PAR11 Polyclonal Antibody, 100ul Vacuum Aspirator and a highly conservative 13-consecutive-histidine

and a highly conservative 13-consecutive-histidine repeat

Defects in this gene appear to be a cause of various types of leukemia or lymphoma

Alternative splicing or deletion caused by a translocation event in this paternally-expressed region is responsible for Angelman syndrome or Prader-Willi syndrome due to parental imprint switch failure

Mutations in this gene cause hereditary lymphedema type IA

PAR11 Polyclonal Antibody, 100ul Vacuum Aspirator and a highly conservative 13-consecutive-histidineCatalytic activity: NAD(+) + (ADP D ribosyl)(n) acceptor = nicotinamide + (ADP D ribosyl)(n+1) acceptor.,Contains 1 PARP catalytic domain.,Contains 1 WWE domain.,