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member of the major intrinsic protein family. Additionally we are shipping and many more products for this protein.
Showing 10 out of 30 products:
Mouse (Murine) Polyclonal AQP11 Primary Antibody for EIA, WB - ABIN492779
Wang, Chen, Beall, Zhou, Ross: Expression of aquaporin 9 in human chorioamniotic membranes and placenta. in American journal of obstetrics and gynecology 2004
Show all 5 references for ABIN492779
Human Polyclonal AQP11 Primary Antibody for FACS, IHC (p) - ABIN651990
Morishita, Matsuzaki, Hara-chikuma, Andoo, Shimono, Matsuki, Kobayashi, Ikeda, Yamamoto, Verkman, Kusano, Ookawara, Takata, Sasaki, Ishibashi: Disruption of aquaporin-11 produces polycystic kidneys following vacuolization of the proximal tubule. in Molecular and cellular biology 2005
Human Polyclonal AQP11 Primary Antibody for ICC, IF - ABIN4281300
Takumida, Takumida, Kakigi, Egami, Nishioka, Anniko: Localization of aquaporins in the mouse vestibular end organs. in Acta oto-laryngologica 2013
Data suggest that boar spermatozoa express AQP11 and AQP7 (show AQP7 Antibodies); amounts of AQP11 (but not those of AQP7 (show AQP7 Antibodies)) are correlated with sperm motility, membrane integrity, and membrane fluidity. These studies were conducted in Spain in Pietrain boars.
The results suggest the involvement of autophagy in the development and maintenance of kidney cysts in AQP11(-/-) mice.
AQP11 was expressed mainly in the pia (show RICTOR Antibodies) matter with limited expression in the capillary at early postnatal stages at P1~P14 (show PCOLCE Antibodies).
impaired glycosylation processing and aberrant membrane trafficking of PC-1 (show PCSK1 Antibodies) in AQP11(-/-) mice could be a key mechanism of cystogenesis in AQP11(-/-) mice
Our results indicate an important role for AQP11 to prevent glucose-induced oxidative stress in proximal tubules.
deletion of AQP11 results in disrupted rough endoplasmic reticulum homeostasis and increased sensitivity to rough endoplasmic reticulum injury upon metabolic challenge with amino acid
mouse aquaporin 11 could be involved in slow but constant water movement across the membrane
Immunohistochemistry of mouse testis across development pinpointed first appearance of AQP11 coinciding with late stage elongated spermatids. cDNA analysis yielded conformation of sequence. Western blotting revealed additional forms.
AQP11 is essential for the proximal tubular function
These results provide new insights into the physiological roles of AQP11.
mutation causing single amino acid substitution in aquaporin 11 causes renal failure in sudden juvenile death syndrome mutant mice
Aquaporins AQP3 (show AQP3 Antibodies), -7, -8, and -11 proteins were found in sperm cells and localized in the head (AQP7 (show AQP7 Antibodies)), in the middle piece (AQP8 (show AQP8 Antibodies)) and in the tail (AQP3 (show AQP3 Antibodies) and -11) in both the plasma membrane and in intracellular structures.
Built accurate 3D-models for AQP11 and AQP12 (show AQP12A Antibodies) and comprehensively compared their sequence and structure to other known aquaporins.
the corresponding NPC (show NPC1 Antibodies) motif of AQP11 is essential for full expression of molecular function.
member of the major intrinsic protein family
, CG12251 gene product