TReP-132 Polyclonal Antibody, 100ul Cellular Function Assays Mutations in HK1 have been

Mutations in HK1 have been associated with hemolytic anemia due to hexokinase deficiency

TRA2A is a member of the transformer 2 homolog family and encodes a protein with several RRM (RNA recognition motif) domains

including a secreted form

an autosomal recessive disorder characterized by unregulated insulin secretion

TReP-132 Polyclonal Antibody, 100ul Cellular Function Assays Mutations in HK1 have beenTRERF1 (transcriptional regulating factor 1) encodes a zinc finger transcriptional regulating protein which interacts with CBP p300 to regulate the human gene CYP11A1. Alternative splicing results in multiple transcript variants encoding different isoforms.