SLC26A4 抗体
(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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16 results :
SLC26A4
适用: 人
ELISA, WB, IHC, IF
宿主: 兔
Polyclonal
unconjugated
SLC26A4
适用: 人
ELISA, WB
宿主: 小鼠
Polyclonal
unconjugated
1 image
2 references
SLC26A4
适用: 人, 大鼠, 小鼠, Cow, 犬, 豚鼠, 马, 兔
WB, IHC
宿主: 兔
Polyclonal
unconjugated
SLC26A4
适用: 人, Pig
ELISA, WB, IHC (p), FACS, IF (p)
宿主: 兔
Polyclonal
unconjugated
1 image
Latest Publications for our SLC26A4 抗体
: ""Reversed polarization" of Na/K-ATPase-a sign of inverted transport in the human endolymphatic sac: a super-resolution structured illumination microscopy (SR-SIM) study." in: Cell and tissue research, (2019) (PubMed).: "Pendrin, an anion exchanger on lung epithelial cells, could be a novel target for lipopolysaccharide-induced acute lung injury mice." in: American journal of translational research, Vol. 8, Issue 2, pp. 981-92, (2016) (PubMed).
: "Developmental expression of solute carrier family 26A member 4 (SLC26A4/pendrin) during amelogenesis in developing rodent teeth." in: European journal of oral sciences, Vol. 119 Suppl 1, pp. 185-92, (2012) (PubMed).
: "Novel role for pendrin in orchestrating bicarbonate secretion in cystic fibrosis transmembrane conductance regulator (CFTR)-expressing airway serous cells." in: The Journal of biological chemistry, Vol. 286, Issue 47, pp. 41069-82, (2011) (PubMed).
Aliases for SLC26A4 抗体
solute carrier family 26 member 4 (SLC26A4) 抗体solute carrier family 26 member 4 (Slc26a4) 抗体
solute carrier family 26, member 4 (Slc26a4) 抗体
DFNB4 抗体
EVA 抗体
Pds 抗体
PDS 抗体
pendrin 抗体
TDH2B 抗体
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