LKB1 Polyclonal Antibody, 20ul[BT-AP05039] Cellular Function Assays Unleash your potential with our

Unleash your potential with our Human TGF-α ELISA KIT-96T

Alternatively spliced transcript variants encoding multiple isoforms have been observed for CASP2

Its two SH3 domains direct complex formation with proline-rich regions of other proteins

This kinase is localized in the nucleus

Defects in GJC2 are the cause of autosomal recessive Pelizaeus-Merzbacher-like disease-1

LKB1 Polyclonal Antibody, 20ul[BT-AP05039] Cellular Function Assays Unleash your potential with ourSTK11 (serine threonine kinase 11), which encodes a member of the serine threonine kinase family, regulates cell polarity and functions as a tumor suppressor. Mutations in STK11 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 STK11 have been