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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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| Invitrogen Antibodies | PA5-98158 |
Polyclonal |
WB
EL
ICC
IHC
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| Cusabio Biotech Co., Ltd | CSB-PA021527LA01HU |
Polyclonal |
WB
EL
ICC
IHC
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| antibodies-online | ABIN502165 |
1 references | Polyclonal |
WB
IHC
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| Bioss | bs-6787R |
1 references | Polyclonal |
WB
ICC
IHC
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