Order NO. D262518
产品描述
概述
Mutations in this gene are associated with Pendred syndrome, the most common form of syndromic deafness, an autosomal-recessive disease. It is highly homologous to the SLC26A3 gene; they have similar genomic structures and this gene is located 3' of the SLC26A3 gene. The encoded protein has homology to sulfate transporters.
应用
酶联免疫吸附测定(ELISA),免疫组织化学(IHC)
属性
保存缓冲液 |
-20°C, pH7.4 PBS, 0.05% NaN3, 40% Glycerol
|
运输条件 |
2-8°C
|
靶点 Uniprot 登记号 |
O43511
|
靶点基因 ID |
5172
|
靶点全称 |
solute carrier family 26 member 4
|
靶点别名 |
EVA; PDS; DFNB4; TDH2B
|
靶点研究领域 |
Neuroscience, Signal Transduction, Metabolism
|
亚型 |
Immunogen-specific rabbit IgG
|