Dopamine Receptor D3/DRD3 Rabbit Monoclonal Antibody

Dopamine Receptor D3/DRD3 Rabbit Monoclonal Antibody

Cat: AMRe87159
Boyut:50μL Fiyat:$168_x000D_
Boyut:100μL Fiyat:$300_x000D_
Uygulama:WB
Reaktivite:Human,Mouse,Rat
Konjuge:Unconjugated
İsteğe bağlı konjugeler: Biotin, FITC (ücretsiz). Diğer 26 konjugatı görün.

Gen Adı:Dopamine Receptor D3/DRD3
Category: 組換えモノクローナル抗体 Tags: , , , , , ,
Dopamine Receptor D3/DRD3 Rabbit Monoclonal Antibody
Konjugasyon: Unconjugated
Recombinant rabbit monoclonal antibody
Uygulama
IHC  ICC/IF  ELISA WB
Reaktivite
Human,Mouse,Rat
Gen Adı
Dopamine Receptor D3/DRD3
Saklama
Aliquot and store at -20°C (valid for 12 months). Avoid freeze/thaw cycles.
Özet
Ürün Adı Dopamine Receptor D3/DRD3 Rabbit Monoclonal Antibody
Açıklama Recombinant rabbit monoclonal antibody
Konak Rabbit
Reaktivite Human,Mouse,Rat
Konjugasyon Unconjugated
Modifikasyon Unmodified
İzotip IgG
Klonalite Monoclonal
Form Liquid
Konsantrasyon Unconjugated
Saklama Aliquot and store at -20°C (valid for 12 months). Avoid freeze/thaw cycles.
Nakliye Ice bags.
Tampon Supplied in 50mM Tris-Glycine(pH 7.4), 0.15M NaCl, 40% Glycerol, 0.01% sodium azide and 0.05% protective protein. Stable for 12 months from date of receipt.
Saflaştırma Affinity Purification
Antijen Bilgisi
Gen Adı Dopamine Receptor D3/DRD3
Alternatif İsimler D3DR; ETM1; FET1
Gen Kimliği 1814
SwissProt Kimliği P35462
İmmünojen A synthetic peptide of human Dopamine Receptor D3/DRD3
Uygulama
Uygulama WB
Seyreltme Oranı WB 1:1000-1:5000
Moleküler Ağırlık Calculated MW:44 kDa; Observed MW:44 kDa
Araştırma Alanı
Arka Plan
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]
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