Rabbit Anti-Human PKD1L2 Polyclonal Antibody [AF594]
Autosomal dominant polycystic kidney disease (ADPKD) is characterized by slow progression of multiple renal cysts, leading to middle-age or late-stage renal insufficiency. ADPKD is mainly related to mutations in the PKD1 gene (encoding polycystin-1 or PC1). PKD1L2 (polycystic kidney disease gene 1-like 2), as a member of the polycystic protein family, can act as a component of the cation channel pore, which is very impoRoom Temperatureant in the study of ADPKD.
Product Specifications
CAS Number
9007-83-4
Shipping Conditions
Gel Pack
Storage Conditions
Store at 4°C for 12 months.
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