UCP3 Antibody

說明書

中文名稱：

UCP3兔多克隆抗體
貨號：

CSB-PA004385
規格：

￥1090
圖片：
Western Blot analysis of Jurkat cells using UCP3 Polyclonal Antibody
其他：

產品詳情
產品評價
相關產品
靶點詳情

產品詳情

Uniprot No.：

P55916
基因名：

UCP3
別名：

UCP3; SLC25A9; Mitochondrial uncoupling protein 3; UCP 3; Solute carrier family 25 member 9
宿主：

Rabbit
反應種屬：

Human,Mouse,Rat
免疫原：

Synthesized peptide derived from the C-terminal region of Human UCP3.
免疫原種屬：

Homo sapiens (Human)
標記方式：

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.
產品提供形式：

Liquid
應用范圍：

WB, ELISA

推薦稀釋比：

Application	Recommended Dilution
WB	1:500-1:2000
ELISA	1:10000

Protocols：

Western Blotting (WB) Protocol
ELISA 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：

UCP are mitochondrial transporter proteins that create proton leaks across the inner mitochondrial membrane, thus uncoupling oxidative phosphorylation. As a result, energy is dissipated in the form of heat. May play a role in the modulation of tissue respiratory control. Participates in thermogenesis and energy balance.
基因功能參考文獻：
1. findings indicate that polymorphisms rs3813929 and rs1800849 from 5-HT2C and UCP3 genes were related to type 2 diabetes mellitus prevalence among the Brazilian obese women candidates for bariatric surgery. PMID: 28977211
2. In type 2 diabetics the combination of UCP3-55 CC and PPARgamma2 Pro12Ala genotypes is associated with significantly higher BMI than other PPARgamma2-UCP3 genotype combinations, partly due to a reduced ability in lipids oxidation. PMID: 27089973
3. genetic association studies in population in Spain: Data suggest that responses among obese patients (weight loss and changes in insulin resistance/cardiovascular risk factors) to high protein/low carbohydrate reducing diet varies according to a genetic polymorphism in the promoter region of UCP3 (-55CT, rs1800849). PMID: 26848765
4. Combined, our data suggest functional significance of UCP-3 for H/R resistance PMID: 26304588
5. UCP3 overexpression limits keratinocyte proliferation and tumorigenesis through inhibition of Akt. PMID: 26310111
6. Children with UCP-3 -55 T/T genotype had a significantly lower adjusted metabolic rate than the C allele carriers. PMID: 25081806
7. A newly identified functional variant (rs1626521) in UCP-3 affects postprandial gastric functions and satiety and may contribute to weight gain and alter human mitochondrial function PMID: 25755013
8. UCP3 genotype prevailed in the women of besieged Leningrad compared to relevant control groups of the persons of the same age who did not suffered hungry disaster. PMID: 25826986
9. Studied the impact of SNPs in/near UCP3 and RPTOR on obesity-related traits. PMID: 25533680
10. The study replicates in two independent populations the association between the -55CT polymorphism of UCP3 and a lower BMI. PMID: 24026107
11. In patients with -55CC UCP3 genotype, a high mono-unsaturated hypocaloric diet reduced BMI, weight, waist circumference, waist to hip ratio, fat mass, LDL-cholesterol, total cholesterol and leptin levels. PMID: 24174365
12. A higher prevalence of UCP3 rs11235972 GG genotype was observed in Chinese children with nonalcoholic fatty liver disease. PMID: 24124336
13. T allele of the UCP3 gene was favourable in obtaining higher VOmax (maximum oxygen uptake)level and might be considered as endurance-related allele PMID: 23505621
14. The T allele carriers of -55CT UCP3 polymorphism exhibit no metabolic response to weight loss induced by a hypocaloric diet rich in polyunsaturated fatty acids PMID: 23165529
15. No association has been found between UCP3 -55C/T polymorphism and obesity in the populations investigated. (Meta-analysis) PMID: 23560041
16. This study demonistrated that Polymorphisms in uncoupling protein genes UCP3 is not associated with HIV-associated sensory neuropathy in African individuals. PMID: 23521650
17. A significant association has been found between the UCP2 Ala55Val polymorphisms and increased susceptibility for type 2 diabetes mellitus in Asians. PMID: 23365654
18. Results show prevalence of mutant UCP genotypes was similar in patients with metabolic syndrome (75.7% wild genotype and 24.3% mutant genotype) and without MS (69.7% wild genotype and 30.3% mutant genotype). PMID: 22811361
19. genetic association study in population in Spain: Data suggest that a polymorphism in promoter region of UCP3 gene (-55CC->CT) is associated with fat distribution/adiposity and cardiovascular risk factors in obese subjects with type 2 diabetes. PMID: 21897112
20. Report interaction of -55CT polymorphism of UCP3 gene with Trp64Arg polymorphism of beta3adrenoreceptor gene on insulin resistance in obese patients. PMID: 22774401
21. Our results also suggest that telmisartan, which increases fatty acid oxidation in rat skeletal muscle, also improves UCP3 wt and mutant protein activity, including the dominant-negative UCP3 mutants. PMID: 21544083
22. UCP3 -55C/T polymorphism may be risk factor for susceptibility to type 2 diabetes in individuals of Asian descent, but not in individuals of European descent (Meta-Analysis) PMID: 21751002
23. The sensitivity of SERCA to mitochondrial ATP production suggests that mitochondria control the local ATP availability at ER Ca(2+) uptake and release sites. PMID: 21775425
24. conclude that a more efficient uncoupling process has a beneficial effect on the aging muscle by slowing down its age related decay PMID: 21336965
25. The genotype and the allele frequencies of -55C/T of the UCP3 gene showed a significant protective effect against the development of diabetes. PMID: 21175267
26. Results suggest that adaptation to climate influenced the global distribution of allele frequencies in UCP1 and UCP3 and provide an independent source of evidence for a role in cold resistance for UCP3. PMID: 20802238
27. Data demonstrate that distinct sites in the IML2 of UCP3 effect mitochondrial uptake of high and low Ca(2+) signals. PMID: 21047682
28. -55CT genotype is associated with high insulin resistance and low adiponectin levels than -55CC genotype. Patients with -55CT genotype have more frequently moderate-severe steatosis and inflammation than -55CC genotype PMID: 20694293
29. Polymorphism -55C/T of the UCP3 promotor did not have an effect on weight loss or clinical outcomes after bariatric surgery. PMID: 18484143
30. Cardiorespiratory fitness modifies the association between the rs1800849 polymorphism and homocysteine so that the negative effect of the T allele does not persist in youth with moderate to high levels of fitness. PMID: 20031128
31. mutant-type group of -55CC UCP3 gene patients had higher weight, fat mass, and insulin resistance than wild-type group. PMID: 19913848
32. Uncoupling protein 3 gene is associated with body composition changes with training. PMID: 11842047
33. mitochondrial uncoupling protein, involved in thermogenesis. mRNA levels elevated in weight loss associated with gastrointestinal adenocarcioma. PMID: 11875702
34. Fasting activates the gene expression of UCP3 independent of lipid transport and oxidation genes in skeletal muscle suggesting a role in regulation of FA homeostasis during fasting PMID: 12051710
35. UCP3 protein content is related to energy metabolism in humans and might help in the metabolic adaptation to cold exposure PMID: 12075570
36. Depressed UCP3 expression may be an important mechanism for reducing the formation of oxygen-derived free radicals. PMID: 12145475
37. Metabolic and anthropometric factors related to skeletal muscle UCP3 gene expression in healthy human adults. PMID: 12217879
38. expression of UCP3 mRNA was dependent on human muscle differentiation PMID: 12351640
39. role of UCP3 in postnatal activation of lipid oxidation in skeletal muscle and suggest the involvement of UCP3 in the delayed activation of mitochondrial energy conversion in very immature preterm neonates. PMID: 12612210
40. Training status did not change skeletal muscle fiber hierarchical UCP3 protein expression in different fiber types. It affected UCP3 content more in type I and type IIa than in type IIx muscle fibers. PMID: 12634927
41. purine nucleotides must be the physiological inhibitors of UCP3-mediated uncoupling in vivo. PMID: 12670931
42. study of isolation, refolding, transport properties, and regulation of recombinant UCP3 PMID: 12734183
43. Uncoupling protein 3 polymorphisms are associated with waist-to-hip ratio. PMID: 12756473
44. This is the first study to demonstrate a downregulation of skeletal muscle UCP3 mRNA expression after the lowering of plasma free fatty acids concentrations in humans, despite an increase in energy expenditure upon beta2-adrenergic stimulation. PMID: 12824081
45. convergence of MyoD and PPAR-dependent pathways provides a molecular mechanism for skeletal muscle specificity and fatty acid regulation of the human UCP3 gene. PMID: 12843208
46. Up-regulation of UCP3 in riboflavin-responsive, multiple acylcoenzyme A dehydrogenase deficiency is due to accumulation of muscle fatty acid/acylCoA. PMID: 14671191
47. Results support a role for UCP3 in fuel substrate management and energy metabolism, which may influence body weight regulation. PMID: 15045692
48. Association between BMI and the UCP3 -55 C-->T polymorphism in diabetic nephropathy. PMID: 15120704
49. IGF-1 may protect from hyperglycemia-induced oxidative stress and neuronal injuries by regulating mitochondrial membrane potential, possibly by the involvement of UCP3. PMID: 15211595
50. No association was found between the -55 C/T polymorphism within the uncoupling protein 3 gene and the ultra-endurance performance of triathletes. PMID: 15346230
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相關疾病：

Obesity (OBESITY)
亞細胞定位：

Mitochondrion inner membrane; Multi-pass membrane protein.
蛋白家族：

Mitochondrial carrier (TC 2.A.29) family
組織特異性：

Only in skeletal muscle and heart. Is more expressed in glycolytic than in oxidative skeletal muscles.
數據庫鏈接：

HGNC: 12519

OMIM: 601665

KEGG: hsa:7352

STRING: 9606.ENSP00000323740

UniGene: Hs.101337

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