SLC26A4 蛋白
(Solute Carrier Family 26, Member 4 (SLC26A4))
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. [provided by RefSeq, Jul 2008].
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5 results
custom-made
SLC26A4
宿主: 小鼠
宿主: Cell-free protein synthesis (CFPS)
Recombinant
approximately 70-80 % as determined by SDS PAGE, Western Blot and analytical SEC (HPLC).
WB, SDS, ELISA
custom-made
SLC26A4
宿主: 人
宿主: Cell-free protein synthesis (CFPS)
Recombinant
approximately 70-80 % as determined by SDS PAGE, Western Blot and analytical SEC (HPLC).
WB, SDS, ELISA
SLC26A4
宿主: 大鼠
宿主: 大肠杆菌（E. Coli）
Recombinant
> 90 %
WB, SDS, Imm, PC
Aliases for SLC26A4 蛋白
solute carrier family 26 member 4 (SLC26A4) 蛋白solute carrier family 26 member 4 (Slc26a4) 蛋白
solute carrier family 26, member 4 (Slc26a4) 蛋白
DFNB4 蛋白
EVA 蛋白
Pds 蛋白
PDS 蛋白
pendrin 蛋白
TDH2B 蛋白
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