HoxD12 Polyclonal Antibody, 50ul Drug Development and Evaluation these pipets are perfect for

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Mutations in this gene have be associated glycogen storage disease

Mutations in this gene can cause combined oxidative phosphorylation deficiency 14 (Alpers encephalopathy)

It is thought that this pathway contributes to Rho-induced reorganization of the actin cytoskeleton

HoxD12 Polyclonal Antibody, 50ul Drug Development and Evaluation these pipets are perfect forHOXD12 belongs to the homeobox family of genes. The homeobox genes encode a highly conserved family of transcription factors that play an important role in morphogenesis in all multicellular organisms. Mammals possess four similar homeobox gene clusters, HOXA, HOXB, HOXC and HOXD, located on different chromosomes, consisting of 9 to 11 genes arranged in tandem. HOXD12 is one of several homeobox HOXD genes located in a cluster on chromosome 2.