PSPC1 Polyclonal Antibody, 100ul Lysosome Mutations in this gene cause

Mutations in this gene cause lissencephaly 4

The channel can be opened| however| by certain anesthetics| membrane stretching| intracellular acidosis| and heat

Mutations in this gene are associated with multiple endocrine neoplasia type IV (MEN4)

This gene encodes a protein that is a member of the dickkopf family

PSPC1 Polyclonal Antibody, 100ul Lysosome Mutations in this gene causeThis gene encodes a nucleolar protein that localizes to punctate subnuclear structures that occur close to splicing speckles, known as paraspeckles. These paraspeckles are composed of RNA protein structures that include a non coding RNA, NEAT1 Men epsilon beta, and the Drosophila Behavior Human Splicing family of proteins, which include the product of this gene and the P54NRB NONO and PSF SFPQ proteins. Paraspeckles may function in the control of gene