DRD3 Antibody

說明書

中文名稱：

DRD3兔多克隆抗體
貨號(hào)：

CSB-PA005795
規(guī)格：

￥1090
圖片：
Western Blot analysis of HeLa cells using D3DR Polyclonal Antibody.
其他：

產(chǎn)品詳情
產(chǎn)品評(píng)價(jià)
相關(guān)產(chǎn)品
靶點(diǎn)詳情

產(chǎn)品詳情

Uniprot No.：

P35462
基因名：

DRD3
別名：

DRD3; D(3 dopamine receptor; Dopamine D3 receptor
宿主：

Rabbit
反應(yīng)種屬：

Human,Mouse,Rat
免疫原：

Synthesized peptide derived from the Internal region of Human D3DR.
免疫原種屬：

Homo sapiens (Human)
標(biāo)記方式：

Non-conjugated
抗體亞型：

IgG
純化方式：

The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
濃度：

It differs from different batches. Please contact us to confirm it.
保存緩沖液：

Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
產(chǎn)品提供形式：

Liquid
應(yīng)用范圍：

WB, ELISA

推薦稀釋比：

Application	Recommended Dilution
WB	1:500-1:2000
ELISA	1:20000

Protocols：

Western Blotting (WB) Protocol
ELISA Protocol
儲(chǔ)存條件：

Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
貨期：

Basically, we can dispatch the products out in 1-3 working days after receiving your orders. Delivery time maybe differs from different purchasing way or location, please kindly consult your local distributors for specific delivery time.
用途：

For Research Use Only. Not for use in diagnostic or therapeutic procedures.

產(chǎn)品評(píng)價(jià)

靶點(diǎn)詳情

功能：

Dopamine receptor whose activity is mediated by G proteins which inhibit adenylyl cyclase. Promotes cell proliferation.
基因功能參考文獻(xiàn)：
1. This study showed that the DRD3 is a potential genetic factor in the susceptibility to amphetamine dependence and is associated with onset age of drug use through interaction with novelty seeking in a specific patient group in the Han Chinese population. PMID: 28028606
2. The C allele of DRD3 rs6280 SNP was associated with increased risk of sleep bruxism (p = 0.02). PMID: 28451935
3. Associations between 4 polymorphisms (rs11721264, rs3773678, rs167771, rs324035) and Parkinson's diseasehave been found. PMID: 27240184
4. This study adds to the growing evidence on the association of single- and multiple-risk variants in DRD3, DRD4, and FEV with aggressive behavior in Chinese adolescents. PMID: 28846959
5. SNPs (rs9880168) of the DRD3 were associated with Essential Hypertension in Hani nationality However, none SNPs of DRD1 and DRD3 of best models showed association with Essential Hypertension in Han and Yi nationality. PMID: 28579604
6. Lowering the level of cellular FLNA caused an elevation in RalA activity and resulted in selective interference with the normal intracellular trafficking and signaling of D3R through beta-arrestins. Knockdown of FLNA or coexpression of active RalA prevented D3R from coupling with G protein. PMID: 27188791
7. This study reveled that R D3 are upregulated in peripheral blood mononuclear cells in patient with multiple sclerosis. PMID: 27609280
8. Study performed docking essays using risperidone and the D3 receptor crystallographic data and results suggested two possible distinct orientations for risperidone at the binding pocket; data highlight important hot spots in the DRD3 binding site bringing relevant information for the development of novel/derivative agents with atypical profile. PMID: 27434874
9. Applying an external electric field, at different frequencies, in the logarithmic scale along the z-direction on the dopamine-dopamine receptor D3 complex, at some frequencies has a significant effect on salt bridge interaction and the structural observables, although it does not have any systematic or predictable effect on the dynamical and physical property of the protein. PMID: 27832207
10. The results of this study suggest that genotype in DRD3 Ser9Gly was the main factor determining different doses of DAs and PD patients carrying Gly/Gly genotype require higher doses of pramipexole for effective treatment. PMID: 27817855
11. Clathrin-mediated internalization of dopamine receptor D3 was responsible for lysosomal degradation. PMID: 27240955
12. DRD3 Ser9Gly polymorphism is nominally associated with changes in triglycerides and metabolic syndrome after 12 weeks of standard BDII treatment. PMID: 27310943
13. Regarding the DRD3 Ser9Gly polymorphism, individuals with a greater number of the Gly alleles, which are related to an increased dopamine release in the striatum, were more susceptible to social influence. PMID: 27784028
14. DRD3 gene expression reduction in breast cancer patients after spiritual intervention PMID: 26597879
15. This study showed a lack of association between of DRD3 rs6280 with the risk for essential tremor. PMID: 27456607
16. The combination of MTHFR, DRD3 and MDR1 polymorphisms associated with a slow ATV metabolizer phenotype PMID: 26857559
17. The DRD3 (rs6280) polymorphism influences younger Parkinson disease age of onset in the US Caucasian population. PMID: 26627941
18. A significant positive correlation was found between the DRD3 mRNA level and the score of the excited factor in patients with schizophrenia/schizophreniform disorder. PMID: 26561806
19. Ammonia induced autophagy by MTOR is mediated by DRD3. PMID: 27077655
20. Drd3 palmitoylation acts as a molecular switch for Drd3-biased signaling via a GIPC1-dependent route, which is likely to affect the mode of action of antipsychotic drugs. PMID: 26787837
21. used site-directed mutagenesis to identify key residues involved in D3 receptor signaling function PMID: 26116441
22. Review concludes that striatum abnormalities in autism are associated with repetitive and stereotyped behavior in autism and may be related to DRD3 polymorphisms PMID: 25224105
23. Study found a significant association with disordered gambling and rs167771 (DRD3) and with rs381572 (CAMK2D) in humans PMID: 25266122
24. We did not find evidence of association between the other four SNPs (rs167771 and rs324029 in DRD3, rs8076005 and rs2066713 in SCL6A4) and Type 2 Diabetes Mellitus. PMID: 25927430
25. relationship between DRD3 gene SNPs, striatum and stereotyped behavior in autism spectrum disorder PMID: 25792691
26. An interaction between BDNF and DRD3 may not play a major role in the risk for suicide attempt. PMID: 25264289
27. Results show significant association between a variant downstream of DRD3 and a co-morbid major depressive disorder-nicotine dependence phenotype. PMID: 24927283
28. In people with diffuse Lewy body disease, Dopamine D receptor density was significantly increased in the striatal regions including caudate, putamen and nucleus accumbens. PMID: 23732230
29. Findings provide no evidence for an association between DRD3 gene rs6280 and TS in the Han Chinese population. PMID: 25698199
30. results provide insights into the potential contribution of molecules of cholesterol to the overall organization and potential stability of the D3 receptor and possibly other GPCR quaternary structures PMID: 25931118
31. The DRD3 gene body hypermethylation was significantly associated with risk of schizophrenia. PMID: 25262640
32. the results of this study provide initial evidence that polymorphisms in DRD3, perhaps reflecting a single risk locus, may be associated with lifetime post-traumatic stress disorder diagnosis. PMID: 25158632
33. findings of this study suggest that the Dopamine D3 receptor rs6280 polymorphism is associated with the development of Alcohol Dependence in Koreans. PMID: 24776816
34. DRD3 is possibly a genetic factor in the development of early-onset heroin dependence, but is not associated with specific personality traits. PMID: 24398431
35. [review] In addition to its expression and signaling patterns, alterations in D3 receptor expression patterns following drug exposure suggest an important role for D3 signaling in the development of addiction. PMID: 24484980
36. In contrast to a D2 receptor deficiency, cocaine dependent individuals may have heightened D3 receptor levels which could contribute to addiction-relevant traits. PMID: 23921256
37. Dopamine D3 release is increased in dopamine (DRD)2 receptor-rich striatum and DRD3-rich extra-striatal regions in response to smoking. PMID: 23954846
38. Pharmacological sequestration is correlated with desensitization of the D3 receptor in a Gbetagamma- and beta-arrestin-dependent manner. PMID: 23992580
39. the present meta-analysis does not support the notion that the DRD3 Ser9Gly variant is a genetic risk factor for essential tremor. PMID: 24054403
40. psychiatric phenotypes of the BDNF Met666Val and DRD3 Ser9Gly polymorphisms in bipolar disorder comorbid with anxiety disorder PMID: 24021960
41. This study showed that Eight SNPs were nominally associated with SZ in either case-control or family based analyses (p < 0.05, rs7631540 and rs2046496 in DRD3. PMID: 23932573
42. data demonstrate a crucial role for the dynamic interaction between D3R and USP48 in the regulation of NHE3 expression and function PMID: 24308971
43. Significant associations were found between single nucleotide polymorphisms in the DRD3 gene and the pharmacokinetics of lopinavir/ritonavir during treatment of HIV infection. PMID: 24001122
44. Data suggest that dopamine D3 receptors (DRD3) are associated with cognitive function in both healthy individuals and those with neuropsychiatric disorders characterized by cognition defects; DRD3 antagonists may improve cognitive function. [REVIEW] PMID: 23791072
45. The present study suggests some impact of DRD3 gene variation on ECT response, potentially mediated by alteration of striatal engagement during the processing of emotionally rewarding stimuli. PMID: 22093107
46. Selective inhibition of dopamine D3 brain receptors in smokers alleviates craving in smokers after overnight abstinence. PMID: 22968817
47. Cortical dopamine D2/3 receptor function is more involved in some cognitive functions in patients with schizophrenia compared to controls. PMID: 22338593
48. The rs6280 single nucleotide polymorphism is not related to risk for restless legs syndrome. PMID: 23312624
49. This study provided information regarding the influence of Ser9Gly Polymorphism of the D3 Receptor on long-term forgetting of episodic information. PMID: 23363412
50. Allelic association between schizophrenia and the DRD3 rs6280 polymorphism was found, but it did not survive correction for multiple testing. PMID: 22940547
顯示更多

收起更多
相關(guān)疾?。?/div>
Tremor, hereditary essential 1 (ETM1); Schizophrenia (SCZD)
亞細(xì)胞定位：

Cell membrane; Multi-pass membrane protein. Note=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.
蛋白家族：

G-protein coupled receptor 1 family
組織特異性：

Brain.
數(shù)據(jù)庫鏈接：

HGNC: 3024

OMIM: 126451

KEGG: hsa:1814

STRING: 9606.ENSP00000373169

UniGene: Hs.121478

Most popular with customers

YWHAG Recombinant Monoclonal Antibody

Applications: ELISA, WB, IHC

Species Reactivity: Human
YWHAB Recombinant Monoclonal Antibody

Applications: ELISA, WB, IHC, IF, FC

Species Reactivity: Human, Mouse, Rat
Phospho-YAP1 (S127) Recombinant Monoclonal Antibody

Applications: ELISA, WB, IHC

Species Reactivity: Human
XRCC5 Recombinant Monoclonal Antibody

Applications: ELISA, WB, IHC, IF

Species Reactivity: Human
XDH Recombinant Monoclonal Antibody

Applications: ELISA, WB, IHC

Species Reactivity: Human
WT1 Recombinant Monoclonal Antibody

Applications: ELISA, WB, IHC

Species Reactivity: Human
WFDC2 Recombinant Monoclonal Antibody

Applications: ELISA, WB, FC

Species Reactivity: Human
VIM Recombinant Monoclonal Antibody

Applications: ELISA, IHC, IF

Species Reactivity: Human