GIMAP5 Polyclonal Antibody, 50ul Low-speed Centrifuges Defects in EDA are a

Defects in EDA are a cause of ectodermal dysplasia

This protein is absent in patients with Duchenne and Becker types of muscular dystrophy

It is thought to function in cardiomyocyte expansion and in restraining postsynaptic growth of excitatory synapses

The protein belongs to the L4E family of ribosomal proteins

Alternative splicing generates additional isoforms of each of the five growth hormones

GIMAP5 Polyclonal Antibody, 50ul Low-speed Centrifuges Defects in EDA are aGIMAP5 encodes GTPase IMAP family member 5 belonging to the GTP binding superfamily and to the immuno associated nucleotide (IAN) subfamily of nucleotide binding proteins. In humans, the IAN subfamily genes are located in a cluster at 7q36. GIMAP5 encodes an antiapoptotic protein that functions in T cell survival. Polymorphisms in this gene are associated with systemic lupus erythematosus. Read through transcription exists between GIMAP5 and the