FOXE3 Antibody (Center) Blocking peptide
Synthetic peptide
- SPECIFICATION
- CITATIONS
- PROTOCOLS
- BACKGROUND
Primary Accession | Q13461 |
---|---|
Clone Names | 101109021 |
Gene ID | 2301 |
---|---|
Other Names | Forkhead box protein E3, Forkhead-related protein FKHL12, Forkhead-related transcription factor 8, FREAC-8, FOXE3, FKHL12, FREAC8 |
Format | Peptides are lyophilized in a solid powder format. Peptides can be reconstituted in solution using the appropriate buffer as needed. |
Storage | Maintain refrigerated at 2-8°C for up to 6 months. For long term storage store at -20°C. |
Precautions | This product is for research use only. Not for use in diagnostic or therapeutic procedures. |
Name | FOXE3 |
---|---|
Synonyms | FKHL12, FREAC8 |
Function | Transcription factor that controls lens epithelial cell growth through regulation of proliferation, apoptosis and cell cycle (PubMed:22527307, PubMed:25504734). 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 (By similarity). Controls lens vesicle closure and subsequent separation of the lens vesicle from ectoderm (By similarity). Controls the expression of DNAJB1 in a pathway that is crucial for the development of the anterior segment of the eye (PubMed:27218149). |
Cellular Location | Nucleus. |
Thousands of laboratories across the world have published research that depended on the performance of antibodies from Abcepta to advance their research. Check out links to articles that cite our products in major peer-reviewed journals, organized by research category.
info@abcepta.com, and receive a free "I Love Antibodies" mug.
Provided below are standard protocols that you may find useful for product applications.
Background
This intronless gene belongs to the forkhead family oftranscription factors, which is characterized by a distinctforkhead domain. The protein encoded functions as a lens-specifictranscription factor and plays an important role in vertebrate lensformation. Mutations in this gene are associated with anteriorsegment mesenchymal dysgenesis and congenital primary aphakia.
References
Reis, L.M., et al. Am. J. Med. Genet. A 152A (3), 582-590 (2010) :Bremond-Gignac, D., et al. Mol. Vis. 16, 1705-1711 (2010) :Ali, M., et al. Mol. Vis. 16, 1162-1168 (2010) :Anjum, I., et al. Mol. Vis. 16, 549-555 (2010) :Iseri, S.U., et al. Hum. Mutat. 30(10):1378-1386(2009)
If you have used an Abcepta product and would like to share how it has performed, please click on the "Submit Review" button and provide the requested information. Our staff will examine and post your review and contact you if needed.
If you have any additional inquiries please email technical services at tech@abcepta.com.