SEK1 Polyclonal Antibody, 100ul Sampling Tubes Defects in this gene are

Defects in this gene are a cause of startle disease with epilepsy (STHEE)

amygdala and olfactory bulb and is thought to play an important role in neuronal migration and axonal projection

Overexpression of this gene in COS7 cells stimulates translation

The protein encoded by this gene represents a regulatory subunit of PI3K

SEK1 Polyclonal Antibody, 100ul Sampling Tubes Defects in this gene areMAP2K4 encodes a member of the mitogen activated protein kinase (MAPK) family. Members of this family act as an integration point for multiple biochemical signals and are involved in a wide variety of cellular processes such as proliferation, differentiation, transcription regulation, and development. They form a three tiered signaling module composed of MAPKKKs, MAPKKs, and MAPKs. Dual specificity mitogen activated protein kinase kinase 4 is