MK12 Polyclonal Antibody, 100ul Recombinant Ab Production Defects in this gene are

Defects in this gene are a cause of hereditary coproporphyria (HCP)

This gene encodes a member of the glucose phosphate isomerase protein family

The protein encoded by this gene is a helix-loop-helix (HLH) protein that can form heterodimers with other HLH proteins

Posttranslational modifications determine whether this protein localizes to the nucleus or the cytoplasm

Defects in this factor lead to Rosenthal syndrome| a blood coagulation abnormality

MK12 Polyclonal Antibody, 100ul Recombinant Ab Production Defects in this gene areActivation of members of the mitogen activated protein kinase family is a major mechanism for transduction of extracellular signals. Stress activated protein kinases are one subclass of MAP kinases. The protein encoded by this gene functions as a signal transducer during differentiation of myoblasts to myotubes.