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LearnABIN967035
antibody from antibodies-online
Targeting: SLC4A11
BTR1, CDPD1, CHED2, dJ794I6.2, FECD4, NaBC1
ImmunohistochemistryAntibody data
- Antibody Data
- Antigen structure
- References [6]
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- Product number
- ABIN967035 - Provider product page
- Provider
- antibodies-online
- Product name
- anti-Solute Carrier Family 4, Sodium Borate Transporter, Member 11 (SLC4A11) (C-Term) antibody
- Antibody type
- Polyclonal
- Antigen
- Polyclonal antibody produced in rabbits immunizing with a synthetic peptide corresponding to C-terminal residues of human SLC4A11 (Sodium bicarbonate transporter-like protein 11)
- Reactivity
- Human, Mouse
- Host
- Rabbit
- Epitope
- C-Term
- Vial size
- 0.1 mg
Submitted references SLC4A11 mutations in Fuchs endothelial corneal dystrophy.
Borate transporter SLC4A11 mutations cause both Harboyan syndrome and non-syndromic corneal endothelial dystrophy.
Autosomal recessive corneal endothelial dystrophy (CHED2) is associated with mutations in SLC4A11.
Mutations in sodium-borate cotransporter SLC4A11 cause recessive congenital hereditary endothelial dystrophy (CHED2).
NaBC1 is a ubiquitous electrogenic Na+ -coupled borate transporter essential for cellular boron homeostasis and cell growth and proliferation.
Human BTR1, a new bicarbonate transporter superfamily member and human AE4 from kidney.
Vithana EN, Morgan PE, Ramprasad V, Tan DT, Yong VH, Venkataraman D, Venkatraman A, Yam GH, Nagasamy S, Law RW, Rajagopal R, Pang CP, Kumaramanickevel G, Casey JR, Aung T
Human molecular genetics 2008 Mar 1;17(5):656-66
Human molecular genetics 2008 Mar 1;17(5):656-66
Borate transporter SLC4A11 mutations cause both Harboyan syndrome and non-syndromic corneal endothelial dystrophy.
Desir J, Moya G, Reish O, Van Regemorter N, Deconinck H, David KL, Meire FM, Abramowicz MJ
Journal of medical genetics 2007 May;44(5):322-6
Journal of medical genetics 2007 May;44(5):322-6
Autosomal recessive corneal endothelial dystrophy (CHED2) is associated with mutations in SLC4A11.
Jiao X, Sultana A, Garg P, Ramamurthy B, Vemuganti GK, Gangopadhyay N, Hejtmancik JF, Kannabiran C
Journal of medical genetics 2007 Jan;44(1):64-8
Journal of medical genetics 2007 Jan;44(1):64-8
Mutations in sodium-borate cotransporter SLC4A11 cause recessive congenital hereditary endothelial dystrophy (CHED2).
Vithana EN, Morgan P, Sundaresan P, Ebenezer ND, Tan DT, Mohamed MD, Anand S, Khine KO, Venkataraman D, Yong VH, Salto-Tellez M, Venkatraman A, Guo K, Hemadevi B, Srinivasan M, Prajna V, Khine M, Casey JR, Inglehearn CF, Aung T
Nature genetics 2006 Jul;38(7):755-7
Nature genetics 2006 Jul;38(7):755-7
NaBC1 is a ubiquitous electrogenic Na+ -coupled borate transporter essential for cellular boron homeostasis and cell growth and proliferation.
Park M, Li Q, Shcheynikov N, Zeng W, Muallem S
Molecular cell 2004 Nov 5;16(3):331-41
Molecular cell 2004 Nov 5;16(3):331-41
Human BTR1, a new bicarbonate transporter superfamily member and human AE4 from kidney.
Parker MD, Ourmozdi EP, Tanner MJ
Biochemical and biophysical research communications 2001 Apr 20;282(5):1103-9
Biochemical and biophysical research communications 2001 Apr 20;282(5):1103-9
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