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- Product number
- ABIN952367 - Provider product page
- Provider
- antibodies-online
- Product name
- anti-Forkhead Box E3 (FOXE3) (AA 94-122), (Middle Region) antibody
- Antibody type
- Polyclonal
- Description
- Protein A column, followed by peptide affinity purification
- Reactivity
- Human
- Host
- Rabbit
- Epitope
- AA 94-122, Middle Region
- Vial size
- 0.4 mL
- Storage
- Store undiluted at 2-8°C for one month or (in aliquots) at -20°C for longer.
- Handling
- Avoid repeated freezing and thawing.
Submitted references FOXE3 plays a significant role in autosomal recessive microphthalmia.
A mutation in the FOXE3 gene causes congenital primary aphakia in an autosomal recessive consanguineous Pakistani family.
Homozygous FOXE3 mutations cause non-syndromic, bilateral, total sclerocornea, aphakia, microphthalmia and optic disc coloboma.
Identification of dominant FOXE3 and PAX6 mutations in patients with congenital cataract and aniridia.
Seeing clearly: the dominant and recessive nature of FOXE3 in eye developmental anomalies.
Reis LM, Tyler RC, Schneider A, Bardakjian T, Stoler JM, Melancon SB, Semina EV
American journal of medical genetics. Part A 2010 Mar;152A(3):582-90
American journal of medical genetics. Part A 2010 Mar;152A(3):582-90
A mutation in the FOXE3 gene causes congenital primary aphakia in an autosomal recessive consanguineous Pakistani family.
Anjum I, Eiberg H, Baig SM, Tommerup N, Hansen L
Molecular vision 2010 Mar 30;16:549-55
Molecular vision 2010 Mar 30;16:549-55
Homozygous FOXE3 mutations cause non-syndromic, bilateral, total sclerocornea, aphakia, microphthalmia and optic disc coloboma.
Ali M, Buentello-Volante B, McKibbin M, Rocha-Medina JA, Fernandez-Fuentes N, Koga-Nakamura W, Ashiq A, Khan K, Booth AP, Williams G, Raashid Y, Jafri H, Rice A, Inglehearn CF, Zenteno JC
Molecular vision 2010 Jun 23;16:1162-8
Molecular vision 2010 Jun 23;16:1162-8
Identification of dominant FOXE3 and PAX6 mutations in patients with congenital cataract and aniridia.
Brémond-Gignac D, Bitoun P, Reis LM, Copin H, Murray JC, Semina EV
Molecular vision 2010 Aug 22;16:1705-11
Molecular vision 2010 Aug 22;16:1705-11
Seeing clearly: the dominant and recessive nature of FOXE3 in eye developmental anomalies.
Iseri SU, Osborne RJ, Farrall M, Wyatt AW, Mirza G, Nürnberg G, Kluck C, Herbert H, Martin A, Hussain MS, Collin JR, Lathrop M, Nürnberg P, Ragoussis J, Ragge NK
Human mutation 2009 Oct;30(10):1378-86
Human mutation 2009 Oct;30(10):1378-86
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