TEM7 Polyclonal Antibody, 100ul Gene Editing also known as hereditary hyperekplexia

also known as hereditary hyperekplexia or congenital stiff-person syndrome

AMPK is a cellular energy sensor conserved in all eukaryotic cells

This protein possesses 3' to 5' exonuclease activity

Delivered in a sturdy case of 50

The gene is expressed in male germ cells

TEM7 Polyclonal Antibody, 100ul Gene Editing also known as hereditary hyperekplexiaPLXDC1, also named as TEM3 and TEM7, belongs to the plexin family. PLXDC1 may interact with cortactin. PLXDC1 (TEM7) is identified through serial analysis of gene expression on endothelial cells isolated from human normal and malignant colorectal tissues. The antibody recognizes isoform1 and isoform4 of PLXDC1.