SPEG Polyclonal Antibody, 20ul Organelle Studies The predicted 727-amino acid human

The predicted 727-amino acid human protein contains a 29-amino acid presequence

PPARs mediate a variety of biological processes

Alterations of this gene| including point mutations| insertions and deletions| cause factor IX deficiency| which is a recessive X-linked disorder| also called hemophilia B or Christmas disease

The enzyme may be involved in several physiological processes including cell contraction

SPEG Polyclonal Antibody, 20ul Organelle Studies The predicted 727-amino acid humanThis gene encodes a protein with similarity to members of the myosin light chain kinase family. This protein family is required for myocyte cytoskeletal development. Along with the desmin gene, expression of this gene may be controlled by the desmin locus control region. Mutations in this gene are associated with centronuclear myopathy 5.