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sodium dependent nucleoside transporter. Additionally we are shipping and and many more products for this protein.
Brazilian Amerindian ancestry compared to Asian, European, and African Genomes.SNPs within or proximal to CIITA (show CIITA ELISA Kits) (rs6498115), SMC6 (rs1834619), and KLHL29 (rs2288697) were most differentiated in the Amerindian-specific branch. SNPs in ADAMTS9 (show ADAMTS9 ELISA Kits) (rs7631391), DOCK2 (show DOCK2 ELISA Kits) (rs77594147), SLC28A1 (rs28649017), ARHGAP5 (show ARHGAP5 ELISA Kits) (rs7151991), and CIITA (show CIITA ELISA Kits) (rs45601437) in the Asian comparison.
results that validate the newly developed structural homology model of CNT membrane architecture for human CNTs, revealed extended conformationally mobile regions within transport-domain TMs (show TYMS ELISA Kits), identified pore-lining residues of functional importance, and provided evidence of an emerging novel elevator-type mechanism of transporter function.
ErbB2 modulates gemcitabine and irinotecan/SN-38 chemoresistance of human pancreatic cancer cells via hCNT1 transporter and multidrug-resistance associated protein MRP-2.
hCNT1 is a putative determinant for nucleoside analog chemoresistance in ovarian cancer.
Human CNT1 fits the profile of a transceptor in a substrate translocation-independent manner and is likely to be relevant to tumor biology.
MUC4 (show MUC4 ELISA Kits) and hCNT1 as potential targets to ameliorate the response of pancreatic tumors to gemcitabine treatment.
CNT1-mediated gemcitabine uptake shows a higher correlation with the CNT1 expression level than does ENT1 (show SLC29A1 ELISA Kits)-mediated uptake with ENT1 (show SLC29A1 ELISA Kits) expression.
Site-directed mutagenesis analysis reveals that only one sodium binding site is affected by a mutation; lack of serine546 residue is responsible for apparent loss of CNT1 function.
our findings identify hCNT1 as a potential candidate to render drug-resistant pancreatic cancer cells amenable to chemotherapy.
Two pyrimidine nucleoside analogs were potent inhibitors of CNT1, with negligible transportability and little apparent cytotoxicity, suggesting that they may have utility as cytoprotective agents.
sodium dependent nucleoside transporter
, Na(+)/nucleoside cotransporter 1
, concentrative nucleoside transporter 1
, sodium-coupled nucleoside transporter 1
, sodium/nucleoside cotransporter 1
, solute carrier family 28 member 1
, solute carrier family 28 (sodium-coupled nucleoside transporter), member 1
, solute carrier family 28, member 1