SEC20 Polyclonal Antibody, 20ul Cell Culture Mutations in this gene cause

Mutations in this gene cause abnormal migration of neurons during development and disrupt the layering of the cortex

It plays an important role in the suppression of proliferation-associated genes

MIM 173515) and GP5

Interacts with HEXIM1 and MAP1S

Members of this family interact with Rho family GTPases and regulate the organization of the actin cytoskeleton

SEC20 Polyclonal Antibody, 20ul Cell Culture Mutations in this gene causeThis gene is a member of the BCL2 adenovirus E1B 19 kd interacting protein (BNIP) family. It interacts with the E1B 19 kDa protein, which protects cells from virally induced cell death. The encoded protein also interacts with E1B 19 kDa like sequences of BCL2, another apoptotic protector. In addition, this protein is involved in vesicle transport into the endoplasmic reticulum. Alternative splicing of this gene results in four protein products with