RB39B Polyclonal Antibody, 100ul Stepper Studies suggest certain mutations in

Studies suggest certain mutations in this gene lead to childhood absence epilepsy (CAE)

The encoded product shares strong homology with the C

A2M is implicated in Alzheimer disease (AD) due to its ability to mediate the clearance and degradation of A-beta

studies in rodents suggest that it is a transcriptional inhibitor in the absence of Ras

MARV and EBOV GP1

RB39B Polyclonal Antibody, 100ul Stepper Studies suggest certain mutations inThis gene encodes a member of the Rab family of proteins. Rab proteins are small GTPases that are involved in vesicular trafficking. Mutations in this gene are associated with X linked mental retardation.