Rabbit Dopamine D2 receptor ELISA Kit | D2R elisa kit
Rabbit Dopamine D2 receptor ELISA Kit
NCBI and Uniprot Product Information
NCBI Description
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, Jul 2008]
Uniprot Description
Function: Dopamine receptor whose activity is mediated by G proteins which inhibit adenylyl cyclase
By similarity. Ref.17
Subunit structure: Forms homo- and heterooligomers with DRD4. The interaction with DRD4 may modulate agonist-induced downstream signaling. Interacts with GPRASP1, PPP1R9B and CLIC6
By similarity. Interacts with CADPS and CADPS2. Interacts with ARRB2
By similarity. Interacts with GNAI1. Interacts with GNAI2 isoform sGi2, the interaction allows the creation of an intracellular pool of DRD2 that can be released to cell surface upon agonist stimulation. Ref.14 Ref.15 Ref.16 Ref.17
Subcellular location: Cell membrane; Multi-pass membrane protein.
Polymorphism: Genetic variations in DRD2 may determine the genetic susceptibility to alcoholism [
MIM:103780]. Genetic variations in DRD2 might be a protective factor against the development of withdrawal symptoms but might also be a risk factor in a highly burdened subgroup of alcoholics with a paternal and grandpaternal history of alcoholism and might contribute to suicide risk in alcoholics.
Involvement in disease: Dystonia 11 (DYT11) [MIM:159900]: A myoclonic dystonia. Dystonia is defined by the presence of sustained involuntary muscle contractions, often leading to abnormal postures. DYT11 is 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.Note: The gene represented in this entry may be involved in disease pathogenesis. DRD2 mutations in myoclonic dystonia patients are rare, and their contribution to disease phenotype is unclear (Ref.22). Ref.20 Ref.22
Sequence similarities: Belongs to the G-protein coupled receptor 1 family.
Research Articles on D2R
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Product Notes
The Rabbit D2R drd2 (Catalog #AAA721931) is an ELISA Kit and is intended for research purposes only. The product is available for immediate purchase. The AAA721931 ELISA Kit recognizes Rabbit D2R. It is sometimes possible for the material contained within the vial of "Dopamine D2 receptor, ELISA Kit" to become dispersed throughout the inside of the vial, particularly around the seal of said vial, during shipment and storage. We always suggest centrifuging these vials to consolidate all of the liquid away from the lid and to the bottom of the vial prior to opening. Please be advised that certain products may require dry ice for shipping and that, if this is the case, an additional dry ice fee may also be required.Precautions
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