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Sodium/sulfate cotransporter that mediates sulfate reabsorption in the high endothelial venules (HEV).. Additionally we are shipping and and many more products for this protein.
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Study found that despite differential expression of the two SLC13A4 transcripts, no detectable functional difference in the cellular sorting or sulfate transporting was found. However, some variants can influence both mechanism in specific cell membranes. This is like to have clinical implications based on the consequences of impaired sulfate transport during pregnancy in rodent models.
SLC13A4 and SLC26A2 were the most abundant sulfate transporter mRNAs, which localized to syncytiotrophoblast and cytotrophoblast cells, respectively.
To investigate the regulation of SLC13A4 gene expression, we analysed the transcriptional activity of the SLC13A4 5'-flanking region in the JEG-3 placental cell line using luciferase reporter assays.
Here, we characterized the functional properties of the human Na(+)-sulfate cotransporter (hNaS2), determined its tissue distribution, and identified its gene (SLC13A4) structure.
Study describes the critical requirement of placental Slc13a4 activity for normal fetal development in mice.
Tissue distribution of mNaS2 and its cDNA and gene structures.
Sodium/sulfate cotransporter that mediates sulfate reabsorption in the high endothelial venules (HEV).
Na(+)/sulfate cotransporter SUT-1
, solute carrier family 13 (sodium/sulfate symporters), member 4
, solute carrier family 13 (sodium/sulphate symporters), member 4
, solute carrier family 13 member 4
, sulphate transporter 1
, sodium sulfate cotransporter-2
, solute carrier family 13, member 4