SLC26A4 ELISA试剂盒
(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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4 results :
SLC26A4
适用: 人
Colorimetric
Sandwich ELISA
0.781 ng/mL - 50 ng/mL
Plasma, Serum, Tissue Homogenate
1 image
SLC26A4
适用: 大鼠
Colorimetric
Sandwich ELISA
0.313 ng/mL - 20 ng/mL
Plasma, Serum, Tissue Homogenate
1 image
SLC26A4
适用: 人
Colorimetric
Sandwich ELISA
0.31 ng/mL - 20 ng/mL
Cell Lysate, Tissue Homogenate
1 image
Aliases for SLC26A4 ELISA试剂盒
solute carrier family 26 member 4 (SLC26A4) ELISA试剂盒solute carrier family 26 member 4 (Slc26a4) ELISA试剂盒
solute carrier family 26, member 4 (Slc26a4) ELISA试剂盒
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