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

EPHA7 belongs to the ephrin receptor subfamily of the protein-tyrosine kinase family

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

|Belongs to the histone deacetylase family

Zinc finger protein Aiolos is a transcription factor that is important in the regulation of B lymphocyte proliferation and differentiation

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.