FOXE1 Antibody

中文名稱：

FOXE1兔多克隆抗體
貨號：

CSB-PA008811LA01HU
規格：

￥440
圖片：
Western Blot
Positive WB detected in: Mouse kidney tissue, Mouse brain tissue
All lanes: FOXE1 antibody at 2.4μg/ml
Secondary
Goat polyclonal to rabbit IgG at 1/50000 dilution
Predicted band size: 39 kDa
Observed band size: 39 kDa

Immunofluorescent analysis of Hela cells using CSB-PA008811LA01HU 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) FOXE1 Polyclonal antibody
Uniprot No.：

O00358
基因名：

FOXE1
別名：

FKH L15 antibody; FKHL 15 antibody; FKHL15 antibody; Forkhead (Drosophila) like 15 antibody; Forkhead box E1 antibody; Forkhead box E2 antibody; Forkhead box protein E1 antibody; Forkhead box protein E2 antibody; Forkhead drosophila homolog like 15 antibody; Forkhead like 15 antibody; Forkhead related protein FKHL 15 antibody; Forkhead related protein FKHL15 antibody; Forkhead-related protein FKHL15 antibody; FOX E1 antibody; FOX E2 antibody; FOXE 1 antibody; FOXE 2 antibody; FOXE1 antibody; FOXE1_HUMAN antibody; FOXE2 antibody; HFKH 4 antibody; HFKH4 antibody; HFKL 5 antibody; HFKL5 antibody; HNF-3/fork head-like protein 5 antibody; Thyroid transcription factor 2 antibody; TITF 2 antibody; TITF2 antibody; TTF 2 antibody; TTF-2 antibody; TTF2 antibody
宿主：

Rabbit
反應種屬：

Human, Mouse
免疫原：

Recombinant Human Forkhead box protein E1 protein (184-365AA)
免疫原種屬：

Homo sapiens (Human)

標記方式：

Non-conjugated

本頁面中的產品，FOXE1 Antibody (CSB-PA008811LA01HU)，的標記方式是Non-conjugated。對于FOXE1 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-PA008811LB01HU	FOXE1 Antibody, HRP conjugated	ELISA
FITC	CSB-PA008811LC01HU	FOXE1 Antibody, FITC conjugated
Biotin	CSB-PA008811LD01HU	FOXE1 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, WB, IF

推薦稀釋比：

Application	Recommended Dilution
WB	1:500-1:5000
IF	1:50-1:200

Protocols：

ELISA Protocol
Western Blotting (WB) 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：

Transcription factor that binds consensus sites on a variety of gene promoters and activate their transcription. Involved in proper palate formation, most probably through the expression of MSX1 and TGFB3 genes which are direct targets of this transcription factor. Also implicated in thyroid gland morphogenesis. May indirectly play a role in cell growth and migration through the regulation of WNT5A expression.
基因功能參考文獻：
1. We confirmed the association of FOXE1 gene and cleft lip with or without cleft palate by a family based study. For the first time, rs1867277 was significantly associated with cleft lip with or without cleft palate PMID: 29509083
2. Mutations of TTF2 is associated with risk of Papillary Thyroid Cancer in Chinese. Patients with Multiplendular goiter and no metastasis are more likely to suffer PTC. G/A mutation of TTF2 had a high correlation with PTC in the overall population. PMID: 26356687
3. Report that PTCSC2 binds myosin-9 (MYH9). In a bidirectional promoter shared by FOXE1 and PTCSC2, MYH9 inhibits the promoter activity in both directions. This inhibition can be reversed by PTCSC2, which acts as a suppressor. PMID: 28049826
4. replication confirmed at genome-wide significance the association of loci at FOXE1 with hypothyroidism, and PDE8B, CAPZB and PDE10A with serum TSH. A total of 12 SNPs seemed to explain nearly 7% of the serum TSH variation PMID: 28727628
5. The functional variants rs965513 and rs1867277 independently contribute to genetic predisposition to papillary thyroid carcinoma, while a contributing role of the FOXE1 poly-Ala polymorphism could not be confirmed. PMID: 27824288
6. FOXE1 interacts with ELK1 on thyroid relevant gene promoters, establishing a new regulatory pathway for its role in adult thyroid function. Co-regulation of TERT suggests a mechanism by which allelic variants in/near FOXE1 are associated with thyroid cancer risk. PMID: 27852061
7. In a Cuban population, differentiated thyroid cancer risk was positively and strongly associated with the number of copies in the minor allele (A) for SNP rs965513 near FOXE1 among people who consumed less iodine than the median. PMID: 27610545
8. methylation-mediated silencing of FOXE1 expression may contribute to the progression of CRC. PMID: 27271927
9. The rs965513 polymorphism is a risk factor for thyroid cancer.[meta-analysis] PMID: 27191655
10. Patient-related factors modify the predisposition to papillary thyroid carcinoma by increasing the risk for rs944289 (near the NKX2-1 locus) per year of age, and by enhancing the protective effect of the FOXE1 GGT haplotype in men. PMID: 28660995
11. We identified a FOXE1: c.532_537delGCCGCC p.(Ala178_Ala179del) variant that predisposes to thyroid ectopia. Taken together, this is the first report of mosaic 11p13 deletion in association with thyroid dysgenesis PMID: 28398607
12. Our results implicate FOXE1 as an important locus whose polymorphic variation increases risks for all types of isolated clefts, and opens a new biological pathway to investigate in efforts to understand genetic factors underlying human clefting. PMID: 27604706
13. FOXE1 polyalanine repeat polymorphisms are associated with thyroid cancer, but only for tumours larger than 1 cm, suggesting a role in disease progression. PMID: 27474100
14. In the analysis of all OFCs combined, SNPs near FOXE1 reached genome-wide significance PMID: 28054174
15. FOXE1 was the only gene which was over-expressed in six out of eight lung cancer cell lines and human cancer tissue specimens and is an important regulator by targeting autophagy and Matrix Metalloproteinases pathways in lung cancer development. PMID: 27755953
16. Taken together, this study showed that rs7043516 may be considered as a potentially susceptible marker of cleft lip only among Chinese Han populations. PMID: 26728781
17. this study shows that FOXE1 polymorphism is strongly associated with non-syndromic cleft lip and palate in populations in northeast China PMID: 26100861
18. High Levels of mRNA of both FOXE1 are associated with benign than in malignant thyroid lesions. PMID: 26370671
19. Our findings suggest that FOXE1 variations generate a higher risk for poor histopathological features of papillary thyroid carcinoma PMID: 26722557
20. genetic susceptibility to thyroid cancer seems likely to be associated with the risk alleles at rs1867277, rs965513, rs1443434, and rs907580 PMID: 26206751
21. analysis of novel somatic mutations of FOXE1 in papillary thyroid cancer PMID: 25950909
22. Causal mutations for orofacial clefting and thyroid diseases occur within cis-regulatory elements at the human FOXE1 locus. PMID: 25652407
23. In pancreatic cancer cells, AF6 is expressed at reduced levels, causing Dvl2 to be upregulated and available to bind and enhance FOXE1-induced trans-activation of Snail, which promotes proliferation and metastasis. PMID: 26013125
24. FOXE1 germline rare variant is involved in familal non-medullary thyroid carcinoma. PMID: 25381600
25. our data suggest that SYNE1 and FOXE1 are promising markers for colorectal cancer detection. PMID: 25538088
26. Our data suggest a role for PTCSC2, FOXE1, and TSHR in the predisposition to papillary thyroid carcinoma. PMID: 25303483
27. Findings suggest that the SNPs in XKR4 and near FOXE1 are involved in the regulation of TSH levels. PMID: 24852370
28. study identifies probable susceptibility variants of FOXE1 for oral clefts in the Thai population PMID: 24252547
29. genetic association studies in population in Germany: Data suggest that an SNP in FOXE1 (rs965513) is associated with increased risk for differentiated thyroid cancer (of an aggressive nature) in the population studied. PMID: 24325646
30. FOXE1 and SYNE1 hypermethylation markers demonstrated significantly increased expression in neoplastic tissue. PMID: 24280874
31. Common variations of FOXE1 are a risk factor associated with increased thyroid cancer susceptibility. PMID: 24489898
32. The current meta-analysis provided evidence that FOXE1 genetic polymorphisms may contribute to increased papillary thyroid carcinoma risk..ATM genetic polymorphisms may not be important dominants of susceptibility to this neoplasm. PMID: 24756757
33. three common variations on FOXE1 is a risk factor associated with increased thyroid cancer susceptibility, but these associations vary in different ethnic populations PMID: 24744143
34. A tissue-dependent differentially methylated regions (DMR) in the FOXE1 promoter. This DMR contains two consecutive CpG dinucleotides, which are epigenetic modifiers of FOXE1 expression in nontumoral tissues. PMID: 24646064
35. These results strongly support the FOXE1 locus as a risk factor for nsOFC. With the data of the initial study, there is now considerable evidence that this locus is the first conclusive risk factor shared between nsCL/P and nsCPO. PMID: 24563486
36. Significant association with PTC was found for rs1801516 (D1853N) in ATM and rs1867277 in the promoter region of FOXE1 (OR = 1.55, 95% CI 1.03, 2.34). PMID: 24105688
37. single nucleotide polymorphisms at 9q22.33 near FOXE1 showed convincing evidence of association with nonmedullary thyroid carcinoma risk in high-risk families PMID: 24127282
38. Nuclear FOXE1 expression in tumor cells in vicinity of the PTC border is associated with presence of a risk allele of rs1867277 (c.-238G>A) in the 5' untranslated region of the FOXE1 gene, as well as with pathological characteristics of PTC. PMID: 23327367
39. the FOXE1 gene exhibits significant differential expression levels between PTC tissues and adjacent non-tumor thyroid tissues. PMID: 23715628
40. In addition, eight genes classified as 'second tier' hits in the original study (PAX7, THADA, COL8A1/FILIP1L, DCAF4L2, GADD45G, NTN1, RBFOX3 and FOXE1) showed evidence of linkage and association in this replication sample. PMID: 23512105
41. study showed evidence of association between forkhead box E1 (FOXE1) variants and thyroid cancer risk in the Portuguese population PMID: 22882326
42. coding polyalanine expansion in FOXE1 may be responsible for the observed association between FOXE1 and papillary thyroid cancer PMID: 22736773
43. FOXE1 genes suggest a role for orofacial clefting in hispanic polulation. PMID: 22753311
44. Novel associations for hypothyroidism and autoimmune risk loci include SNPs near the FOXE1 gene. PMID: 22493691
45. Polyalanine repeat expansions in FOXE1 is associated with the genetic aetiology of POF in Chinese women. PMID: 22177572
46. Both FOXE1 and NKX2-1 were associated with the increased risk of sporadic Japanese PTC. PMID: 21730105
47. these results excluded the association of poly (Ala) polymorphism with autoimmune thyroid diseases; however it confirms the involvement of FOXE1 in the genesis of thyroid carcinoma. PMID: 21896990
48. FOXE1-polyAla tract expansion may contribute to the molecular background of familial but not sporadic forms of thyroid hemiagenesis. PMID: 21311165
49. Polymorphisms in TIMP2 and WNT9B are novel loci predisposing to cleft palate. PMID: 21462296
50. Effects of genetic variation in FOXE1 on serum free thyroxine (FT4) levels in Caucasian populations are demonstrated, as well as borderline significant effects on serum thyroid hormone (TSH) levels. PMID: 21367965
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相關疾病：

Bamforth-Lazarus syndrome (BLS); Thyroid cancer, non-medullary, 4 (NMTC4)
亞細胞定位：

Nucleus.
組織特異性：

Detected in adult brain, placenta, lung, liver, skeletal muscle, kidney, pancreas, heart, colon, small intestine testis and thymus. Expression was strongest in heart and pancreas.
數據庫鏈接：

HGNC: 3806

OMIM: 241850

KEGG: hsa:2304

STRING: 9606.ENSP00000364265

UniGene: Hs.159234

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