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SLC4A11 抗体

(Solute Carrier Family 4, Sodium Borate Transporter, Member 11 (SLC4A11))
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].
SLC4A11 抗体  (Internal Region) SLC4A11 抗体  (Internal Region) SLC4A11 抗体 (Internal Region) (ABIN7186031)

SLC4A11 适用: 人 WB, ELISA 宿主: 兔 Polyclonal unconjugated

SLC4A11 抗体  (Internal Region) SLC4A11 抗体  (Internal Region) SLC4A11 抗体 (Internal Region) (ABIN6258559)

SLC4A11 适用: 人, 小鼠 WB, ELISA, ICC, IF 宿主: 兔 Polyclonal unconjugated

SLC4A11 抗体  (Internal Region) SLC4A11 抗体  (Internal Region) SLC4A11 抗体 (Internal Region) (ABIN571063)

Verified SLC4A11 适用: 人 WB, ELISA, IHC 宿主: 山羊 Polyclonal unconjugated

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Find SLC4A11 抗体 for a variety of species such as anti-Human SLC4A11, anti-Mouse SLC4A11, anti-Chicken SLC4A11. The species listed below are among those available. Click on a link to go to the corresponding products.

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SLC4A11 抗体 by 标记

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Popular 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
Reactivity Human
Application IHC (p)
Validations
  • (1)
Cat. No. ABIN5588250
Quantity 100 μL
Datasheet Datasheet
Reactivity Human
Application WB
Validations
  • (1)
Cat. No. ABIN7270461
Quantity 100 μL
Datasheet Datasheet
Reactivity Human, Mouse
Application IHC
Validations
  • (6)
Cat. No. ABIN967035
Quantity 0.1 mg
Datasheet Datasheet
Reactivity Human
Application WB
Validations
Cat. No. ABIN6989017
Quantity 100 μL
Datasheet Datasheet
Reactivity Human
Application WB
Validations
Cat. No. ABIN6982873
Quantity 100 μL
Datasheet Datasheet
Reactivity Human
Application WB
Validations
Cat. No. ABIN6987794
Quantity 100 μL
Datasheet Datasheet
Reactivity Human
Application WB, ELISA
Validations
Cat. No. ABIN6282648
Quantity 50 μL
Datasheet Datasheet
Reactivity Human, Mouse
Application WB, IP
Validations
Cat. No. ABIN2571683
Quantity 100 μL
Datasheet Datasheet
Reactivity Human
Application WB, ELISA
Validations
Cat. No. ABIN2885340
Quantity 100 μL
Datasheet Datasheet
Reactivity Human, Mouse
Application WB, ELISA
Validations
Cat. No. ABIN5588251
Quantity 100 μg
Datasheet Datasheet
Reactivity Human
Application WB, ELISA
Validations
  • (1)
Cat. No. ABIN1535375
Quantity 100 μg
Datasheet Datasheet
Reactivity Chicken, Cow, Dog, Horse, Human, Mouse, Rat, Sheep
Application ELISA, IHC, IF/ICC
Validations
  • (1)
Cat. No. ABIN5911132
Quantity 100 μL
Datasheet Datasheet

Latest Publications for our SLC4A11 抗体

Vithana, Morgan, Ramprasad, Tan, Yong, Venkataraman, Venkatraman, Yam, Nagasamy, Law, Rajagopal, Pang, Kumaramanickevel, Casey, Aung: "SLC4A11 mutations in Fuchs endothelial corneal dystrophy." in: Human molecular genetics, Vol. 17, Issue 5, pp. 656-66, (2008) (PubMed).

Hemadevi, Veitia, Srinivasan, Arunkumar, Prajna, Lesaffre, Sundaresan: "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).

Jiao, Sultana, Garg, Ramamurthy, Vemuganti, Gangopadhyay, Hejtmancik, Kannabiran: "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).

Desir, Moya, Reish, Van Regemorter, Deconinck, David, Meire, Abramowicz: "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).

Vithana, Morgan, Sundaresan, Ebenezer, Tan, Mohamed, Anand, Khine, Venkataraman, Yong, Salto-Tellez, Venkatraman, Guo, Hemadevi, Srinivasan, Prajna, Khine, Casey, Inglehearn, Aung: "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).

Park, Li, Shcheynikov, Zeng, Muallem: "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).

Parker, Ourmozdi, Tanner: "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).

Aliases for SLC4A11 抗体

solute carrier family 4 member 11 (Slc4a11) 抗体
solute carrier family 4 member 11 (SLC4A11) 抗体
solute carrier family 4 member 11 L homeolog (slc4a11.L) 抗体
solute carrier family 4 member 11 (slc4a11) 抗体
solute carrier family 4, sodium borate transporter, member 11 (slc4a11) 抗体
solute carrier family 4, sodium bicarbonate transporter-like, member 11 (Slc4a11) 抗体
AI503023 抗体
BTR1 抗体
CDPD1 抗体
CHED2 抗体
dJ794I6.2 抗体
NaBC1 抗体
NABC1 抗体
si:dkey-12j14.4 抗体
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