STRUM Rabbit Polyclonal Antibody

This gene encodes a 134 kDa protein named strumpellin that is predicted to have multiple transmembrane domains and a spectrin-repeat-containing domain. This ubiquitously expressed gene has its highest expression in skeletal muscle. The protein is named for Strumpell disease; a form of hereditary spastic paraplegia (HSP). Spastic paraplegias are a diverse group of disorders in which the autosomal dominant forms are characterized by progressive| lower extremity spasticity caused by axonal degeneration in the terminal portions of the longest descending and ascending corticospinal tracts. More than 30 loci (SPG1-33) have been implicated in hereditary spastic paraplegia diseases.

The STRUM Rabbit Polyclonal Antibody is a highly reliable and efficient tool for various research applications. This antibody is specifically designed to target and detect the STRUM protein, enabling accurate analysis and investigation of its biological functions. With its exceptional sensitivity and specificity, this polyclonal antibody ensures precise and reproducible results in immunohistochemistry, western blotting, and other experimental techniques. Manufactured using advanced techniques and quality-controlled processes, the STRUM Rabbit Polyclonal Antibody guarantees consistent performance and minimal background noise. Its superior affinity and selectivity make it an ideal choice for researchers seeking to unravel the intricate mechanisms and roles of the STRUM protein in various biological processes. Trust in the STRUM Rabbit Polyclonal Antibody to provide you with the utmost confidence and reliability in your scientific endeavors.