M3K12 Polyclonal Antibody, 100ul sgRNA customized design Defects in this gene are

Defects in this gene are a cause of epilepsy female-restricted with mental retardation (EFMR)

The protein encoded by this gene has similarity to a mouse protein which suggests a role in the insertion of secretory and membrane polypeptides into the endoplasmic reticulum

DNase/RNase-free protection for precise and accurate pipetting at 0

which is a ubiquitously expressed nuclear protein

Three transcript variants have been described for this gene

M3K12 Polyclonal Antibody, 100ul sgRNA customized design Defects in this gene areThis gene encodes a member of the serine threonine protein kinase family. This kinase contains a leucine zipper domain and is predominately expressed in neuronal cells. The phosphorylation state of this kinase in synaptic terminals was shown to be regulated by membrane depolarization via calcineurin. This kinase forms heterodimers with leucine zipper containing transcription factors, such as cAMP responsive element binding protein (CREB) and MYC, and