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NaDC3-related immunostaining was detected in the basolateral membrane of proximal tubules and in the basolateral membrane and/or luminal membrane of principal cells in connecting segments and collecting ducts
OAT1 (show KCNK3 Proteins) and NaDC3 in the basolateral membrane and OAT4 (show SLC22A9 Proteins) in the luminal membrane of proximal tubule cells are responsible for the avid renal secretion of N-carbamoylglutamate.
In a study addressing genetic, social, and environmental contributors of chronic kidney disease with tubulointerstitial damages in Sri (show SRI Proteins) Lanka, SNP rs6066043 of SLC13A3 was found attributable risk of 50%.
study concludes NaDC3 present at the basolateral membrane of proximal tubule cells mediates sodium-dependent glutathione (GSH) uptake; the kinetic data show that NaDC3 is a low-affinity GSH transporter
The data 1) reveal alpha-ketoglutarate as a common high-affinity substrate of NaDC3, OAT1 (show KCNK3 Proteins), and OAT3 (show SLC22A8 Proteins)
The results indicate that SLC13A3 is a direct downstream target of PITX2 (show PITX2 Proteins) transcriptional regulation and that levels of PITX2 (show PITX2 Proteins) and SLC13A3 modulate responses to oxidative stress in ocular cells.
NaDC3 promotes cellular senescence probably by inhibiting NAD(+)-dependent SIRT1 (show SIRT1 Proteins).
The narrow substrate specificity prevents interaction of drugs with dicarboxylate-like structure with hNaDC-3 and ensures sufficient support of the proximal tubule cells with alpha-ketoglutarate for anion secretion via organic anion transporter 1 (show SLC22A6 Proteins) or 3.
We provide direct evidence of the localization of NaDC3 at the basolateral membrane of human renal proximal tubule cells and identify a di-hydrophobic amino acid motif VW as basolateral localization signal in the N-terminal cytoplasmic domain of NaDC3.
demonstrate the membrane translocation of 3OH-GA mediated by NaDC3 and the cis (show CISH Proteins)-inhibitory effect on OCT2 (show SLC22A2 Proteins)-mediated transport of cations
Mammalian sodium-dicarboxylate cotransporters transport succinate and other Krebs cycle intermediates. They fall into 2 categories based on their substrate affinity: low affinity and high affinity. Both the low- and high-affinity transporters play an important role in the handling of citrate by the kidneys. The protein encoded by this gene represents the high-affinity form. Alternatively spliced transcript variants encoding different isoforms have been found for this gene, although the full-length nature of some of them have not been characterized yet.
solute carrier family 13 (sodium-dependent dicarboxylate transporter), member 3
, solute carrier family 13 member 3
, Na(+)/dicarboxylate cotransporter 3
, sodium-dependent high affinity dicarboxylate transporter 3
, sodium-dependent high-affinity dicarboxylate transporter 2
, sodium-dependent high-affinity dicarboxylate transporter 3