Gl Syn Polyclonal Antibody, 50ul[BT-AP15735] Vacuum Aspirator Defects in this gene have

Defects in this gene have been linked to infertility| problems with gluconeogenesis and lipogenesis| and altered sleep patterns

The SFPQ-NONO heteromer associated with MATR3 may play a role in nuclear retention of defective RNAs

GPRIN1 is a Protein Coding gene

Mutations in this gene cause X-linked severe combined immunodeficiency (XSCID)

Catalytic activity:ATP + H(2)O = ADP + phosphate

Gl Syn Polyclonal Antibody, 50ul[BT-AP15735] Vacuum Aspirator Defects in this gene haveThe protein encoded by this gene belongs to the glutamine synthetase family. It catalyzes the synthesis of glutamine from glutamate and ammonia in an ATP dependent reaction. This protein plays a role in ammonia and glutamate detoxification, acid base homeostasis, cell signaling, and cell proliferation. Glutamine is an abundant amino acid, and is important to the biosynthesis of several amino acids, pyrimidines, and purines. Mutations in this gene are