RPGF6 Polyclonal Antibody, 100ul Cell fragmentation and collection Mutations in this gene are

Mutations in this gene are associated with septooptic dysplasia

but contains other ADAMTS domains

This gene is located between the Charcot-Marie-Tooth and Smith-Magenis syndrome critical regions on chromosome 17

With easy storage at 2-8℃ for maximum stability

The encoded protein catalyzes the dephosphorylation of phosphotyrosine and phosphatidylinositol and plays roles in cellular proliferation and differentiation

RPGF6 Polyclonal Antibody, 100ul Cell fragmentation and collection Mutations in this gene areGuanine nucleotide exchange factor (GEF) for Rap1A, Rap2A and M Ras GTPases. Does not interact with cAMP.,PTM: Phosphorylated upon DNA damage, probably by ATM or ATR.,Contains 1 cyclic nucleotide binding domain.,Contains 1 N terminal Ras GEF domain.,Contains 1 PDZ (DHR) domain.,Contains 1 Ras associating domain.,Contains 1 Ras GEF domain.,subcellular location: Upon binding to M Ras, it translocates to the plasma membrane.,subunit: Interacts with the