LKB1(Phospho Ser334) Polyclonal Antibody, 50ul Protein Modification and in the regulation of

and in the regulation of interferon-inducible genes

Defects in EP300 are a cause of Rubinstein-Taybi syndrome and may also play a role in epithelial cancer

The CDK subfamily members are highly similar to the gene products of S

MYO1D (Myosin ID) is a Protein Coding gene

The RING finger and B-box domains chelate zinc and might be involved in protein-protein and/or protein-nucleic acid interactions

LKB1(Phospho Ser334) Polyclonal Antibody, 50ul Protein Modification and in the regulation ofThis 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