LKB1(Phospho Thr189) Polyclonal Antibody, 20ul ROS/Nitric Oxide Detection is important for DNA double-strand

is important for DNA double-strand break repair

Mutations in NRXN1 are associated with Pitt-Hopkins-like syndrome-2 and may contribute to susceptibility to schizophrenia

hepatocellular carcinomas

The protein encoded by this gene is a major apoprotein of the chylomicron

and more specifically

LKB1(Phospho Thr189) Polyclonal Antibody, 20ul ROS/Nitric Oxide Detection is important for DNA double-strandThis gene, which encodes a member of the serine threonine kinase family, regulates cell polarity and functions as a tumor suppressor. Mutations in this gene have been associated with Peutz Jeghers syndrome, an autosomal dominant disorder characterized by the growth of polyps in the gastrointestinal tract, pigmented macules on the skin and mouth, and other neoplasms. Alternate transcriptional splice variants of this gene have been observed but have not