GSTT1/4 Polyclonal Antibody, 50ul Peripheral Blood Separation Tube Alternative splicing or deletion caused

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

This gene encodes a protein that may function in neuron survival

and like the mouse gene

NXPH4is a Protein Coding gene

The gene maps to the region on chromosome 22q11

GSTT1/4 Polyclonal Antibody, 50ul Peripheral Blood Separation Tube Alternative splicing or deletion causedGlutathione S transferase theta 1 encoded by GSTT1 is a member of a superfamily of proteins that catalyze the conjugation of reduced glutathione to a variety of electrophilic and hydrophobic compounds. Human GSTs can be divided into five main classes: alpha, mu, pi, theta, and zeta. The theta class includes GSTT1, GSTT2, and GSTT2B. GSTT1 and GSTT2 GSTT2B share 55% amino acid sequence identity and may play a role in human carcinogenesis. The GSTT1