SLC4A11 产品
(Solute Carrier Family 4, Sodium Borate Transporter, Member 11 (SLC4A11))
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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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SLC4A11 抗体
High quality antibodies with extensive validation data.
SLC4A11 蛋白
Proteins for various applications incl. WB, ELISA, IF etc.
Recommended SLC4A11 抗体
Product
Reactivity
Application
Validations
Cat. No.
Quantity
Datasheet
Reactivity
Human
Application
WB, ELISA
Validations
- (2)
Cat. No.
ABIN7186031
Quantity
100 μg
Datasheet
Datasheet
Reactivity
Human, Mouse
Application
WB, ELISA, ICC, IF
Validations
- (2)
Cat. No.
ABIN6258559
Quantity
100 μL
Datasheet
Datasheet
Reactivity
Human
Application
WB, ELISA, IHC
Validations
- (2)
Cat. No.
ABIN571063
Quantity
100 μg
Datasheet
Datasheet
Recommended SLC4A11 蛋白
Product
Reactivity
Source
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Cat. No.
Quantity
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Reactivity
Mouse
Source
Tobacco (Nicotiana tabacum)
Validations
Cat. No.
ABIN3130770
Quantity
1 mg
Datasheet
Datasheet
Latest Publications for our SLC4A11 Products
: "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).
Synonyms and alternative names related to 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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