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Cell line expression
Protein structure
SLC26A4
Solute carrier family 26 member 4DFNB4, PDS
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]
Top validated antibodies |
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| Novus Biologicals |  NBP1-60106 |
3 references | Polyclonal |
WB
IHC
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| Cusabio Biotech Co., Ltd | CSB-PA021527LA01HU |
Polyclonal |
WB
EL
ICC
IHC
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| Biorbyt | orb417939 |
Polyclonal |
WB
EL
ICC
IHC
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| Invitrogen Antibodies | PA5-98158 |
Polyclonal |
WB
EL
ICC
IHC
|
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| LSBio | LS-C673140 |
Polyclonal |
WB
EL
ICC
IHC
|
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