SLC6A8 Polyclonal Antibody, 50ul Lentiviral Packaging PLXDC1 (TEM7) is identified through

PLXDC1 (TEM7) is identified through serial analysis of gene expression on endothelial cells isolated from human normal and malignant colorectal tissues

This gene is located in a region of chromosome 14 frequently showing unparental disomy

which form the mature heterodimer

frequently involved in chromosomal rearrangements

Mutations in this gene were found in individuals with osteogenesis imperfecta

SLC6A8 Polyclonal Antibody, 50ul Lentiviral Packaging PLXDC1 (TEM7) is identified throughSodium and chloride dependent creatine transporter 1 encoded by SLC6A8 is a plasma membrane protein whose function is to transport creatine into and out of cells. Defects in this gene can result in X linked creatine deficiency syndrome. Multiple transcript variants encoding different isoforms have been found for this gene.