IRPL1 Polyclonal Antibody, 100ul Cell Senescence Alternatively spliced transcript variants encoding

Alternatively spliced transcript variants encoding different isoforms have been noted for PPP1R14A

The protein encoded by MED14 (mediator complex subunit 14) is a subunit of the CRSP (cofactor required for SP1 activation) complex

Mutations in ITCH are a cause of syndromic multisystem autoimmune disease

a state which is disrupted by inhibition of this novel serine protease

Mutations in the genes that code for the collagen VI subunits result in the autosomal dominant disorder

IRPL1 Polyclonal Antibody, 100ul Cell Senescence Alternatively spliced transcript variants encodingThe protein encoded by this gene is a member of the interleukin 1 receptor family and is similar to the interleukin 1 accessory proteins. It is most closely related to interleukin 1 receptor accessory protein like 2 (IL1RAPL2). This gene and IL1RAPL2 are located at a region on chromosome X that is associated with X linked non syndromic mental retardation. Deletions and mutations in this gene were found in patients with mental retardation. This gene is