MKK7(Phospho-Ser271/Thr275) Rabbit Polyclonal Antibody, 100ul Immunoassays Mutations in this gene have

Mutations in this gene have been associated with bare lymphocyte syndrome type II (also known as hereditary MHC class II deficiency or HLA class II-deficient combined immunodeficiency)

part of the post-replicative DNA mismatch repair system

SERPINB7 (serpin family B member 7) encodes a member of a family of proteins which function as protease inhibitors

Notch 2 functions as a receptor for membrane bound ligands

MKK7(Phospho-Ser271/Thr275) Rabbit Polyclonal Antibody, 100ul Immunoassays 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 specifically activates MAPK8 JNK1 and MAPK9 JNK2 and this kinase itself is phosphorylated and activated by MAP kinase kinase kinases including MAP3K1 MEKK1 MAP3K2 MEKK2 MAP3K3 MEKK5 and MAP4K2 GCK. This kinase is involved in the signal transduction mediating the cell responses to proinflammatory cytokines and environmental