WNK1 Polyclonal Antibody, 20ul Live Cell Imaging GGT7 is a member of

GGT7 is a member of a gene family that encodes enzymes involved in both the metabolism of glutathione and in the transpeptidation of amino acids

Defects in this gene are the cause of LIG4 syndrome

All GTPases of the Ras superfamily have in common the presence of six conserved motifs involved in GTP/GDP binding

and RNA processing and transport

The protein encoded by RFX2 is structurally related to regulatory factors X1

WNK1 Polyclonal Antibody, 20ul Live Cell Imaging GGT7 is a member ofWNK1 encodes a member of the WNK subfamily of serine threonine protein kinases. The serine threonine protein kinase WNK1 may be a key regulator of blood pressure by controlling the transport of sodium and chloride ions. Mutations in this gene have been associated with pseudohypoaldosteronism type II and hereditary sensory neuropathy type II. Alternatively spliced transcript variants encoding different isoforms have been described but the full length