VHLL Rabbit Polyclonal Antibody, 100ul Transporters one JmjC domain

one JmjC domain

Multiple alternatively spliced transcript variants of this gene encoding distinct isoforms have been reported

Specific mutations in DYSF have been shown to cause autosomal recessive limb girdle muscular dystrophy type 2B (LGMD2B) as well as Miyoshi myopathy

Regulator of G protein signaling (RGS) family members are regulatory molecules that act as GTPase activating proteins (GAPs) for G alpha subunits of heterotrimeric G proteins

Alternative splicing of this gene results in multiple transcript variants encoding different isoforms containing c-terminal dbl oncogene homology (DH) and pleckstrin homology (PH) domains

VHLL Rabbit Polyclonal Antibody, 100ul Transporters one JmjC domain