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PKD2 / Polycystin 2

polycystic kidney disease 2 (autosomal dominant)

Functions as a calcium permeable cation channel involved in fluid-flow mechanosensation by the primary cilium in renal epithelium. PKD1 and PKD2 may function through a common signaling pathway that is necessary for normal tubulogenesis. Acts as a regulator of cilium length, together with PKD1. The dynamic control of cilium length is essential in the regulation of mechanotransductive signaling. The cilium length response creates a negative feedback loop whereby fluid shear-mediated deflection of the primary cilium, which decreases intracellular cAMP, leads to cilium shortening and thus decreases flow-induced signaling. Also involved in left/right axis specification downstream of nodal flow: forms a complex with PKD2 in cilia to facilitate flow detection in left/right patterning.

Gene Name: polycystic kidney disease 2 (autosomal dominant)
Family/Subfamily: Ion Channel , Calcium channel - TRP
Synonyms: PKD2, APKD2, Pc-2, Polycystic kidney disease 2, Polycystwin, PC2, PKD4, Polycystin-2, R48321, TRPP2
Target Sequences: NM_000297 NP_000288.1 Q13563

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Proteins (1)
Recombinant (1)
PKD2 / Polycystin 2 (1)
No (1)
GST, N-terminus (1)
Human (1)
Wheat Germ Extract (1)
PKD2 / Polycystin 2 Protein - 12.5% SDS-PAGE Stained with Coomassie Blue.
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Wheat Germ Extract
GST, N-terminus
10 µg/$479; 25 µg/$670
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PLEASE NOTE

For RESEARCH USE ONLY. Intended for use by laboratory professionals. Not intended for human diagnostic or therapeutic purposes.

The data on this page has been compiled from LifeSpan internal sources, the National Center for Biotechnology Information (NCBI), and The Universal Protein Resource (UniProt).