DRD3 recombinant monoclonal antibody, clone 5B10
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More Files
- More Functions
Western Blot
Western blot analysis of Hela whole cell lysate, U-251 whole cell lysate, U-87 whole cell lysate, K562 whole cell lysate, HL-60 whole cell lysate, Rat Spleen whole cell lysate, Rat Brain whole cell lysate with DRD3 recombinant monoclonal antibody, clone 5B10 (Cat # RAB07447).
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Specification
Product Description
Rabbit recombinant monoclonal antibody raised against human DRD3.
Antibody Species
Rabbit
Immunogen
Original antibody is raised against a synthetic peptide corresponding to human DRD3.
Theoretical MW (kDa)
Calculated MW: 45, 4
Reactivity
Human, Rat
Form
Liquid
Purification
Affinity chromatography purification
Isotype
IgG
Recommend Usage
ELISA
Western Blot (1:500-1:5000)
The optimal working dilution should be determined by the end user.Storage Buffer
In PBS, pH7.4 (150 mM NaCl, 0.02% sodium azide and 50% glycerol)
Storage Instruction
Store at -20°C or -80°C.
Aliquot to avoid repeated freezing and thawing.Note
This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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Applications
Western Blot
Western blot analysis of Hela whole cell lysate, U-251 whole cell lysate, U-87 whole cell lysate, K562 whole cell lysate, HL-60 whole cell lysate, Rat Spleen whole cell lysate, Rat Brain whole cell lysate with DRD3 recombinant monoclonal antibody, clone 5B10 (Cat # RAB07447).Enzyme-linked Immunoabsorbent Assay
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Gene Info — DRD3
Entrez GeneID
1814Protein Accession#
P35462Gene Name
DRD3
Gene Alias
D3DR, ETM1, FET1, MGC149204, MGC149205
Gene Description
dopamine receptor D3
Gene Ontology
HyperlinkGene Summary
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
Other Designations
essential tremor 1
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Interactome
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Pathway
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Disease
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