NOTCH4 (Cleaved-Val1467) Rabbit Polyclonal Antibody, 20ul Mini dry bath It is localized in nuclear

It is localized in nuclear bodies of the nucleus

It is thought that this protein functions to regulate iron absorption by regulating the interaction of the transferrin receptor with transferrin

Mutations in this gene can cause combined oxidative phosphorylation deficiency 14 (Alpers encephalopathy)

Serpin family B member 9 inhibits the activity of the effector molecule granzyme B

The protein described in this record is a light chain and exists as part of this complex but also physically interacts with and inhibits the activity of neuronal nitric oxide synthase

NOTCH4 (Cleaved-Val1467) Rabbit Polyclonal Antibody, 20ul Mini dry bath It is localized in nuclearThis gene encodes a member of the NOTCH family of proteins. Members of this Type I transmembrane protein family share structural characteristics including an extracellular domain consisting of multiple epidermal growth factor like (EGF) repeats and an intracellular domain consisting of multiple different domain types. Notch signaling is an evolutionarily conserved intercellular signaling pathway that regulates interactions between physically adjacent