Anti-PKD2 antibody (STJ13101577)

SPECIFICATIONS
ClonalityPolyclonal
HostRabbit
ConjugationUnconjugated
IsotypeIgG
ImmunogenA synthetic peptide from mouse PKD2 conjugated to blue carrier protein was used as the antigen.
STJ13101577-100
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General Information

Short DescriptionRabbit polyclonal anti-PKD2 for use in IHC and WB in Mouse samples. Datasheet included with dilution recommendations, and related reagents.
ApplicationsIHC/WB
HostRabbit
ReactivityMouse
NoteSTRICTLY FOR FURTHER SCIENTIFIC RESEARCH USE ONLY (RUO). MUST NOT TO BE USED IN DIAGNOSTIC OR THERAPEUTIC APPLICATIONS.

Product Properties

ClonalityPolyclonal
IsotypeIgG
ConjugationUnconjugated
PurificationIgG purified
Dilution RangeIHC, WB. A dilution of 1:1000 is recommended. The optimal dilution should be determined by the end user. Not yet tested in other applications.
FormulationLyophilised
Storage InstructionMaintain the lyophilised/reconstituted antibodies frozen at-20°C for long term storage and refrigerated at 2-8°C for a shorter term. When reconstituting, Glycerol (1:1) may be added for an additional stability. Avoid freeze and thaw cycles.

Target Information

Gene SymbolPkd2
Gene ID18764
Uniprot IDPKD2_MOUSE
ImmunogenA synthetic peptide from mouse PKD2 conjugated to blue carrier protein was used as the antigen.
SpecificitySpecific for PKD2.

Additional Info

Post Translational Modifications N-glycosylated. The four subunits in a tetramer probably differ in the extent of glycosylation.simultaneous glycosylation of all experimentally validated sites would probably create steric hindrance. Sumoylated by SUMO1.sumoylation regulates PKD2 membrane recycling and is necessary for intravascular pressure-induced arterial contractility. Phosphorylated. Phosphorylation is important for protein function.a mutant that lacks the N-terminal phosphorylation sites cannot complement a zebrafish pkd2-deficient mutant. PKD-mediated phosphorylation at the C-terminus regulates its function in the release of Ca(2+) stores from the endoplasmic reticulum. Phosphorylation at Ser-810 regulates PKD2 trafficking. Phosphorylation at Ser-72 is required for PKD2 trafficking to or retention at the lateral plasma membrane. Phosphorylation at Ser-799, Ser-810 and Ser-827 regulates PKD2 channel activity.
Function Forms a nonselective cation channel. Can function as a homotetrameric ion channel or can form heteromer with PKD1. Displays distinct function depending on its subcellular localization and regulation by its binding partners. Functions as a cation channel, with a preference for monovalent cations over divalent cations that allows K(+), Na(+) and Ca(2+) influx, with low selectivity for Ca(2+). Involved in fluid-flow mechanosensation by the primary cilium in renal epithelium. In the endoplasmic reticulum, likely functions as a K(+) channel to facilitate Ca(2+) release. The heterotetrameric PKD1/PKD2 channel has higher Ca(2+) permeability than homomeric PKD2 channel and acts as a primarily Ca(2+)-permeable channel. PKD1 and PKD2 may function through a common signaling pathway that is necessary to maintain the normal, differentiated state of renal tubule cells. Interacts with and acts as a regulator of a number of other channels, such as TRPV4, TRPC1, IP3R, RYR2, ultimately further affecting intracellular signaling, to modulate intracellular Ca(2+) signaling. Together with TRPV4, forms mechano- and thermosensitive channels in cilium. In cardiomyocytes, PKD2 modulates Ca(2+) release from stimulated RYR2 receptors through direct association. Also involved in left-right axis specification via its role in sensing nodal flow.forms a complex with PKD1L1 in cilia to facilitate flow detection in left-right patterning. Acts as a regulator of cilium length together with PKD1. Mediates systemic blood pressure and contributes to the myogenic response in cerebral arteries though vasoconstriction.
Protein Name Polycystin-2
Polycystic Kidney Disease 2 Protein Homolog
Transient Receptor Potential Cation Channel Subfamily P Member 2
Database Links Reactome: R-MMU-5620916
Cellular Localisation Cell Projection
Cilium Membrane
Multi-Pass Membrane Protein
Cell Membrane
Basolateral Cell Membrane
Cytoplasmic Vesicle Membrane
Endoplasmic Reticulum Membrane
Golgi Apparatus
Vesicle
Secreted
Extracellular Exosome
Pkd2 Localization To The Plasma And Ciliary Membranes Requires Pkd1
Pkd1:Pkd2 Interaction Is Required To Reach The Golgi Apparatus Form Endoplasmic Reticulum And Then Traffic To The Cilia
Detected On Kidney Tubule Basolateral Membranes And Basal Cytoplasmic Vesicles
Retained In The Endoplasmic Reticulum By Interaction With Pacs1 And Pacs2
Cilium Localization Requires Ganab
Detected On Migrasomes And On Extracellular Exosomes In Urine
Preferentially Localized To The Dorsal Side Of Immotile Cilia
Alternative Antibody Names Anti-Polycystin-2 antibody
Anti-Polycystic Kidney Disease 2 Protein Homolog antibody
Anti-Transient Receptor Potential Cation Channel Subfamily P Member 2 antibody
Anti-Pkd2 antibody
Anti-TRPP2 antibody

Information sourced from Uniprot.org

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