MC3R Antibody, FITC conjugated

說明書

中文名稱：

MC3R兔多克隆抗體, FITC偶聯
貨號：

CSB-PA013560LC01HU
規格：

￥880
其他：

產品詳情
產品評價
相關產品
靶點詳情

產品詳情

產品名稱：

Rabbit anti-Homo sapiens (Human) MC3R Polyclonal antibody
Uniprot No.：

P41968
基因名：

MC3R
別名：

MC3R; Melanocortin receptor 3; MC3-R
宿主：

Rabbit
反應種屬：

Human
免疫原：

Recombinant Human Melanocortin receptor 3 protein (38-74AA)
免疫原種屬：

Homo sapiens (Human)
標記方式：

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
產品提供形式：

Liquid
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：

Receptor for MSH (alpha, beta and gamma) and ACTH. This receptor is mediated by G proteins which activate adenylate cyclase. Required for expression of anticipatory patterns of activity and wakefulness during periods of limited nutrient availability and for the normal regulation of circadian clock activity in the brain.
基因功能參考文獻：
1. This article reviews the MC3R polymorphisms and mutations identified in humans, and the in vitro, murine, and human cohort studies examining their putative effects. Certain human MC3R mutations are associated with greater adiposity and hyperleptinemia. [review] PMID: 28363697
2. Structural Insights into Selective Ligand-Receptor Interactions Leading to Receptor Inactivation Utilizing Selective Melanocortin 3 Receptor Antagonists. PMID: 28715181
3. MC3R mutations are associated with Obesity. PMID: 27288827
4. findings support the role of MC3R genetic variants in adiposity gain during early childhood. PMID: 26663875
5. There is no evidence of any association between MC3R variations and obesity. PMID: 26782456
6. Replacing murine Mc3r with and double-mutant (C17A+G241A) human MC3R showed greater weight and fat mass, increased energy intake and feeding efficiency. PMID: 26818770
7. the DPLIY motif and helix 8 was important for MC3R activation and signal transduction. The data led to a better understanding of the structure-function relationship of MC3R. PMID: 26220347
8. novel data about the structure-function relationship of MC3R, identifying residues important for receptor function; some studied mutations exhibited biased signaling, preferentially activating one intracellular signaling pathway. PMID: 25798062
9. propose three potential human candidate genes for voluntary physical exercise levels (MC3R, CYP24A1, and GRM8). PMID: 24821406
10. The cytoplasmic end of transmembrane domain 3 and the intracellular loop 2 were critical for MC3R function. PMID: 25228159
11. MC3R polymorphism is marginally associated in the development of pulmonary tuberculosis in Korean population. PMID: 25064630
12. MC3R is a 2-exon gene that requires a 5' UTR for translation, localization, and potential interaction with MRAP2 PMID: 25051171
13. 3' RACE experiments using MC3R transcript indicated the 3' UTR terminates approximately 115-160 bases after the translational stop codon. PMID: 25450386
14. This study focused on the search for the MC3R polymorphism in the Polish population. PMID: 24142065
15. Overall, the total prevalence of rare MC3R variants was 1 % in Belgian obese children and adolescents compared to 1.02 % in lean controls. PMID: 23264184
16. Suggest MC3R rs6127698 polymorphism is associated with pulmonary tuberculosis in a sample Iranian population. PMID: 23827504
17. Data suggest that specific amino acid residues (M247, R252, H254, K256, R257, A259) in 3rd intracellular loop (ICL3) of MC3R are important for ligand binding/signal transduction; studies used mutant, recombinant MC3R expressed in HEK293T cell line. PMID: 23323615
18. while MC3R mutations are unlikely to result in an autosomal dominant form of monogenic obesity given lack of strong cosegregation in family studies, the studies provided evidence that MC3R can be one of the genes which contributes to increased adiposity [review] PMID: 23280863
19. results suggest MC3R rs6127698 has no direct role in tuberculosis susceptibility. The possibility remains that this polymorphism is linked to an adjacent functional genetic variant, acting as a surrogate marker for disease risk PMID: 23497691
20. we provided detailed data of these novel human MC3R mutations leading to a better understanding of structure-function relationship of MC3R and the role of MC3R mutation in obesity PMID: 22884546
21. Interaction of the melanocortin 3 receptor (MC3R) and the growth hormone secretagogue receptor (GHSR)-1a results in a modulation of function in both receptors. PMID: 22327910
22. The polymorphism T6K is not located in the coding region of the human MC3R and has no influence on translation initiation which makes an impact on body weight unlikely. PMID: 22433616
23. Carriers of the MC3R 6Lys-81Ile haplotype showed higher respiratory quotient and higher glucose oxidation compared with non-carriers after standardization for fat-free mass. PMID: 21983807
24. Extracellular cysteine residue C305, C311 and C313 are crucial for receptor expression and the transmembrane cysteine residue, C115 and 162 are important for ligand binding and signaling. PMID: 22079958
25. in the populations studied functionally significant MC3R variants are associated with obesity PMID: 21047972
26. The study provided overall sufficient evidence to support that there is no major effect of genetic variants of MC3R and differential weight loss. PMID: 21695122
27. We demonstrated that the MC3R polymorphisms have a protective effect on metabolic traits. PMID: 21920079
28. Polymorphisms in MC3R promoter and CTSZ 3'UTR are associated with tuberculosis susceptibility. PMID: 21368909
29. A role of the MC3R gene in the pathogenesis of obesity in a small subset of patients. PMID: 20539302
30. While MC3R is an important regulator of energy homeostasis, mutations in the MC3R gene remain controversially associated with human obesity pathogenesis.[Review] PMID: 20882712
31. data are consistent with the involvement of rs3746619 in weight regulation among obese individuals PMID: 20972733
32. There is not sufficient evidence to support the contribution for common melanocortin-3 receptor variants in childhood obesity. However, our results are concordant for a role of melanocortin-3 receptor variants in some dimensions of eating behavior. PMID: 20144537
33. A novel melanocortin 3 receptor gene (MC3R) mutation associated with severe obesity. PMID: 11889220
34. An association between an insertion polymorphism was observed with fat mass, percent body fat, and total abdominal fat. PMID: 12142547
35. variaton in a Maori kindred with obesity and early onset type 2 diabetes PMID: 12161058
36. functional characterization of the I183N mutated MC3R compared with that of the wild-type MC3R after transfection in HEK293 cells PMID: 15276649
37. MC3R mutation might be genetic factor that confers susceptibility to obesity, likely due to haploinsufficiency. We identify a residue that is critical for activation of G protein-coupled receptors. PMID: 15292330
38. Single-nucleotide polymorphisms found in anorexia nervosa. PMID: 16314751
39. Our results suggest that TM3 and TM6 are important for NDP-MSH binding, while D121 in TM2 and D332 in TM7 are crucial for receptor activity and signaling.and thus provide molecular determinants of hMC3R responsible for ligand binding and receptor signals PMID: 16430209
40. in addition to its inverse agonistic activities, Agrp exhibits agonistic properties on the endocytosis pathway of melanocortin-3 and -4 receptors PMID: 17041250
41. SNPs of MC3R may regulate substrate oxidation and first-phase insulin secretion. PMID: 17192297
42. results suggest a gene-diet interaction between the MC3R C17A and G241A variants and a weight loss program for the ability to lose weight in childhood obesity PMID: 17413091
43. Further structure-activity studies of lactam derivatives of MT-II and SHU-9119 were made at MC3R. PMID: 17482720
44. MC3R mutations may not result in autosomal dominant forms of obesity but may contribute as a predisposing factor to childhood obesity. PMID: 17639020
45. highly conserved N/DPxxY motif, was critical for multiple aspects of the MC3R function, including cell surface expression, ligand binding, and signaling. PMID: 17964765
46. In the Maori kindred, the D20S32e polymorphism is significantly associated with insulin resistance but not with the metabolic syndrome. PMID: 18180070
47. in humans, MC3R mutations may be a cause of a dominantly inherited form of obesity PMID: 18231126
48. there is a link between MC3R and cell growth pathways that may involve the alteration of AKT signaling pathway PMID: 18291523
49. unlikely that MC3R gene plays a major role in tuberculosis susceptibility in African populations PMID: 18420963
50. acidic residues in transmembrane (TM) domains 1 and 3 are important for ligand binding whereas the acidic residues in TMs 2 and 7 are important for both ligand binding and signaling PMID: 18614155
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亞細胞定位：

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

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

Brain, placental, and gut tissues.
數據庫鏈接：

HGNC: 6931

OMIM: 155540

KEGG: hsa:4159

STRING: 9606.ENSP00000243911

UniGene: Hs.248018

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