NPSR1 Antibody, FITC conjugated

說明書

中文名稱：

NPSR1兔多克隆抗體, FITC偶聯(lián)
貨號(hào)：

CSB-PA757818LC01HU
規(guī)格：

￥880
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

產(chǎn)品名稱：

Rabbit anti-Homo sapiens (Human) NPSR1 Polyclonal antibody
Uniprot No.：

Q6W5P4
基因名：

NPSR1
別名：

NPSR1; GPR154; GPRA; PGR14; Neuropeptide S receptor; G-protein coupled receptor 154; G-protein coupled receptor PGR14; G-protein coupled receptor for asthma susceptibility
宿主：

Rabbit
反應(yīng)種屬：

Human
免疫原：

Recombinant Human Neuropeptide S receptor protein (1-52AA)
免疫原種屬：

Homo sapiens (Human)
標(biāo)記方式：

FITC
克隆類型：

Polyclonal
抗體亞型：

IgG
純化方式：

>95%, Protein G purified
濃度：

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

Preservative: 0.03% Proclin 300
Constituents: 50% Glycerol, 0.01M PBS, pH 7.4
產(chǎn)品提供形式：

Liquid
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：

G-protein coupled receptor for neuropeptide S (NPS). Promotes mobilization of intracellular Ca(2+) stores. Inhibits cell growth in response to NPS binding. Involved in pathogenesis of asthma and other IgE-mediated diseases.
基因功能參考文獻(xiàn)：
1. A decreased risk of psychological stress was only found in TT of NPSR1 (rs324981): A allele carriers vs. TT genotype (OR 1.64, 95% CI 1.11, 2.42), and AT genotype vs. TT genotype (OR 1.76, 95% CI 1.17, 2.65). We found that the NPSR1 (rs324981) T/T genotype decreased the risk of psychological stress, while the overall coping style was a risk factor for psychological stress. PMID: 30242809
2. Results show higher fronto-limbic connectivity in adolescent A allele carriers vs. children carrying the A allele, a pattern which could not be discerned in TT homozygotes. Adolescent NPSR1 TT risk genotype carriers vs. adolescent A allele carriers displayed a reduced fronto-amygdala and fronto-insula effective connectivity suggesting basis of risk-increasing effect of the NPSR1T allele for anxiety. PMID: 26503268
3. Sequence variation in NPSR1 may contribute to sex differences in stress regulation. PMID: 27883964
4. we have utilized a broad-scaled affinity proteomics approach to identify three proteins (CCL5, HPGDS, and NPSR1) with altered plasma levels in asthmatic children compared to healthy controls, representing the first evaluation of HPGDS and NPSR1 in plasma. PMID: 27145233
5. The interaction between 5-HTT (LL) and BDNF (A+) increased the risk of anxiety, and the interaction between BDNF (A+, GG) and NPSR1 (AA, T+) increased the risk of depression in asthmatic patients. PMID: 27176146
6. findings demonstrate that hNPS-(1-10) is a biased agonist favoring Galphaq-dependent signaling. It may represent a valuable chemical probe for further investigation of the therapeutic potential of human NPS receptor-directed signalingin vivo. PMID: 26865629
7. anxiety sensitivity correlated negatively with prefrontal activity in NPSR1 rs324981 carriers possibly suggesting a decompensation of the adaptive compensatory upregulation PMID: 25971599
8. Results suggest the functional NPSR1 gene A/T variant to influence glutamate+glutamine concentrations in the bilateral anterior cingulate cortex in healthy male subjects during CCK-4 induced panic PMID: 26235955
9. The T-allele of the NPSR1 rs324981 polymorphism is associated with increased impulsivity and ADHD-related traits in non-clinical cohorts. PMID: 25744621
10. The results suggest neuropeptide S receptor gene variation to be associated with alterations of prefrontal functioning in the attentional functions alerting and executive control partly modulated by anxiety sensitivity. PMID: 25842293
11. Results show that NPSR1 polymorphism is associated with AUD and alcohol consumption, dependent on sex, environment and age. PMID: 24754478
12. gene polymorphism is a risk factor for high IgE-associated atopic eczema at the age of two years in Finland if there is no probiotic treatment PMID: 24439655
13. The functional SNP rs324981 located in the gene of NPSR1 was significantly associated with objectively obtained sleep parameters in a sample of elderly white subjects PMID: 24896296
14. results suggest a potential protective function of the NPSR1 rs324981 A/A genotype against pathologically enhanced anxiety that might be explained by stronger reflective prefrontal regulation over the subcortical fear response. PMID: 23103692
15. Genetic variation at the NPSR1 locus impacts children's predisposition to ecurrent abdominal pain episodes in a Swedish population. PMID: 25091462
16. study provides first evidence for the assumption that a NPSR1 variant modulates brain activation under stress, interacting with the environmental risk factor urban upbringing PMID: 24800784
17. In the Estonian population, NPSR1 A/T polymorphism together with environmental factors is associated with anxious, depressive and activity-related traits, increased prevalence of affective/anxiety disorders and a higher likelihood of suicidal behaviour. PMID: 24331455
18. NPSR1 A/T polymorphism is associated with impulsivity, ADHD symptoms and personality, mirroring the activity- and anxiety-mediating role of NPSR1. PMID: 23325374
19. Neuropeptide S receptor 1 (NPSR1) activates cancer-related pathways and is widely expressed in neuroendocrine tumors. PMID: 24915894
20. Differential gene-environment effects of the NPSR rs324981 T allele indicate recent life events with respect to anxiety sensitivity. PMID: 22404660
21. NPS receptor may have a pathological role in individuals with severe asthma and/or elevated serum IgE levels. PMID: 24239856
22. The present data demonstrated that QA1 and PI1 act as potent NPSR antagonists in vitro, however their usefulness for in vivo investigations in mice seems limited probably by pharmacokinetic reasons. PMID: 23911665
23. Relate NPSR1 genotype to early onset obsessive-compulsive disorder. PMID: 23680103
24. The results of this study showed involvement of the NPS system in the regulation of the neuroendocrine stress response in humans. PMID: 23466585
25. RORA SNPs are associated with childhood asthma and show epistasis with NPSR1, and the interaction between RORA and NPSR1 may be of biological relevance. PMID: 23565190
26. In summary, the more active NPSR1 T allele may confer enhanced response inhibition and increased error monitoring and might drive particularly error monitoring as a neurophysiological endophenotype of anxiety PMID: 23319044
27. NPS is able to stimulate human monocyte chemotaxis and that this effect is entirely due to selective NPSR activation. PMID: 23142110
28. DNA methylation levels in the promoter of NPSR1 showed small but significant associations with asthma and to related traits such as allergy and certain environmental exposures. PMID: 23372674
29. we consider NPSR as a promising target for antipsychotic drug development PMID: 22078257
30. analysis of molecular evolution of the neuropeptide S receptor and cross-species comparison PMID: 22479518
31. NPSR1 gene is associated with reduced risk of rheumatoid arthritis. PMID: 22548958
32. findings represent a first step to decipher NPSR1 locus complexity and its impact on several human conditions NPS antagonists have been recently described, and our results are of potential pharmacogenetic relevance PMID: 22216302
33. Ther neuropeptide S receptor genotype is associated with increased amygdala responsiveness to fear-relevant stimuli. PMID: 21525857
34. results provide converging evidence for a female-dominant role of NPSR gene variation in panic disorder through heightened autonomic arousal and distorted processing of anxiety-relevant emotional stimuli. PMID: 20603625
35. There is an NPSR1 isoform-specific link to pathogenetic processes in asthma and allergy. PMID: 21707994
36. data suggest a genetic and neuroanatomical substrate for catastrophizing overinterpretations of fear reactions. PMID: 20628342
37. The available information regarding NPS and its receptor and the biological actions modulated by the NPS-NPSR system, is summarized. PMID: 19824051
38. NPS-NPSR1 signaling is likely involved in anxiety PMID: 20705147
39. Observational study of gene-disease association and gene-environment interaction. (HuGE Navigator) PMID: 20701904
40. Data show that NPSR1 polymorphism may be relevant to RA susceptibility and its clinical manifestation. PMID: 20179762
41. Observational study of gene-disease association. (HuGE Navigator) PMID: 19913121
42. Observational study of gene-disease association. (HuGE Navigator) PMID: 20603625
43. Observational study of gene-disease association, gene-environment interaction, and pharmacogenomic / toxicogenomic. (HuGE Navigator) PMID: 20628086
44. Observational study of gene-disease association. (HuGE Navigator) PMID: 20628342
45. Observational study of gene-disease association. (HuGE Navigator) PMID: 20705147
46. Clinical trial of gene-disease association and gene-environment interaction. (HuGE Navigator) PMID: 20379614
47. Observational study of gene-disease association. (HuGE Navigator) PMID: 20503287
48. Results suggest that N-linked glycosylation is not important for neuropeptide S receptor biogenesis or function, and that residue D105 might be critical for receptor binding. PMID: 19874863
49. Observational study of gene-disease association. (HuGE Navigator) PMID: 20179762
50. Expression of several neuropeptides is induced upon NPS-NPSR1 signaling; NPSR1 variants are associated with colonic transit in functional gastrointestinal diseases PMID: 19732772
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相關(guān)疾病：

Asthma-related traits 2 (ASRT2)
亞細(xì)胞定位：

[Isoform 1]: Cell membrane; Multi-pass membrane protein.; [Isoform 3]: Cell membrane; Multi-pass membrane protein.; [Isoform 4]: Cell membrane; Multi-pass membrane protein.; [Isoform 2]: Cytoplasm.; [Isoform 5]: Cytoplasm.; [Isoform 6]: Cytoplasm.; [Isoform 7]: Cytoplasm.; [Isoform 9]: Cytoplasm.
蛋白家族：

G-protein coupled receptor 1 family, Vasopressin/oxytocin receptor subfamily
組織特異性：

Isoform 4 is ubiquitous; it is detected in glandular epithelia of bronchus, stomach, small intestine, colon, uterus, esophagus, spleen, kidney, pancreas, prostate and breast. Isoform 1 is detected in uterus, colon and prostate, and in the smooth muscle ce
數(shù)據(jù)庫鏈接：

HGNC: 23631

OMIM: 608584

KEGG: hsa:387129

STRING: 9606.ENSP00000352839

UniGene: Hs.652373

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