ARHGEF9 Polyclonal Antibody, 20ul Cell Culture ALK/TPM4 (chromosome 19)

ALK/TPM4 (chromosome 19)

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

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

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ARHGEF9 Polyclonal Antibody, 20ul Cell Culture ALK/TPM4 (chromosome 19)The 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.