SPRE1 Polyclonal Antibody, 100ul Endonucleases & Exonucleases suggesting that it is required

suggesting that it is required for kinetochore formation

disease:A chromosomal aberration involving NUT is found in a rare

serum glycoprotein turnover

which is an ATP-binding cleft

The encoded protein is part of a complex that responds to beta-adrenergic signals by inhibiting adenylate cyclase

SPRE1 Polyclonal Antibody, 100ul Endonucleases & Exonucleases suggesting that it is requiredThe protein encoded by this gene is a member of the Sprouty family of proteins and is phosphorylated by tyrosine kinase in response to several growth factors. The encoded protein can act as a homodimer or as a heterodimer with SPRED2 to regulate activation of the MAP kinase cascade. Defects in this gene are a cause of neurofibromatosis type 1 like syndrome (NFLS).