MEK3 Rabbit Polyclonal Antibody, 100ul Protein Post-translational Modification Mutations in this gene have

Mutations in this gene have been associated with disruption of the retinal pigment epithelium (RPE) phagocytosis pathway and onset of autosomal recessive retinitis pigmentosa (RP)

Dejerine-Sottas syndrome

Mutations in this gene can cause early-onset axonal neuropathy

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RAD17 checkpoint clamp loader component shares strong similarity with DNA replication factor C (RFC)

MEK3 Rabbit Polyclonal Antibody, 100ul Protein Post-translational Modification Mutations in this gene haveThe protein encoded by this gene is a dual specificity protein kinase that belongs to the MAP kinase kinase family. This kinase is activated by mitogenic and environmental stress, and participates in the MAP kinase mediated signaling cascade. It phosphorylates and thus activates MAPK14 p38 MAPK. This kinase can be activated by insulin, and is necessary for the expression of glucose transporter. Expression of RAS oncogene is found to result in the