IKK alpha(Phospho Thr23) Polyclonal Antibody, 100ul Cell Screening and Imaging Defects in this protein or

Defects in this protein or in its signalling pathway are a cause of holoprosencephaly (HPE)

and glibenclamide

Members of this family are required for cytokinesis

Mutation in this gene has been associated with Amish infantile epilepsy syndrome

we are able to provide humanized antibodies with diminished immunogenicity

IKK alpha(Phospho Thr23) Polyclonal Antibody, 100ul Cell Screening and Imaging Defects in this protein orThis gene encodes a member of the serine threonine protein kinase family. The encoded protein a component of a cytokine activated protein complex that is an inhibitor of the essential transcription factor NF kappa B complex phosphorylates sites that trigger the degradation of the inhibitor via the ubiquination pathway thereby activating the transcription factor.