PKD-2 antibodies are critical for:
Western Blot (WB): Detects endogenous PKD2 at ~110 kDa in human, mouse, and rat tissues .
Immunohistochemistry (IHC): Localizes PKD2 in renal tubules, cilia, and vascular endothelia .
Flow Cytometry: Quantifies PKD2 expression in fixed/permeabilized cells .
Functional Studies: Validates PKD2’s role in calcium signaling, cystogenesis, and mitochondrial bioenergetics .
Cyst Formation: PKD2 mutations disrupt polycystin-2’s interaction with polycystin-1, leading to aberrant cell proliferation and renal cyst growth .
Calcium Signaling: PKD2 regulates intracellular Ca²⁺ levels via ciliary and endoplasmic reticulum (ER) channels, impacting mitochondrial metabolism .
miRNA Regulation: PKD2 mRNA contains miR-17 binding sites; deletion of these motifs rescues mitochondrial dysfunction in PKD1-mutant models .
Structural Interactions: PKD2 forms homodimers and heterodimers with PKD1, stabilizing both proteins and enabling coordinated signaling .
Ion Channel Activity: Reconstituted PKD2 in lipid bilayers shows Ca²⁺-permeable channel activity inhibited by La³⁺, Gd³⁺, and amiloride .
Subcellular Localization: PKD2 localizes to primary cilia, ER, and plasma membrane, with roles in mechanosensation and left-right asymmetry .
Validation: Antibody specificity confirmed via knockout controls and peptide blocking .
Challenges: Cross-reactivity with non-target proteins (e.g., PKD1) varies by clone; Cell Signaling’s #8188 shows no cross-reactivity .