Synapsin-1 Polyclonal Antibody, 50ul Isothermal Amplification Defects in PARK7 are the

Defects in PARK7 are the cause of autosomal recessive early-onset Parkinson disease 7

Ephrin A2 is composed of a signal sequence

Increased expression of this gene has been reported in a variety of tumor types

tissue specificity:Found in ovarian granulosa cells

RAN is a small GTP-binding protein of the RAS superfamily that is associated with the nuclear membrane and is thought to control a variety of cellular functions through its interactions with other proteins

Synapsin-1 Polyclonal Antibody, 50ul Isothermal Amplification Defects in PARK7 are theSYN1 (synapsin I) is a member of the synapsin gene family. Synapsins encode neuronal phosphoproteins which associate with the cytoplasmic surface of synaptic vesicles. Family members are characterized by common protein domains, and they are implicated in synaptogenesis and the modulation of neurotransmitter release, suggesting a potential role in several neuropsychiatric diseases. This member of the synapsin family plays a role in regulation of