MTNR1B Antibody

中文名稱：

MTNR1B兔多克隆抗體
貨號：

CSB-PA015190LA01HU
規格：

￥440
圖片：
Immunohistochemistry of paraffin-embedded human eye tissue using CSB-PA015190LA01HU at dilution of 1:100

Immunohistochemistry of paraffin-embedded human brain tissue using CSB-PA015190LA01HU at dilution of 1:100

Immunofluorescent analysis of HepG2 cells using CSB-PA015190LA01HU at dilution of 1:100 and Alexa Fluor 488-congugated AffiniPure Goat Anti-Rabbit IgG(H+L)
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) MTNR1B Polyclonal antibody
Uniprot No.：

P49286
基因名：

MTNR1B
別名：

MTNR1B; Melatonin receptor type 1B; Mel-1B-R; Mel1b receptor
宿主：

Rabbit
反應種屬：

Human
免疫原：

Recombinant Human Melatonin receptor type 1B protein (1-42AA)
免疫原種屬：

Homo sapiens (Human)

標記方式：

Non-conjugated

本頁面中的產品，MTNR1B Antibody (CSB-PA015190LA01HU)，的標記方式是Non-conjugated。對于MTNR1B Antibody，我們還提供其他標記。見下表：

標記方式	貨號	產品名稱	應用
HRP	CSB-PA015190LB01HU	MTNR1B Antibody, HRP conjugated	ELISA
FITC	CSB-PA015190LC01HU	MTNR1B Antibody, FITC conjugated
Biotin	CSB-PA015190LD01HU	MTNR1B Antibody, Biotin conjugated	ELISA

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
應用范圍：

ELISA, IHC, IF

推薦稀釋比：

Application	Recommended Dilution
IHC	1:20-1:200
IF	1:50-1:200

Protocols：

ELISA Protocol
Immunohistochemistry (IHC) Protocol
Immunofluorescence (IF) 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：

High affinity receptor for melatonin. Likely to mediate the reproductive and circadian actions of melatonin. The activity of this receptor is mediated by pertussis toxin sensitive G proteins that inhibit adenylate cyclase activity.
基因功能參考文獻：
1. Genome-wide significant (P < 5 x 10(-8) ) interaction with MTNR1B and joint effects were detected for CMIP intronic rs17197883. PMID: 29691896
2. The reduced titer of melatonin, along with altered fasting blood glucose due to MTNR1B genetic variant, acts as a risk factor towards type 2 diabetes in the Gujarat population of India. PMID: 29674279
3. that MTNR1B and IRS2 gene variants impacted epicardial fat thickness, lipid profile and glucose homeostasis PMID: 28708046
4. melatonin stimulates PINK1 expression via an MT2 /Akt/NF-kappaB pathway, and such stimulation is important for the prevention of neuronal cell apoptosis under high glucose conditions. PMID: 28580603
5. MTNR1B rs10830963 polymorphism is associated with gestational diabetes susceptibility, and women with a higher number of G alleles have an increased risk of gestational diabetes development. PMID: 28084098
6. In women with psychosis, troponin T levels were associated with genetic variants in MTNR1B. PMID: 28167435
7. The present data suggested that MTNR1B polymorphisms could influence the clinical features in lupus patients, and especially the susceptibility to leucopenia PMID: 27115109
8. MTNR1B rs10830963/G variant is associated with gestational diabetes binary and glycemic traits in the Caucasian case-control study. PMID: 28072873
9. the risk allele (G allele) of rs10830963 and (T allele) of rs1387153 in MTNR1B lead to a higher risk for gestational diabetes mellitus PMID: 26563312
10. Our results provide the surprising insight that the MTNR1B risk allele influences dynamics of melatonin secretion, generating a novel hypothesis that the MTNR1B risk allele may extend the duration of endogenous melatonin production later into the morning and that early waking may magnify the diabetes risk conferred by the risk allele. PMID: 26868293
11. Insomnia does not mediate or modify the association between MTNR1B risk variant rs10830963 and glucose levels. PMID: 26912228
12. finding suggests that the MTNR1B-dependent vulnerability for elevated fasting plasma glucose levels is shared between bipolar disorder and schizophrenia PMID: 26991397
13. For the first time, we show that Cry 2 rs2292910 and MTNR1B rs3781638 are associated with osteoporosis in a Chinese geriatric cohort. PMID: 26564225
14. rs10830963 polymorphism was not associated with polycystic ovary syndrome in Han Chinese. PMID: 26519818
15. Authors investigated the association between rs4753426 single nucleotide polymorphisms in the melatonin receptor 1B (MTNR1B) gene and the risk of developing gestational diabetes mellitus (GDM). PMID: 26345809
16. Increases in islet MTNR1B expression is associated with type 2 diabetes susceptibility. PMID: 26551672
17. This systematic review was a comprehensive analysis of the currently available evidence, and found an overall significant association of rs4753426 polymorphism with the risk of--{REVIEW} PMID: 26431121
18. results indicate, for the first time, the presence of a functional circadian clock in the human myometrium with the hMTNR1B gene as a clock controlled target. PMID: 25939854
19. MTNR1B rs4753426 and MTNR1B rs10830963 polymorphisms are not obviously associated with risk of AIS in either Asian populations or Caucasian populations. PMID: 25898821
20. rs10830963 MTNR1B polymorphism could be associated with individual differences in weight loss induced by a hypocaloric diet PMID: 25870980
21. MTNR1B rs10830963 risk variant worsens the effect of melatonin on glucose tolerance PMID: 26440713
22. these observations suggest a biologically plausible season-dependent association between SNPs at CRY1, CRY2 and MTNR1B and glucose homeostasis. PMID: 25707907
23. It has been shown for the first time in obese youth that the MTNR1B variant is associated with an increased risk of IFG PMID: 25919927
24. our study found that the genetic polymorphisms rs10830963 and rs1387153 in MTNR1B and rs1801278 in IRS1 were associated with an increased risk of developing GDM. PMID: 25146448
25. Carriers of the G allele of MTNR1B rs10830963 are more likely to develop gestational diabetes than carriers of the C allele. PMID: 25982863
26. results obtained are suggestive of MTNR1B role in T2D etiology, they need to be confirmed with much larger sample sizes PMID: 25922310
27. cross-talk mediated via physical association of melatonin MT2 and 5-HT2C receptors into functional heteromers PMID: 25770211
28. The extent of receptor internalization for the human MT2 receptor is independent of the intrinsic efficacy of agonists and provide novel insights into the controversial relationship between intrinsic agonist efficacy and agonist-induced internalization PMID: 25059758
29. the association between the common MTNR1B rs10830963 variation and fasting plasma glucose levels in BH population. PMID: 24710643
30. We conclude that variation in MTNR1B contributes to the absolute level of insulin secretion but not to differences in the temporal rate of change in insulin secretion. PMID: 24728128
31. High expression for MT2 receptor is associated with gastric adenocarcinoma. PMID: 24142542
32. 14 mutants with loss of Gi protein activation that associate with increased risk of type 2 diabete development (Review) PMID: 23798576
33. Genetics of MTNR1B point to impact of the melatonin signalling pathway for BP and left ventricular function. PMID: 23611530
34. GCKR rs780094 variant confers high cross-ethnicity risk for the development of T2DM, while significant associations between GCK, MTNR1B and G6PC2 variants and T2DM risk are limited to Caucasians. PMID: 23840762
35. Our data indicate that variants in the circadian-related genes CRY2 and MTNR1B may affect long-term changes in energy expenditure, and dietary fat intake may modify the genetic effects. PMID: 24335056
36. genetic association study in women in Finland: Data suggest that 2 SNPs in MTNR1B (rs10830963; rs1387153) are associated with gestational diabetes (and type 2 diabetes, as shown in previous studies); down-regulation of insulin secretion is related. PMID: 23761423
37. The rs10830963 MTNR1B polymorphism is a risk factor for developing impaired glucose regulation and type 2 diabetes mellitus. (Meta-analysis) PMID: 23226241
38. There is a strong association of rs1374645 polymorphism with low fasting blood glucose levels in the low BMI group compared to the high BMI group. PMID: 21558052
39. Investigated whether genetic variants in MTNR1B were associated with delirium; none of the 5 single nucleotide polymorphisms tested were found to be associated with the occurrence of delirium. PMID: 22759724
40. The MTNR1B is likely to be involved in the regulation of glucose homeostasis during pregnancy. PMID: 22768333
41. These data showing the association of polymorphisms in the TPH2 and MTNR1B genes with the progressive subtypes of multiple sclerosis and disability suggest dysregulation in melatonin pathway PMID: 22698518
42. This study confirms the association of gestational diabetes mellitus with the rs10830963 variant in a sample of the Greek population. PMID: 22450346
43. Rare MTNR1B variants impairing melatonin receptor 1B function contribute to type 2 diabetes. PMID: 22286214
44. Six SNP(rs7754840 in CDKAL1, rs391300 in SRR, rs2383208 in CDKN2A/2B, rs4402960 in IGF2BP2, rs10830963 in MTNR1B, rs4607517 in GCK)risk alleles of type 2 diabetes were associated with GDM in pregnant Chinese women. PMID: 22096510
45. The results of this study suggested that the Single nucleotide polymorphisms MT(2) receptor gene influence the risk of recurrent depressive disorder. PMID: 21353709
46. The rs10830963 polymorphism in MTNR1B was associated with increased fasting glucose and risk of impaired fasting glucose in Chinese children and adolescents. PMID: 21701235
47. The G-allele of rs10830693 in the MTNR1B gene was significantly related to glucose levels, while an impact of this genetic variant on the changes in glucose metabolism in children participating in a lifestyle intervention was not observable. PMID: 21366812
48. There is no effect by the common gene variant rs10830963 of the melatonin receptor 1B on the association between sleep disturbances and type 2 diabetes. PMID: 21380592
49. There were significant associations between the two genetic variants (rs10830963 and rs1387153) of the melatonin receptor 1B gene and gestational diabetes mellitus. PMID: 21658282
50. The rs3781637 A/G polymorphism of the MTNR1B gene is associated with type 2 diabetes, plasma, total cholesterol and LDL-C levels in the Han Chinese population. PMID: 21470412
顯示更多

收起更多
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：

Expressed in retina and less in brain and hippocampus.
數據庫鏈接：

HGNC: 7464

OMIM: 600804

KEGG: hsa:4544

STRING: 9606.ENSP00000257068

UniGene: Hs.569039

Most popular with customers

YWHAG Recombinant Monoclonal Antibody

Applications: ELISA, WB, IHC

Species Reactivity: Human
YWHAB Recombinant Monoclonal Antibody

Applications: ELISA, WB, IHC, IF, FC

Species Reactivity: Human, Mouse, Rat
XRCC5 Recombinant Monoclonal Antibody

Applications: ELISA, WB, IHC, IF

Species Reactivity: Human
XPNPEP1 Recombinant Monoclonal Antibody

Applications: ELISA, IHC, FC

Species Reactivity: Human
XDH Recombinant Monoclonal Antibody

Applications: ELISA, WB, IHC

Species Reactivity: Human
WT1 Recombinant Monoclonal Antibody

Applications: ELISA, WB, IHC

Species Reactivity: Human
WFDC2 Recombinant Monoclonal Antibody

Applications: ELISA, WB, FC

Species Reactivity: Human
VIM Recombinant Monoclonal Antibody

Applications: ELISA, IHC, IF

Species Reactivity: Human