FoxO4 Polyclonal Antibody, 50ul[BT-AP03337] Cell Separation and Collection a craniofacial development disorder

a craniofacial development disorder

Stathmin proteins function in microtubule dynamics and signal transduction

Mutations in this gene cause ribose 5-phosphate isomerase deficiency

This gene encodes a member of the group 2 decarboxylase family

is located in the mitochondria and expressed in extra-hepatic tissues

FoxO4 Polyclonal Antibody, 50ul[BT-AP03337] Cell Separation and Collection a craniofacial development disorderFOXO4 encodes a member of the O class of winged helix forkhead transcription factor family. Proteins encoded by this class are regulated by factors involved in growth and differentiation indicating they play a role in these processes. A translocation involving this gene on chromosome X and the homolog of the Drosophila trithorax gene, encoding a DNA binding protein, located on chromosome 11 is associated with leukemia. Multiple transcript variants