SLC4A11 Produkte
(Solute Carrier Family 4, Sodium Borate Transporter, Member 11 (SLC4A11))
Kategorien
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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Ausgewählte SLC4A11 Kategorien
SLC4A11 Antikörper
High quality antibodies with extensive validation data.
SLC4A11 Proteine
Proteins for various applications incl. WB, ELISA, IF etc.
Empfohlene SLC4A11 Antikörper
Produkt
Reaktivität
Applikation
Validierungen
Kat. Nr.
Menge
Datenblatt
Reaktivität
Human
Applikation
WB, ELISA
Validierungen
- (2)
Kat. Nr.
ABIN7186031
Menge
100 μg
Datenblatt
Datenblatt
Reaktivität
Human, Mouse
Applikation
WB, ELISA, ICC, IF
Validierungen
- (2)
Kat. Nr.
ABIN6258559
Menge
100 μL
Datenblatt
Datenblatt
Reaktivität
Human
Applikation
WB, ELISA, IHC
Validierungen
- (2)
Kat. Nr.
ABIN571063
Menge
100 μg
Datenblatt
Datenblatt
Empfohlene SLC4A11 Proteine
Produkt
Reaktivität
Source
Validierungen
Kat. Nr.
Menge
Datenblatt
Reaktivität
Human
Source
Insect Cells
Validierungen
Kat. Nr.
ABIN3116626
Menge
1 mg
Datenblatt
Datenblatt
Reaktivität
Mouse
Source
Tobacco (Nicotiana tabacum)
Validierungen
Kat. Nr.
ABIN3130770
Menge
1 mg
Datenblatt
Datenblatt
Neueste Publikationen zu unseren SLC4A11 Produkten
: "SLC4A11 mutations in Fuchs endothelial corneal dystrophy." in: 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." in: 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." in: 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." in: 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)." in: 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." in: Molecular cell, Vol. 16, Issue 3, pp. 331-41, (2004) (PubMed).
: "Human BTR1, a new bicarbonate transporter superfamily member and human AE4 from kidney." in: Biochemical and biophysical research communications, Vol. 282, Issue 5, pp. 1103-9, (2001) (PubMed).
Synonyme und alternative Namen zu 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-12j14.4Bezeichner auf Proteinebene für 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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