CHRNA5 Antibody

說明書

中文名稱：

CHRNA5兔多克隆抗體
貨號：

CSB-PA005391GA01HU
規格：

￥3,900
其他：

產品詳情
產品評價
相關產品
靶點詳情

產品詳情

Uniprot No.：

P30532
基因名：

CHRNA5
別名：

CHRNA5; NACHRA5; Neuronal acetylcholine receptor subunit alpha-5
宿主：

Rabbit
反應種屬：

Human,Mouse,Rat
免疫原：

Human CHRNA5
免疫原種屬：

Homo sapiens (Human)
抗體亞型：

IgG
純化方式：

Antigen Affinity Purified
濃度：

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

PBS with 0.1% Sodium Azide, 50% Glycerol, pH 7.3. -20°C, Avoid freeze / thaw cycles.
產品提供形式：

Liquid
應用范圍：

ELISA,WB
Protocols：

ELISA Protocol
Western Blotting (WB) Protocol
儲存條件：

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.

產品評價

靶點詳情

功能：

After binding acetylcholine, the AChR responds by an extensive change in conformation that affects all subunits and leads to opening of an ion-conducting channel across the plasma membrane.
基因功能參考文獻：
1. Glutamatergic N398 neurons responded to lower nicotine doses (0.1 muM) with greater frequency and amplitude but they also exhibited rapid desensitization, consistent with previous analyses of N398-associated nicotinic receptor function PMID: 27698409
2. Increased habenula-striatum functional connectivity may be modulated by the nicotinic receptor variant rs16969968 and may lead to increased Opioid use. PMID: 28857330
3. Our present study suggested that rs667282 in CHRNA5-A3 may modify the prognosis of patients with advanced non-small cell lung cancer PMID: 27050379
4. The data replicate previous result suggesting CHRNA5 as a candidate gene for chronic obstructive pulmonary disease (COPD) and rs8040868 as a risk variant for the development of COPD in the Swedish population. PMID: 27835950
5. Polymorphisms in the CHRNA5 and NRXN1 genes, influenced greater consumption of cigarettes in a Mexican Mestizo population. PMID: 27355804
6. RP11-650L12.2 rs149941240 polymorphism was associated with the risk of colorectal cancer. PMID: 28442398
7. We determined that the other patients harbored mutations in genes that have not previously been linked to RTT or other neurodevelopmental syndromes, such as the ankyrin repeat containing protein ANKRD31 or the neuronal acetylcholine receptor subunit alpha-5 (CHRNA5). PMID: 27541642
8. quitting smoking is highly beneficial in reducing lung cancer risks for smokers regardless of their CHRNA5 rs16969968 genetic risk status. Smokers with high-risk CHRNA5 genotypes, on average, can largely eliminate their elevated genetic risk for lung cancer by quitting smoking- cutting their risk of lung cancer in half and delaying its onset by 7years for those who develop it. PMID: 27543155
9. Study showed that multiple rare, low frequency and common variants in the CHRNA5 gene contribute to the development of nicotine dependence PMID: 26239294
10. There was no association of rs16969968 polymorphism at CHRNA5 with cancer risk in the overall pooled analysis PMID: 27072204
11. rs2036527 is a risk factor for smoking exposure and lung cancer association in African-Americans. PMID: 26981579
12. Preventive interventions in adolescents reduced the genetic risk for smoking from rs16969968 CHRNA5. PMID: 25941207
13. suggest that gene variance in the CHRNA5-CHRNA3-CHRNB4 cluster is associated with an increased risk of death, incidence of COPD and tobacco-related cancer in smokers PMID: 26689306
14. These results suggest that exposure to nicotine might negatively impact the apoptotic potential of chemotherapeutic drugs and that alpha5-nAChR/AKT signaling plays a key role in the anti-apoptotic activity of nicotine induced by cisplatin. PMID: 26909550
15. A novel regulatory SNP association with nicotine dependence was found. Previously observed differences in CHRNA5 mRNA expression and nicotine dependence risk were connected to underlying DNA methylation differences. PMID: 26220977
16. Our meta-analysis provided statistical evidence for a strong association between rs16969968 polymorphism and the risk of lung cancer, especially in smokers and Caucasians. PMID: 26434895
17. This study showed that CHRNA5(rs16969968) interacted with chronic low family support in association with child mental health status PMID: 26228411
18. No associations were found between the analyzed variants and smoking, however, there was an association among non-smoking subjects between the A allele of rs16969968 and high body mass index. PMID: 26757861
19. In non-Hispanic White participants, a novel association between rs1289899 in the CHRNA5 gene and posttraumatic stress disorder was observed. PMID: 26184988
20. A low to moderate level of Nicotine Dependence in the Kashubians, of Poland, influenced by age, sex, as well as the CHRNA5 rs16969968 variant was demonstrated PMID: 25652844
21. Results indicate that the minor alleles of both polymorphisms modulate response speed in a sex-dependent, diametrically opposed manner. PMID: 25674902
22. The CHRNA5 genetic risk synergized the effect of partner smoking, producing an especially low likelihood of successful smoking reduction in two complementary studies. PMID: 25073833
23. CHRNA5 rs3841324 combined variant genotypes (ins/del+del/del) had a >1.5-fold elevated risk for nasopharyngeal carcinoma PMID: 25329654
24. Genetic variation in CHRNA5 protein influence smoking behaviors and the level of carbon monoxide. PMID: 25072098
25. CHRNA5 SNPs predicted nicotine deprivation-induced reduction in cognitive control. PMID: 24934182
26. Among smokers who are hospitalized with acute myocardial infarction, the high-risk CHRNA5 allele was associated with lower likelihood of quitting before hospitalization and significantly less abstinence 1 year after hospitalization with MI. PMID: 24727484
27. The effect of nicotine replacement on continuous abstinence is moderated by the combined genetic risks from CYP2A6 and CHRNA5. PMID: 24033696
28. Single nucleotide polymorphism in CHRNA5 is associated with lung cancer. PMID: 25187487
29. Data found that DRD2 rs1076560 and CHNRA5 rs16969968 interact to modulate cognitive function, prefrontal physiology during working memory, and prefrontal gray matter volume. PMID: 24819610
30. in African-Americans, variants (common or rare) in genes other than CHRNA5 most likely contribute toward the nicotine-dependent phenotype. PMID: 24682045
31. substance dependence associated variants have a direct cis-regulatory effect on CHRNA5 transcript levels in human frontal cortices of African and European ancestry. PMID: 24303001
32. Among African Americans, CHRNA5-A3-B4 variants are not associated with smoking but can influence smoking abstinence. PMID: 24733007
33. The present study investigated the association of CHRNA5 polymorphisms and smoking topography. PMID: 23358500
34. the heterozygous genotype c.-166T>A at rs503464 of CHRNA5 may be associated with reduced risk of lung cancer, thus representing a susceptibility allele in Chinese individuals. PMID: 23314339
35. Silencing of alpha5-nAChR significantly inhibits nicotine-induced cell proliferation in tumor cell lines. PMID: 24793809
36. Women with the variant AA genotype of CHRNA5 rs16969968 or variant CC genotype of LOC123688 rs8034191 were at significantly increased risk of heavy smoking. PMID: 21810735
37. the alpha5 subunit can occupy the position of a nonbinding subunit, or replace a beta2 subunit participating in a canonical binding site. PMID: 24184962
38. CHRNA5 polymorphism was associated with pack-year of smoking in chronic obstructive pulmonary disease Chinese Han patients PMID: 22914670
39. Evaluated the association between CHRNA5-A3-B4 gene cluster variants (rs667282 and rs3743073, two variants modifying lung cancer risk) and risk of gastric cancer. PMID: 23576140
40. The rs588765 nicotine dependence risk allele 'C' was associated with delayed age at onset among ever-smokers(even when smoking intensity variables are accounted for), but had no significant effect among never smoked. PMID: 22884254
41. our findings provide evidence for the presence of multiple CHRNA5 mRNA isoforms that may modulate the multimeric nicotine receptor and cis-regulatory variations in the CHRNA5 locus that act in vivo in the control of CHRNA5 mRNA expression PMID: 23430818
42. Single-nucleotide polymorphism in the CHRNA5 gene is associated with lung cancer susceptibility. PMID: 23221128
43. Findings of this study suggest that personality measures may play an important role in substance use disorders on both environmental (marriage) and genetic rs16969968 in CHRNA5 levels. PMID: 23308091
44. Nicotinic acetylcholine receptor single nucleotide polymorphism is associated with response to smoking cessation therapies. PMID: 23249876
45. The intronic rs871058, that is highly correlated with rs16969968 in CHRNA5, while shows a modest treatment effect for subjects who possess the rare allele has a large effect for not carriers. PMID: 23061658
46. results showed that several of the polymorphisms and their haplotypes in CHRNA5/CHRNA3 genes may have functional effects on (i) CHRNA5 mRNA levels, (ii) polycyclic aromatic hydrocarbon-DNA adduct levels, (iii) susceptibility to lung cancer PMID: 23011884
47. alpha3beta4alpha5 nicotinic acetylcholine receptors, expressing the the N398 variant of CHRNA5, exhibits a reduced response to agonists when extracellular calcium is high and it may lead to distinct downstream cellular signaling. PMID: 22820273
48. Two specific aspects of executive functioning related to drug addiction--impulsivity and working memory--are demonstrated in transgenic mice overexpressing alpha3/alpha5/beta4 nicotinic receptor subunits. PMID: 22024278
49. The A allele of the single nucleotide polymorphism rs16969968 (alpha5, G > A), which correlates with the development of lung cancer, shows a non-significant trend to be associated with cervical lesions. PMID: 22406075
50. Results suggest important role for CHRNA5 variants as genetic risk factor for airflow obstruction that may be independent of smoking status. PMID: 22837378
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亞細胞定位：

Cell junction, synapse, postsynaptic cell membrane; Multi-pass membrane protein. Cell membrane; Multi-pass membrane protein.
蛋白家族：

Ligand-gated ion channel (TC 1.A.9) family, Acetylcholine receptor (TC 1.A.9.1) subfamily, Alpha-5/CHRNA5 sub-subfamily
數據庫鏈接：

HGNC: 1959

OMIM: 118505

KEGG: hsa:1138

STRING: 9606.ENSP00000299565

UniGene: Hs.1614

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