FOXE3 Antibody

說明書

中文名稱：

FOXE3兔多克隆抗體
貨號：

CSB-PA008302
規格：

￥1090
圖片：
Western Blot analysis of K562 cells using FoxE3 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.：

Q13461
基因名：

FOXE3
別名：

Drosphilia Forkhead Homolog Like 12 antibody; FKHL 12 antibody; FKHL12 antibody; Forkhead Box E3 antibody; Forkhead box protein E3 antibody; Forkhead Related Activator 8 antibody; Forkhead related protein FKHL12 antibody; Forkhead-related protein FKHL12 antibody; Forkhead-related transcription factor 8 antibody; Foxe3 antibody; FOXE3 forkhead box E3 antibody; FOXE3_HUMAN antibody; FREAC 8 antibody; FREAC-8 antibody; FREAC8 antibody
宿主：

Rabbit
反應種屬：

Human,Mouse,Rat
免疫原：

Synthesized peptide derived from the Internal region of Human FoxE3.
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, IHC, ELISA

推薦稀釋比：

Application	Recommended Dilution
WB	1:500-1:2000
IHC	1:100-1:300
ELISA	1:20000

Protocols：

Western Blotting (WB) Protocol
Immunohistochemistry (IHC) 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：

Transcription factor that controls lens epithelial cell growth through regulation of proliferation, apoptosis and cell cycle. During lens development, controls the ratio of the lens fiber cells to the cells of the anterior lens epithelium by regulating the rate of proliferation and differentiation. Controls lens vesicle closure and subsequent separation of the lens vesicle from ectoderm. Controls the expression of DNAJB1 in a pathway that is crucial for the development of the anterior segment of the eye.
基因功能參考文獻：
1. The sclerocornea-microphthalmia-aphakia complex is a severe malformative ocular phenotype resulting from mutations in the FOXE3 transcription factor. To date, patients from at least 14 families with this uncommon ocular disorder have been described. The identification of 2 novel pathogenic variants in our patients expands the mutational spectrum in FOXE3-related congenital eye disorders. PMID: 29878917
2. Data show that DnaJ (Hsp40) homolog, subfamily B, member 1 (DNAJB1) is a transcriptional target of forkhead box protein E3 (FOXE3) in a pathway that is crucial for the development of the anterior segment of the eye. PMID: 27218149
3. Although congenital aphakia is known to be caused by mutations in the FOXE3 gene, the results of lack of coding mutation in this patient suggests a possible genetic heterogeneity of the disease. PMID: 28805541
4. Only one novel missense mutation in exon 1 of FOXE3 (Chr1:47,882,459, c.472G>C, p.Gly158Arg) was identified being homozygous in the three affected and heterozygous in the two unaffected, which was confirmed by Sanger sequencing. PMID: 27669367
5. FOXE3 mutations lead to a reduced number of aortic smooth muscle cells (SMCs) during development and increased SMC apoptosis in the ascending aorta in response to increased biomechanical forces. PMID: 26854927
6. This is the first functional evidence demonstrating that FOXE3 mutations identified in patients impair protein function with differential effects. PMID: 25504734
7. Our results indicate that the FOXE3 p.Val201Met allele is associated with eye defects (OR = 3.5), suggesting its involvement as an ocular malformation risk factor. PMID: 24689660
8. This study demonstrates that a cluster of patients with sclerocornea, aphakia, and microphthalmia in a small Mexican village is due to a FOXE3 p.Y98H founder mutation. PMID: 24019743
9. shRNA-mediated gene silencing of FOXE3 could significantly inhibit cell growth and induce the G1-phase arrest in human lens epithelial cell line-3 cells. PMID: 22527307
10. The FOXE3 mutation detected in c.601 G > A, predicting p.Val201Met which were not yet been included in public databases, but has previously been reported in both A/M patients. PMID: 22204637
11. Autosomal-dominant mutations within FOXE3 cause anterior segment dysgenesis and has important clinical utility, especially for the diagnosis of mildly affected patients. PMID: 21150893
12. Using autoantibodies from systemic sclerosis (SSc) patients, two anti-CENP-A-specific motifs were defined in its immunodominant epitope Ap17-30. One of these motifs matched residues 53-62 of FOXE3, a protein not previously implicated in SSc. PMID: 20630806
13. This is the fourth report detailing homozygous FOXE3 mutations causing anterior segment abnormalities in human patients. PMID: 20664696
14. Mutations in several transcription factors associated with aniridia and congenital cataract, FOXE3, (PAX6), PITX2, and PITX3 genes, were examined. PMID: 20806047
15. FOXE3 is responsible for the early developmental arrest of the lens placode, and the complete loss of a functional FOXE3 protein results in primary aphakia. PMID: 20361012
16. Recessive mutations in FOXE3 were found in four of 26 probands affected with bilateral microphthalmia (15% of all bilateral microphthalmia and 100% of consanguineous families with this phenotype). PMID: 20140963
17. Role very early in the lens developmental program, perhaps earlier than any role recognized elsewhere for this gene. PMID: 16826526
18. findings suggest that mutations in FOXE3 can give rise to a broad spectrum of eye anomalies, largely, but not exclusively related to lens development, and that both dominant and recessive inheritance patterns can be represented PMID: 19708017
19. FOXE3 is essential for closure of the lens vesicle during eye development and for lens epithelial survival and proliferation. PMID: 10652278
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相關疾病：

Anterior segment dysgenesis 2 (ASGD2); Cataract 34, multiple types (CTRCT34); Aortic aneurysm, familial thoracic 11 (AAT11)
亞細胞定位：

Nucleus.
數據庫鏈接：

HGNC: 3808

OMIM: 601094

KEGG: hsa:2301

STRING: 9606.ENSP00000334472

UniGene: Hs.112968

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