Catalog No PLA019114
Product information
  • 基因名称: DRD3
  • 蛋白名称: D(3) dopamine receptor
  • Human_gene_id: 1814
  • Human_gene_link: http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=1814
  • Human_swiss_prot_no: P35462
  • Human_swiss_link: http://www.uniprot.org/uniprotkb/P35462/entry
  • Mouse_gene_id: 13490
  • Mouse_gene_link: http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=13490
  • Mouse_swiss_prot_no: P30728
  • Mouse_swiss_link: http://www.uniprot.org/uniprot/P30728
  • Rat_gene_id: 29238
  • Rat_gene_link: http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=29238
  • Rat_swiss_prot_no: P19020
  • Rat_swiss_link: http://www.uniprot.org/uniprot/P19020
  • 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)
  • 说明书: 1
  • Msds: MSDS_Antibody.pdf
  • 其他名称: DRD3; D(3) dopamine receptor; Dopamine D3 receptor
  • 实测条带: 44kD
  • 信号通路: Neuroactive ligand-receptor interaction;
  • 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.,
  • 相关产品: RS0001,RS0002,YM3028,YM3029
  • 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.
  • 科研货号: PLA019114
  • Hunan UPT Biotechnology Co.,Ltd
    Website:www.uptbio.com Servive hotline :4006916686
    E-mail:service@uptbio.com
    Address:
    Room 402, Building 13, Xinggong International Industrial Park, 100 Guyuan Road, Yuelu District, Changsha City, Hunan Province, China.
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