anti-Forkhead Box E3 (FOXE3) Antibodies

This intronless gene belongs to the forkhead family of transcription factors, which is characterized by a distinct forkhead domain. Additionally we are shipping FOXE3 Proteins (3) and FOXE3 Kits (2) and many more products for this protein.

list all antibodies Gene Name GeneID UniProt
FOXE3 2301 Q13461
FOXE3 30923 Q9QY14
FOXE3 171302  
How to order from antibodies-online
  • +1 877 302 8632
  • +1 888 205 9894 (toll-free)
  • Order online
  • orders@antibodies-online.com

Top anti-FOXE3 Antibodies at antibodies-online.com

Showing 10 out of 66 products:

Catalog No. Reactivity Host Conjugate Application Images Quantity Supplier Delivery Price Details
Human Rabbit Un-conjugated IHC, WB WB Suggested Anti-FOXE3 Antibody Titration:  0.2-1 ug/ml  Positive Control:  HepG2 cell lysate Human Spermatophore 100 μL Log in to see 2 to 3 Days
$289.00
Details
Human Rabbit Un-conjugated WB WB Suggested Anti-FOXE3 Antibody Titration: 0.2-1 ug/ml ELISA Titer: 1:62500 Positive Control: SH-SYSY cell lysate 100 μL Log in to see 2 to 3 Days
$289.00
Details
Human Rabbit Un-conjugated ELISA, WB Western blot analysis of extracts from K562 cells, using FOXE3 Antibody. The lane on the right is treated with the synthesized peptide. 100 μg Log in to see 2 to 3 Days
$302.50
Details
Human Rabbit Un-conjugated IHC, WB Immunohistochemical analysis of FOXE3 staining in human brain formalin fixed paraffin embedded tissue section. The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0). The section was then incubated with the a Western blot analysis of FOXE3 expression in SHSYSY (A), MDAMB435 (B) whole cell lysates. 200 μL Log in to see 13 to 14 Days
$487.50
Details
Human Rabbit Un-conjugated EIA, WB Western blot analysis of FOXE3 / FKHL12 Antibody (Center) in MDA-MB435 cell line lysates (35ug/lane). This demonstrates the FOXE3 antibody detected the FOXE3 protein (arrow). 0.4 mL Log in to see 6 to 8 Days
$390.50
Details
Human Rabbit Un-conjugated IHC, IHC (p), WB Human Brain, Cerebellum (formalin-fixed, paraffin-embedded) stained with FOXE3 antibody ABIN214754 at 5 ug/ml followed by biotinylated goat anti-rabbit IgG secondary antibody ABIN481713, alkaline phosphatase-streptavidin and chromogen. Human Testis (formalin-fixed, paraffin-embedded) stained with FOXE3 antibody ABIN214754 at 5 ug/ml followed by biotinylated goat anti-rabbit IgG secondary antibody ABIN481713, alkaline phosphatase-streptavidin and chromogen. 50 μg Log in to see 7 to 9 Days
$727.83
Details
Human Rabbit Un-conjugated WB FOXE3 Antibody (Center) (ABIN656110) western blot analysis in MDA-MB435 cell line lysates (35 µg/lane). This demonstrates the FOXE3 antibody detected the FOXE3 protein (arrow). 400 μL Log in to see 10 to 11 Days
$335.50
Details
Human Rabbit Un-conjugated WB 50 μg Log in to see 7 to 9 Days
$551.83
Details
Human Rabbit Un-conjugated WB Western blot analysis in MDA-MB435 cell line lysates (35ug/lane). 400 μL Log in to see 2 to 3 Days
$515.63
Details
Human Rabbit Un-conjugated ELISA, IHC, WB 100 μL Log in to see 16 Days
$181.73
Details

FOXE3 Antibodies by Reactivity, Application, Clonality and Conjugate

Attributes Applications Host Clonality Conjugate
Human , ,
,

, , , , , , , , , , , , , , , ,
Mouse (Murine) , ,


, , , , , , , , , , , , ,
Rat (Rattus) ,


, , , , , , , , , , , , ,

More Antibodies against FOXE3 Interaction Partners

Zebrafish Forkhead Box E3 (FOXE3) interaction partners

  1. Data demonstrate that Foxe3 is necessary for lens development in zebrafish and that foxe3 lies genetically downstream of pitx3 (show PITX3 Antibodies) in a zebrafish lens development pathway.

  2. foxe3 function is necessary for the execution of lens-specific gene expression and lens morphogenesis.

Human Forkhead Box E3 (FOXE3) interaction partners

  1. Data show that DnaJ (Hsp40 (show DNAJB1 Antibodies)) homolog (show DNAJB4 Antibodies), subfamily B (show CYP Antibodies), member 1 (DNAJB1 (show DNAJB1 Antibodies)) 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.

  2. Although congenital aphakia (show PITX3 Antibodies) 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.

  3. 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.

  4. FOXE3 mutations lead to a reduced number of aortic smooth muscle cells (SMCs) during development and increased SMC (show DYM Antibodies) apoptosis in the ascending aorta in response to increased biomechanical forces.

  5. This is the first functional evidence demonstrating that FOXE3 mutations identified in patients impair protein function with differential effects.

  6. 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.

  7. This study demonstrates that a cluster of patients with sclerocornea, aphakia (show PITX3 Antibodies), and microphthalmia in a small Mexican village is due to a FOXE3 p.Y98H founder mutation.

  8. 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.

  9. 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.

  10. Autosomal-dominant mutations within FOXE3 cause anterior segment dysgenesis and has important clinical utility, especially for the diagnosis of mildly affected patients.

Mouse (Murine) Forkhead Box E3 (FOXE3) interaction partners

  1. These results clearly show that the development of early-onset cataracts requires at least two mutant alleles of Foxe3(rct) and Pde6b(rd1 (show PDE6B Antibodies)), and another modifier associated with the severity of cataract phenotypes in Foxe3(rct) mice underlies the genetic backgrounds in mice.

  2. The Hedgehog (show SHH Antibodies) pathway with its member Smoothened is required during a discrete embryonic period (E9.5-E12.5) in lens development to regulate lens epithelial cell proliferation, survival and FoxE3 expression.

  3. Foxe3 as a transcriptional target of Pitx3 (show PITX3 Antibodies) explains at least in part some of the phenotypic similarities of the ak and dyl mice (dysgenic lens, a Foxe3 allele).

  4. The observed changes in the expression of FoxE3 suggest that Msx2 is an important contributor in controlling transcription of target genes critical for early eye development.

  5. the ectopic activation of downstream effectors of the hedgehog (show SHH Antibodies) signaling pathway in the mouse lens disrupts normal fiber cell differentiation by a mechanism consistent with a sustained epithelial cellular developmental program driven by FoxE3.

  6. cataracts in rct mice are caused by reduced Foxe3 expression in the lens and this decreased expression is a result of a deletion in a cis (show CISH Antibodies)-acting regulatory element

  7. Foxe3 promoter was activated by Sip1 (show ZEB2 Antibodies)

  8. targeted disruption of Foxe3 results in abnormal development of the eye. Cells of the anterior lens epithelium show a decreased rate of proliferation, resulting in a smaller than normal lens.

  9. early Foxe3 expression is sensitive to halved Pax6 (show PAX6 Antibodies) gene dosage & there is phenotypic similarity between Pax6 (show PAX6 Antibodies) & Foxe3 mutants; we propose that many ocular malformations associated with Pax6 (show PAX6 Antibodies) haploinsufficiency are consequences of reduced Foxe3 expression

  10. Proper inactivation of FoxE3 expression at the lens equator is important for many aspects of fiber differentiation, and persistent expression leads to a partial epithelialization of fiber cells, with severe consequences for lens function.

FOXE3 Antigen Profile

Protein Summary

This intronless gene belongs to the forkhead family of transcription factors, which is characterized by a distinct forkhead domain. The protein encoded functions as a lens-specific transcription factor and plays an important role in vertebrate lens formation. Mutations in this gene are associated with anterior segment mesenchymal dysgenesis and congenital primary aphakia.

Gene names and symbols associated with anti-Forkhead Box E3 (FOXE3) Antibodies

  • forkhead box E3 (foxe3) antibody
  • forkhead box E3 (FOXE3) antibody
  • forkhead box E3 (LOC100301611) antibody
  • forkhead box E3 (Foxe3) antibody
  • forkhead box E3 L homeolog (foxe3.L) antibody
  • dyl antibody
  • FKHL12 antibody
  • FOXE3 antibody
  • foxe4 antibody
  • FREAC-8 antibody
  • FREAC8 antibody
  • HFH7 antibody
  • HNF3 antibody
  • lens1 antibody
  • lens1-A antibody
  • rct antibody

Protein level used designations for anti-Forkhead Box E3 (FOXE3) Antibodies

forkhead box protein E3 , forkhead box E3 , FREAC-8 , forkhead, drosophila, homolog-like 12 , forkhead-related protein FKHL12 , forkhead-related transcription factor 8 , Rinshoken cataract , dysgenetic lens , hepatocyte nuclear factor 3 forkhead homolog 7 , forkhead box protein E4 , forkhead protein lens1 , xlens1

GENE ID SPECIES
570855 Danio rerio
772006 Gallus gallus
100301611 Oryzias latipes
2301 Homo sapiens
30923 Mus musculus
171302 Rattus norvegicus
373809 Xenopus laevis
610277 Canis lupus familiaris
787258 Bos taurus
Selected quality suppliers for anti-FOXE3 (FOXE3) Antibodies
Did you look for something else?