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anti-Mouse (Murine) SLC22A17 Antibodies:
anti-Human SLC22A17 Antibodies:
anti-Rat (Rattus) SLC22A17 Antibodies:
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Human Polyclonal SLC22A17 Primary Antibody for WB - ABIN541360
Koepsell, Endou: The SLC22 drug transporter family. in Pflügers Archiv : European journal of physiology 2004
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Human Polyclonal SLC22A17 Primary Antibody for ELISA, WB - ABIN1003142
Rizwan, Burckhardt: Organic anion transporters of the SLC22 family: biopharmaceutical, physiological, and pathological roles. in Pharmaceutical research 2007
Show all 4 Pubmed References
Human Polyclonal SLC22A17 Primary Antibody for IF (p), IHC (p) - ABIN668691
Wu, Du, Lok, Lo, Xing: Lipocalin-2 enhances angiogenesis in rat brain endothelial cells via reactive oxygen species and iron-dependent mechanisms. in Journal of neurochemistry 2015
Cow (Bovine) Polyclonal SLC22A17 Primary Antibody for ELISA - ABIN451702
Devireddy, Gazin, Zhu, Green: A cell-surface receptor for lipocalin 24p3 selectively mediates apoptosis and iron uptake. in Cell 2005
Cow (Bovine) Polyclonal SLC22A17 Primary Antibody for WB - ABIN2781648
Fang, Xu, Lu, Liao, Cai, Shen, Li: A novel alternative spliced variant of neutrophil gelatinase-associated lipocalin receptor in oesophageal carcinoma cells. in The Biochemical journal 2007
Show all 2 Pubmed References
Human Polyclonal SLC22A17 Primary Antibody for IHC (p) - ABIN5588123
Cabedo Martinez, Weinhäupl, Lee, Wolff, Storch, Żerko, Konrat, Koźmiński, Breuker, Thévenod, Coudevylle et al.: Biochemical and Structural Characterization of the Interaction between the Siderocalin NGAL/LCN2 (Neutrophil Gelatinase-associated Lipocalin/Lipocalin 2) and the N-terminal Domain of Its Endocytic ... in The Journal of biological chemistry 2016
24p3R binds proteins filtered by the kidney with high affinity and may contribute to receptor-mediated endocy of proteins
cloning of the lipocalin 24p3 receptor (24p3R). Ectopic 24p3R expression confers on cells the ability to undergo either iron uptake or apoptosis, dependent upon the iron content of the ligand.
Results showed the expression levels of NGAL and NGALR significantly downregulated in clear cell renal cell carcinoma samples.
Biochemical and Structural Characterization of the Interaction between the Siderocalin NGAL/LCN2 (Neutrophil Gelatinase-associated Lipocalin/Lipocalin 2) and the N-terminal Domain of Its Endocytic Receptor SLC22A17.
Two novel variants in SLC22A17 and SLC22A7 were significantly associated with anthracycline-induced cardiotoxicity.
Lipocalin 2 might restore the health and regeneration potential of MSCs by decreasing senescence
No significant difference was found in the expressions of NGALR mRNA in placenta among moderate preeclampsia group, severe preeclampsia group and control group.
NGAL and NGALR expression might be served as novel prognostic factors and potential therapeutic targets in Hepatocellular carcinoma.
This study suggested that NGAL and NGALR expression are frequently up-regulated in gliomas, and are closely associated with poor clinical outcome.
These results suggested that SLC22A17, in cooperation with LCN2, to be involved in the acquisition of aggressive behavior among endometrial carcinoma cells.
Neutrophil gelatinase-associated lipocalin receptor (NGALR) is differentially expressed in human glomerular disease and is significantly up-regulated by Il-1beta in HMC via MAPK/ERK activation.
NGALR hypomethylation contributes to its expression in esophageal carcinomas and that this overexpression may play a role in the pathogenesis of esophageal carcinomas.
may act as a brain-specific organic ion transporter
solute carrier family 22, member 17
, solute carrier family 22 (organic cation transporter), member 17
, 24p3 receptor
, brain-type organic cation transporter
, lipocalin-2 receptor
, organic cation transporter BOCT
, solute carrier family 22 member 17
, NGAL receptor
, neutrophil gelatinase-associated lipocalin receptor
, potent brain type organic ion transporter
, brain-specific organic ion transporter