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AQP2 encodes a water channel protein located in the kidney collecting tubule. Additionally we are shipping AQP2 Kits (49) and AQP2 Proteins (7) and many more products for this protein.
Showing 10 out of 165 products:
Cow (Bovine) Polyclonal AQP2 Primary Antibody for IHC (fro), WB - ABIN784597
Hoffert, Fenton, Moeller, Simons, Tchapyjnikov, McDill, Yu, Pisitkun, Chen, Knepper: Vasopressin-stimulated increase in phosphorylation at Ser269 potentiates plasma membrane retention of aquaporin-2. in The Journal of biological chemistry 2008
Show all 6 references for ABIN784597
Cow (Bovine) Polyclonal AQP2 Primary Antibody for IHC (fro), WB - ABIN784596
Fenton, Moeller, Hoffert, Yu, Nielsen, Knepper: Acute regulation of aquaporin-2 phosphorylation at Ser-264 by vasopressin. in Proceedings of the National Academy of Sciences of the United States of America 2008
Show all 6 references for ABIN784596
Cow (Bovine) Polyclonal AQP2 Primary Antibody for IHC (fro), WB - ABIN372590
van Balkom, Savelkoul, Markovich, Hofman, Nielsen, van der Sluijs, Deen: The role of putative phosphorylation sites in the targeting and shuttling of the aquaporin-2 water channel. in The Journal of biological chemistry 2002
Show all 6 references for ABIN372590
Human Polyclonal AQP2 Primary Antibody for ICC, IF - ABIN2486378
Gonen, Walz: The structure of aquaporins. in Quarterly reviews of biophysics 2006
Show all 2 references for ABIN2486378
Human Polyclonal AQP2 Primary Antibody for ICC, IF - ABIN2486375
Knepper: The aquaporin family of molecular water channels. in Proceedings of the National Academy of Sciences of the United States of America 1994
Show all 2 references for ABIN2486375
analysis of phosphorylation-dependent interactions of AQP2 with 14-3-3theta; and -zeta
the activation of CaSR (show CASR Antibodies) in the collecting duct prevents the cyclic AMP (show TMPRSS5 Antibodies)-dependent increase in AQP2-phosphorylation at S256 and water permeability, counteracting the short-term vasopressin (show AVP Antibodies) response.
Functional photoconvertible chimeric AQP-2 was successfully expressed in mpkCCD cells, in which forskolin induced apical trafficking and accumulation of chimeric AQP-2.
Suggest ERalpha (show ESR1 Antibodies) in mediates the inhibitory effect of estradiol on AQP2 expression in collecting ducts.
Data suggest that the ability of prostaglandin E2 receptor EP4 (show PTGER4 Antibodies) to promote aquaporin 2 (AQP2) membrane targeting and increase AQP2 abundance makes it a therapeutic target for the treatment of congenital diabetes insipidus.
Odontoblast-lineage cell line have high-cell viability under xylitol-induced hypertonic stress, which may be associated with TRPV1 (show TRPV1 Antibodies) and AQP2 expressions.
The direct renin (show REN Antibodies) inhibitor aliskiren increased water channel (show AQP4 Antibodies) AQP2 expression in obstructed kidneys of UUO mice, at least partially by preventing NLRP3 (show NLRP3 Antibodies) inflammasome activation in association with ureteral obstruction.
role for PKA signaling in both short- and long-term regulation of AQP2, characterizing a novel mouse model of diabetes insipidus
tankyrase likely to play an important role in vasopressin (show AVP Antibodies)-induced AQP2 upregulation via beta-catenin (show CTNNB1 Antibodies)-mediated transcription in the kidney collecting duct cells
Studied the effect of the total tannins extract of rhubarb on expression od aquaporin 2 and auqaporin 3 in diarrhoea mice.
report a novel mutation of the AQP2 gene and highlight an important role of genetic testing for definite diagnosis
The study demonstrated the abnormal expression pattern of AQP1 (show AQP1 Antibodies), AQP2, AQP3 (show AQP3 Antibodies), and AQP4 (show AQP4 Antibodies) in the kidney tissues of patients with nephrotic syndrome, providing a basis for an improved understanding of the role of aquaporins in the pathogenesis of this disease.
In most cases (90 %), inherited nephrogenic diabetes insipidus (show AVPR2 Antibodies) (NDI (show AVPR2 Antibodies)) is an X-linked disease, caused by mutations in the AVPR2 (show AVPR2 Antibodies) gene. * In rare occasions (10 %), it is caused by mutations in the AQP2 gene.
Partial congenital nephrogenic diabetes insipidus (show AVPR2 Antibodies) in the Swedish family is caused by an AQP2 variation that seems to disable the encoded AQP2-R254W protein to reach the subapical vesicle population as well as impairing its phosphorylation at S256
Taken together these results provide a possible molecular mechanism explaining the increased AQP2 membrane expression under RGZ treatment: in renal cells RGZ elicits Ca(2 (show CA2 Antibodies)+) transients facilitating AQP2 exposure at the apical plasma membrane
U-AQP2/P-AVP (show AVP Antibodies) is a novel predictor of response to TLV in patients with decompensated HF. AQP-defined responders may have a better prognosis on TLV treatment
In response to hypertonic saline, urinary AQP2 increased more in chronic kidney disease patients compared to controls.
results further support the view that urinary calcium can modulate the vasopressin (show AVP Antibodies)-dependent urine concentration through a down-regulation of AQP2 expression/trafficking
AQP2 is subjected to S-glutathionylation, which is modulated by reactive oxygen species production.
The genetic polymorphisms in OCT2, AQP2, AQP9 (show AQP7 Antibodies) and TMEM205 (show TMEM205 Antibodies) may contribute to chemotherapy response in lung cancer patients.
Aquaporin 2 promotes cell migration and epithelial morphogenesis.
Data provide evidence supporting the role of S256 and S269 in the maintenance of AQP2 at the cell surface.
This gene encodes a water channel protein located in the kidney collecting tubule. It belongs to the MIP/aquaporin family, some members of which are clustered together on chromosome 12q13. Mutations in this gene have been linked to autosomal dominant and recessive forms of nephrogenic diabetes insipidus.
ADH water channel
, collecting duct water channel protein
, water channel protein for renal collecting duct
, water-channel aquaporin 2