SLC4A11 Produits
(Solute Carrier Family 4, Sodium Borate Transporter, Member 11 (SLC4A11))
Catégories
This gene encodes a voltage-regulated, electrogenic sodium-coupled borate cotransporter that is essential for borate homeostasis, cell growth and cell proliferation. Mutations in this gene have been associated with a number of endothelial corneal dystrophies including recessive corneal endothelial dystrophy 2, corneal dystrophy and perceptive deafness, and Fuchs endothelial corneal dystrophy. Multiple transcript variants encoding different isoforms have been described. [provided by RefSeq, Mar 2010].
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Catégories SLC4A11 en vedette
SLC4A11 Anticorps
High quality antibodies with extensive validation data.
SLC4A11 Protéines
Proteins for various applications incl. WB, ELISA, IF etc.
SLC4A11 recommandé Anticorps
Produit
Reactivity
Application
Validations
N° du produit
Quantité
Fiche technique
Reactivity
Human
Application
WB, ELISA
Validations
- (2)
N° du produit
ABIN7186031
Quantité
100 μg
Fiche technique
Fiche technique
Reactivity
Human, Mouse
Application
WB, ELISA, ICC, IF
Validations
- (2)
N° du produit
ABIN6258559
Quantité
100 μL
Fiche technique
Fiche technique
Reactivity
Human
Application
WB, ELISA, IHC
Validations
- (2)
N° du produit
ABIN571063
Quantité
100 μg
Fiche technique
Fiche technique
SLC4A11 recommandé Protéines
Produit
Reactivity
Source
Validations
N° du produit
Quantité
Fiche technique
Reactivity
Mouse
Source
Tobacco (Nicotiana tabacum)
Validations
N° du produit
ABIN3130770
Quantité
1 mg
Fiche technique
Fiche technique
Dernières publications sur nos produits SLC4A11
: "SLC4A11 mutations in Fuchs endothelial corneal dystrophy." dans: Human molecular genetics, Vol. 17, Issue 5, pp. 656-66, (2008) (PubMed).: "Identification of mutations in the SLC4A11 gene in patients with recessive congenital hereditary endothelial dystrophy." dans: Archives of ophthalmology (Chicago, Ill. : 1960), Vol. 126, Issue 5, pp. 700-8, (2008) (PubMed).
: "Autosomal recessive corneal endothelial dystrophy (CHED2) is associated with mutations in SLC4A11." dans: Journal of medical genetics, Vol. 44, Issue 1, pp. 64-8, (2007) (PubMed).
: "Borate transporter SLC4A11 mutations cause both Harboyan syndrome and non-syndromic corneal endothelial dystrophy." dans: Journal of medical genetics, Vol. 44, Issue 5, pp. 322-6, (2007) (PubMed).
: "Mutations in sodium-borate cotransporter SLC4A11 cause recessive congenital hereditary endothelial dystrophy (CHED2)." dans: Nature genetics, Vol. 38, Issue 7, pp. 755-7, (2006) (PubMed).
: "NaBC1 is a ubiquitous electrogenic Na+ -coupled borate transporter essential for cellular boron homeostasis and cell growth and proliferation." dans: Molecular cell, Vol. 16, Issue 3, pp. 331-41, (2004) (PubMed).
: "Human BTR1, a new bicarbonate transporter superfamily member and human AE4 from kidney." dans: Biochemical and biophysical research communications, Vol. 282, Issue 5, pp. 1103-9, (2001) (PubMed).
Synonymes et noms alternatifs relatifs à SLC4A11
solute carrier family 4 member 11 (Slc4a11), solute carrier family 4 member 11 (SLC4A11), solute carrier family 4 member 11 L homeolog (slc4a11.L), solute carrier family 4 member 11 (slc4a11), solute carrier family 4, sodium borate transporter, member 11 (slc4a11), solute carrier family 4, sodium bicarbonate transporter-like, member 11 (Slc4a11), AI503023, BTR1, CDPD1, CHED2, dJ794I6.2, NaBC1, NABC1, si:dkey-12j14.4Protein level used designations for SLC4A11
- sodium bicarbonate transporter-like protein 11
- solute carrier family 4, sodium bicarbonate transporter-like, member 11
- solute carrier family 4, sodium borate transporter, member 11
- sodium-coupled borate transporter
- sodium bicarbonate transporter-like protein 11-like
- solute carrier family 4 member 11
- Sodium borate cotransporter 1
- Solute carrier family 4 member 11
- bicarbonate transporter-related protein 1
- bicarbonate transporter related protein 1
- sodium-coupled borate cotransporter 1
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