ARHGEF9 Polyclonal Antibody, 20ul Cell Culture Human-derived DNA-free

Human-derived DNA-free

Don't compromise on your lab results - choose the VT1

Three transcript variants encoding different isoforms have been found for this gene

alpha actinin isoform and maps to the same site as the structurally similar erythroid beta spectrin gene

All known peroxisomal ABC transporters are half transporters which require a partner half transporter molecule to form a functional homodimeric or heterodimeric transporter

ARHGEF9 Polyclonal Antibody, 20ul Cell Culture Human-derived DNA-freeThe Cdc42 guanine nucleotide exchange factor 9 encoded by ARHGEF9 is a Rho like GTPase that switches between the active (GTP bound) state and inactive (GDP bound) state to regulate CDC42 and other genes. Defects in this gene are a cause of startle disease with epilepsy (STHEE), also known as hyperekplexia with epilepsy. Three transcript variants encoding different isoforms have been found for this gene.