LKB1 Polyclonal Antibody, 20ul[BT-AP05039] Cellular Function Assays peripheral blood lymphocytes and bone

peripheral blood lymphocytes and bone marrow

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

and axial skeleton

The encoded protein (mannan binding lectin serine peptidase 1) is synthesized as a zymogen and is activated when it complexes with the pathogen recognition molecules of lectin pathway

Excellent mixing (200-1500rpm)

LKB1 Polyclonal Antibody, 20ul[BT-AP05039] Cellular Function Assays peripheral blood lymphocytes and boneSTK11 (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