Megsin Polyclonal Antibody, 100ul ssDNA Synthesis also known as high affinity

also known as high affinity nerve growth factor receptor

Mutations in this gene may be associated with X-linked disorders with primary neuronal degeneration such as Rett syndrome

two FY-rich domains

Has a role in myogenic differentiation and in remodeling processes of adult muscles that occur in response to physiological stimuli

Mutations in TSC1 have been associated with tuberous sclerosis

Megsin Polyclonal Antibody, 100ul ssDNA Synthesis also known as high affinitySERPINB7 (serpin family B member 7) encodes a member of a family of proteins which function as protease inhibitors. Expression of SERPINB7 is upregulated in IgA nephropathy and mutations have been found to cause palmoplantar keratoderma, Nagashima type. Alternative splicing results in multiple transcript variants.