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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].

20 results

SLC4A11 适用: 人 WB, ELISA 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN7186031
 
Verified SLC4A11 适用: 人 WB, ELISA, IHC 宿主: 山羊 Polyclonal unconjugated
产品编号 ABIN571063
 
SLC4A11 适用: 人, 小鼠 WB, ELISA, ICC, IF 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN6258559
 
SLC4A11 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN7270461
 
SLC4A11 适用: 人, 小鼠 IHC 宿主: 兔 Polyclonal unconjugated
Pubmed 6 references
产品编号 ABIN967035
 
SLC4A11 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN6989017
 
SLC4A11 适用: 人 WB 宿主: 兔 Polyclonal Biotin
产品编号 ABIN6982873
 
SLC4A11 适用: 人 WB 宿主: 兔 Polyclonal HRP
产品编号 ABIN6987794
 
SLC4A11 适用: 人 WB, ELISA 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN6282648
 
SLC4A11 适用: 人, 小鼠 WB, IP 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN2571683
 
SLC4A11 适用: 人 WB, ELISA 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN2885340
 
SLC4A11 适用: 人 WB, ELISA 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN1535375
 
SLC4A11 适用: 人, 小鼠, 大鼠, Cow, 犬, 小鸡, 马, 绵羊 ELISA, IHC, IF/ICC 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN5911132
 
SLC4A11 适用: 人, 小鼠 宿主: 兔 Polyclonal Alexa Fluor 680
产品编号 ABIN6909239
 
SLC4A11 适用: 人, 小鼠 宿主: 兔 Polyclonal Biotin
产品编号 ABIN6877113
 
SLC4A11 适用: 人, 小鼠 宿主: 兔 Polyclonal Alexa Fluor 555
产品编号 ABIN6893176
 
SLC4A11 适用: 人, 小鼠 宿主: 兔 Polyclonal Alexa Fluor 647
产品编号 ABIN6919790
 
SLC4A11 适用: 人, 小鼠 宿主: 兔 Polyclonal Alexa Fluor 488
产品编号 ABIN6820797
 
SLC4A11 适用: 人, 小鼠 宿主: 兔 Polyclonal Alexa Fluor 750
产品编号 ABIN6861050
 
SLC4A11 适用: 人, 小鼠 宿主: 兔 Polyclonal Alexa Fluor 594
产品编号 ABIN6836860
 
  • 类型 Primary
    • Primary
  • 应用范围
    • Western Blotting (WB)
    • ELISA
    • Immunohistochemistry (IHC)
    • Immunocytochemistry (ICC)
    • Immunofluorescence (IF)
    • Immunoprecipitation (IP)
    • Immunofluorescence (fixed cells) (IF/ICC)
  • 适用
    • Human
    • Mouse
    • Chicken
    • Cow
    • Dog
    • Horse
    • Rat
    • Sheep
  • 论文引用
  • 图像
  • Carrier free only
  • 抗体来源
    • Rabbit
    • Goat
  • 克隆形成能力
    • Polyclonal
  • 抗原表位
    • Internal Region
    • AA 61-160
    • AA 1-180
    • AA 260-340
    • AA 276-325
    • AA 291-340
    • C-Term
  • 标记
    • 非结合性
    • Biotin
    • Alexa Fluor 488
    • Alexa Fluor 555
    • Alexa Fluor 594
    • Alexa Fluor 647
    • Alexa Fluor 680
    • Alexa Fluor 750
    • HRP
  • 抗体亚型
    • IgG
  • Format
    • Liquid
  • Grade
    • Verified
  • Supplier
    • antibodies-online
    • Signalway
    • Abbexa
    • Assay Biotechnology Company, Inc.

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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