Ezrin(Phospho Thr566) Polyclonal Antibody, 20ul Monoclonal Antibodies Mutations in SGCA result in

Mutations in SGCA result in type 2D autosomal recessive limb-girdle muscular dystrophy

The encoded protein is a subunit of the core-TFIIH basal transcription factor and localizes to the nucleus

observation and labeling

is responsible for the deamination of adenosine 37 to inosine in eukaryotic tRNA

K-HECT subfamily

Ezrin(Phospho Thr566) Polyclonal Antibody, 20ul Monoclonal Antibodies Mutations in SGCA result inThe cytoplasmic peripheral membrane protein encoded by this gene functions as a protein tyrosine kinase substrate in microvilli. As a member of the ERM protein family, this protein serves as an intermediate between the plasma membrane and the actin cytoskeleton. This protein plays a key role in cell surface structure adhesion, migration and organization, and it has been implicated in various human cancers. A pseudogene located on chromosome 3 has been