GNB3 Antibody
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货号:CSB-PA009606GA01HU
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规格:¥3,900
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其他:
产品详情
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Uniprot No.:P16520
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基因名:
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别名:G protein beta 3 subunit antibody; GBB3_HUMAN antibody; GNB3 antibody; GNB3 guanine nucleotide binding protein (G protein), beta polypeptide 3 antibody; GTP binding regulatory protein beta 3 chain antibody; Guanine nucleotide binding protein (G protein) beta polypeptide 3 antibody; Guanine nucleotide binding protein G antibody; Guanine nucleotide binding protein G(I)/G(S)/G(T) beta subunit 3 antibody; Guanine nucleotide-binding protein G(I)/G(S)/G(T) subunit beta-3 antibody; Hypertension associated protein antibody; IG antibody; SG antibody; Transducin beta chain 3 antibody; Tsubunit beta 3 antibody
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宿主:Rabbit
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反应种属:Human,Mouse,Rat
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免疫原:Human GNB3
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免疫原种属:Homo sapiens (Human)
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抗体亚型:IgG
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纯化方式:Antigen Affinity purified
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浓度:It differs from different batches. Please contact us to confirm it.
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保存缓冲液:PBS with 0.1% Sodium Azide, 50% Glycerol, pH 7.3. -20°C, Avoid freeze / thaw cycles.
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产品提供形式:Liquid
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应用范围:ELISA,WB,IHC
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Protocols:
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储存条件:Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
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货期: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.
相关产品
靶点详情
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功能:Guanine nucleotide-binding proteins (G proteins) are involved as a modulator or transducer in various transmembrane signaling systems. The beta and gamma chains are required for the GTPase activity, for replacement of GDP by GTP, and for G protein-effector interaction.
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基因功能参考文献:
- Significant genetic differences of GNB3 rs5443 exist between Southeastern European Caucasians and other populations. Cluster headache pathophysiology and pharmacotherapy response may be affected by GNB3 polymorphisms. PMID: 29959630
- The polymorphism of FTO gene rs17817449 and GNB3 gene rs5443 (C825T) may be a genetic determinant of obesity in Saudi population whereas impact of MC4R Asn274Ser change could not be detected. PMID: 29937877
- the GNB3 C825T polymorphism may contribute to increased risk of cancer, especially of thyroid carcinoma (meta-analysis). PMID: 25536621
- Guanine nucleotide-binding protein (GNB3) C825T polymorphism is not associated with type 2 diabetes mellitus (T2DM). PMID: 28602143
- Meta-analysis: GNB3 C825T polymorphism is related to increased essential hypertension exclusively in Caucasians. PMID: 28540932
- Our study indicates that variations in OXTR and Gbeta3 genes are specifically associated with presence and severity of Separation Anxiety in childhood and adulthood, but not with depression or anxiety in general. PMID: 28499211
- Our results demonstrate the potential use of a GNB3-specific antisense morpholino, as a pharmacogenetic therapy for essential hypertension PMID: 27028457
- No relationship was found between the studied polymorphisms (14094 ACE gene, rs1800469 gene TGFbeta1, GNB3 gene rs5443, rs5186 AGTR1 gene) and the occurrence of primary vesicoureteral reflux. TT genotype polymorphism rs5443 of the GNB3 gene may be a protective factor for improved renal function in patients with primary vesicoureteral reflux. PMID: 27988909
- Interactions between GNB3, CREB1 and negative life events were revealed. Further evidence is provided about the role of the environment in genetic vulnerability to major depression. PMID: 28225778
- Bipolar patients with the TT genotype had a lower BMI, smaller waist circumference, and lower levels of lipids and leptin than those with the CT or CC genotypes undergoing the valproic acid treatment course. PMID: 26856249
- Expressed in cone photoreceptors and ON-bipolar cells, Gbeta3 is essential in phototransduction and ON-bipolar cell signaling. PMID: 27281386
- Mutational analysis of GNB3 in a cohort of 58 subjects with CSNB identified a sporadic case individual with a homozygous GNB3 mutation PMID: 27063057
- The GNB3 TT genotype is a risk factor for coronary artery disease independent of other established cardiovascular risk factors in Chinese hypertensive patients. PMID: 28067546
- The combined effects of ACE and GNB3 polymorphisms showed that no pulmonary hypertension patients with the ACE/GNB3 II/TT genotype exhibited clinical worsening. PMID: 26821322
- Although not statistically significant, women who carried the GNB3 T risk allele gained 6 pounds more than noncarriers, and mean 6-month postpartum BMI differed by 2.2 kg/m(2) between homozygous women PMID: 25510251
- TT genotype of GNbeta3 C825T is more common among patients with functional dyspepsia than among healthy controls. PMID: 26551933
- GNB3 C825T polymorphisms may be correlated with the efficacy of antidepressants in the treatment of MDD, especially among Asians patients. PMID: 25451402
- GNB3 TT genotype was associated with lower left ventricular ejection fraction at 6 and 12 months in women with peripartum cardiomyopathy. PMID: 26915373
- no significant difference in the distribution of genotypes between vasovagal syncope patients and control group PMID: 26925743
- The present review illustrates that the C825T polymorphism is associated with increased cardiovascular risk of death and disease in Caucasian patients, independently of other established cardiovascular risk factors. PMID: 25903425
- The T-allele of GNbeta3 C825Tcan increase susceptibility to depression. After stratification by ethnicity, the same association was found in the Asian subpopulation, but not the Caucasian subpopulation. PMID: 26147511
- our study showed association of C825T polymorphism of the GNB3 with obesity, but did not prove the association this with the degree of obesity i patients with AH. PMID: 26177133
- The GNB3 825T polymorphism is significantly associated with greater visceral fat and higher serum levels in Korean obese women. PMID: 25280441
- GNB3-C825T polymorphism is associated with risk of essential hypertension in the overall population, the Caucasians and the Chinese. PMID: 24346074
- Results show The GNB3 TT genotype was associated with greater therapeutic effect. PMID: 25306451
- TNF-alpha-308G/A and the GNB3 C825T polymorphisms are associated with obesity and Acute Myocardial infarction in the Taiwanese population. PMID: 22408428
- GNB3 825 TT genotype is a significant and independent risk factor for hard coronary events independent of other established cardiovascular risk factors at a population level in male PMID: 25463071
- No statistically significant differences in GNb3 allele frequencies were observed between oesophageal adenocarcinoma cases and controls PMID: 25659220
- this study does not show an association of GNB3 C825T polymorphism with IBS risk [meta-analysis] PMID: 24876757
- In elderly Chinese patients, the GNb3-C825T SNP is not associated with irritable bowel syndrome pathogenesis. PMID: 25037115
- mtDNA 5178A/C and 10398A/G, GNB3 C825T, and eNOS polymorphisms are useful as a genetic basis for longevity. PMID: 24376503
- a polymorphism in guanine nucleotide binding protein beta 3 (GNbeta3) was associated significantly with global sleep quality PMID: 24635757
- the cumulative evidence does not support the proposal that the haplotypes formed by common polymorphisms in the GNB3 might exert influence on representative cardiovascular factors/phenotypes. PMID: 24477587
- The results show that polymorphism in this gene does not predict long term prognosis in functional dyspepsia in Koreans PMID: 24827623
- This study failed to demonstrate a correlation between specific GNB3 SNPs, blood pressure and insulin resistance in hypertension, prehypertension and control groups. PMID: 24722130
- These results provide novel evidence suggesting genetic variation in the 5-prime region of GNB3 moderates depressive symptom trajectories among primary care attendees. PMID: 24882179
- The GNB3 C825T polymorphism influences the efficacy of sildenafil in patients with pulmonary hypertension. The time to clinical worsening was significantly longer in the TT genotype patients than in the CC/CT genotype patients. PMID: 24531084
- GNbeta3 variant C825T associates with functional dyspepsia under an additive model PMID: 24557575
- The presence of GNB3 825T-allele may impair athletic performance and may serve as a genetic marker of low capacity for athletic performance in male basketball players. PMID: 24901079
- C825T GNB3 gene polymorphism was found to be a significant risk factor for the incidence of cardiovascular disease independently of hypertension and other established CVD risk factors in a Japanese population. PMID: 23595158
- findings show C825T GNB3 polymorphism affects the duration and severity of postocclusive reactive hyperemia during the first and third trimesters of pregnancy PMID: 23667878
- Genetic association between the GNB3 C825T polymorphism and hypertension or stroke. [Meta-analysis] PMID: 23799054
- Interactions between genetic variants of FTO and GNB3 influence clinical parameters to augment hypertension PMID: 23691120
- Describe a recurrent copy number variation in a childhood obesity syndrome. This unbalanced chromosome translocation leads to duplication of over 100 genes on chromosome 12, including the obesity candidate gene G protein beta3 (GNB3). PMID: 23980137
- The gene polymorphisms GNB3 C825T might be a risk factor for POTS through the enhanced vagal withdrawal of the heart in children and adolescents. PMID: 22882749
- The GNB3 825T allele was associated with blunted lipolysis in obese females. PMID: 23061407
- The GNB3 polymorphism is an independent risk factor for vasculogenic erectile dysfunction in Iranian males. PMID: 22985949
- I/D polymorphism is a significant independent predictor for variability of plasma ACE activity but the ACE I/D and GNB3 C825T polymorphisms are not significant factors for HTA in the Tunisian population PMID: 23505911
- A splice variant of GTP-binding regulatory protein beta-3 is unstable, and unable to localize properly to the plasma membrane and to activate diverse Gbetagamma effectors including PLCbeta2/3, PI3Kgamma, ERKs and the Rho guanine exchange factor (RhoGEF) PLEKHG2. PMID: 22940628
- genetic variants of the ADD1 and GNB3 genes may have important roles in blood pressure response to the cold pressor test PMID: 22476228
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相关疾病:Night blindness, congenital stationary, 1H (CSNB1H)
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蛋白家族:WD repeat G protein beta family
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数据库链接:
HGNC: 4400
OMIM: 139130
KEGG: hsa:2784
STRING: 9606.ENSP00000229264
UniGene: Hs.631657
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