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.
Swiss Prot
O43511
Gene ID
5172
亚细胞定位
Cell membrane Secreted
宿主
Rabbit
克隆类型
Polyclonal Antibody
亚型
IgG
蛋白分子量
86kDa
稀释比例
WB 1:500-2000. IHC 1:20-50.
免疫原
A synthetic peptide of human SLC26A4
Public Immunogen Range
A synthetic peptide of human SLC26A4
纯化方法
Affinity purification
储存液
Buffer: PBS with 0.03% Proclin300, 50% glycerol, pH7.3.
保存
Store at -20°C. Avoid freeze / thaw cycles.
性状
液体
交叉反应
Human
应用
WB IHC
规格
50ul 100ul
单位
支
备注:
以上数据均来自公开文献, Solarbio暂未进行独立验证, 仅供参考。
These protocols are for reference only. Solarbio does not independently validate these methods.
温馨提示:
使用前请离心。如有问题请及时联系我们。
Quick spin before use. If you have any questions, please contact us.
实验图
Western blot analysis with SLC26A4 antibody at dilution at 1:1000
Immunohistochemistry of paraffin-embedded Liver cancer(hu) using SLC26A4 at dilution of 1:25 (x100 lens,x200 lens).