LKB1(Phospho Ser334) Polyclonal Antibody, 100ul Reagent Reservoirs Defects in this gene are

Defects in this gene are associated with osteogenesis imperfecta| a connective tissue disorder characterized by bone fragility and low bone mass

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BTC encodes a member of the epidermal growth factor (EGF) family of proteins

CSA or DDB2

LKB1(Phospho Ser334) Polyclonal Antibody, 100ul Reagent Reservoirs Defects in this gene areThis 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