LKB1 Polyclonal Antibody, 20ul[BT-AP05040] Subcellular Fractions Take your research to new

Take your research to new heights with LightNing™ PspGI (EcoRII) Restriction Enzymes

Alternatively spliced transcript variants have been observed for this gene

and seven LRRs (aa 739-988)

Mutations in this gene and H6PD (hexose-6-phosphate dehydrogenase (glucose 1-dehydrogenase)) are the cause of cortisone reductase deficiency

It plays an essential role in T-cell interactions and also in T-cell/B-cell interaction during early lymphoid development

LKB1 Polyclonal Antibody, 20ul[BT-AP05040] Subcellular Fractions Take your research to newSTK11 (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