Merck Millipore代理MABN53 Anti-Dopamine D2 receptor (DRD2) Antibody, clone 2B9;抗-多巴胺D2受体(DRD2)抗体,克隆2B9store at +2℃ to +8℃

2025-06-27

货号:MABN53

品牌:Merck Millipore

规格:200Ug

目录价:¥5359.00

市场价格:¥4555.15

会员价格:¥4287.20

金山科研平台,产品价格货期咨询微信:jinshanbio Description: Anti-Dopamine D2 receptor (DRD2) Antibody, clone 3D9 | MABN53 View All» Promotional Text: Special Shipping Offer on Antibodies100% Performance Guaranteed View All» Molecular Weight: ~50 kDa observed View All» Immunogen: Linear peptide corresponding to human Dopamine D2 receptor. View All» Clone: 3D9 View All» Isotype: IgMκ View All» Background Information: Problems in the CNS dopaminergic system are thought to be the root cause of some neuropsychiatric disorders. Dopamine D2 receptor 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. Dopamine D2 receptor signaling using Nurr1 and ERK may play an important role in mesencephalic dopaminergic neuronal development. Faulty D2 receptors have been common in cases of ROS-dependent hypertension. In addition, defects in DRD2 are associted with alcohol-responsive dystonia, varying susceptability to familial alcoholism as well as a contributing factor to the suicide risk in alcoholics. View All» Species Reactivity:

  • Rat

  • Human

    View All» Species Reactivity Note: Demonstrated to react with rat. Predicted to react with human based on immunogen design. View All» Application Notes: Immunocytochemistry Analysis: A previous lot was used by an independent laboratory to detect Dopamine D2 receptor in Ntera-2 cells and in rat brain neurons. Courtesy of Glenn Morris, Wolfson Centre for Inherited Neuromuscular Disease. View All» Control: Rat spinal cord tissue lysate View All» Quality Assurance: Evaluated by Western Blot in rat spinal cord tissue lysate.Western Blot Analysis: 5 µg/mL of this antibody detected Dopamine D2 receptor on 10 µg of rat spinal cord tissue lysate. View All» Purification Method: CHT Ion exchange View All» Presentation: Purified mouse monoclonal IgMκ in buffer containing 0.1 M Tris-Glycine (pH 7.4), 150 mM NaCl with 0.05% sodium azide. View All» Storage Conditions: Stable for 1 year at 2-8°C from date of receipt. View All» UniProt Number: P14416 View All» Entrez Gene Number: NP_000786 View All» Gene Symbol:
    • DRD2

    • D2DR

    • D2R

      View All» Alternate Names: Dopamine D2 receptor View All» Usage Statement: Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals. View All» Key Applications:
      • Western Blotting

      • Immunocytochemistry

        View All» Entrez Gene Summary: This gene encodes the D2 subtype of the dopamine receptor. This G-protein coupled receptor inhibits adenylyl cyclase activity. A missense mutation in this gene causes myoclonus dystonia; other mutations have been associated with schizophrenia. Alternative splicing of this gene results in two transcript variants encoding different isoforms. A third variant has been described, but it has not been determined whether this form is normal or due to aberrant splicing. [provided by RefSeq]. View All» UniProt Summary: 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.SIZE: 443 amino acids; 50619 Da SUBUNIT: Interacts with GPRASP1, neurabin-2 and CLIC6 (By similarity). Interacts with CADPS and CADPS2.SUBCELLULAR LOCATION: Cell membrane; Multi-pass membrane protein.DISEASE: It has been suggested that DRD2 is involved in psychiatric disorders; especially in schizophrenia. & Defects in DRD2 are associated with myoclonus dystonia (MD) [MIM:159900]; also known as myoclonic dystonia, alcohol- responsive dystonia and dystonia-11 (DYT11). MD is a movement disorder characterized by involuntary lightning jerks and dystonic movements and postures alleviated by alcohol. Inheritance is autosomal dominant. The age of onset, pattern of body involvement, presence of myoclonus and response to alcohol are all variable.SIMILARITY: Belongs to the G-protein coupled receptor 1 family. View All» Product Name: Anti-Dopamine D2 receptor (DRD2), clone 3D9 View All» Concentration: 1 mg/mL View All» Antibody Type: Monoclonal Antibody View All» Qty/Pk: 200 μg View All» Format: Purified View All» Host: Mouse View All»

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