GLMN Polyclonal Antibody, 20ul Peptide Library This gene encodes a member

This gene encodes a member of the basic-leucine zipper family and the AMP-dependent transcription factor family

Defects in this gene are the cause of glycogen storage disease II| also known as Pompe's disease| which is an autosomal recessive disorder with a broad clinical spectrum

FOXO1 belongs to the forkhead family of transcription factors which are characterized by a distinct forkhead domain

The product of CKLF (chemokine like factor) is a cytokine

GLMN Polyclonal Antibody, 20ul Peptide Library This gene encodes a memberThis gene encodes a phosphorylated protein that is a member of a Skp1 Cullin F box like complex. The protein is essential for normal development of the vasculature and mutations in this gene have been associated with glomuvenous malformations, also called glomangiomas. Multiple splice variants encoding different isoforms have been found for this gene.