TAL1/2 (Acetyl Lys221/Acetyl Lys222/Acetyl Lys36/Acetyl Lys37) Polyclonal Antibody, 50ul Immunology or Elejalde disease

or Elejalde disease

as well as maturity onset diabetes of the young type 4 (MODY4)

Mutations associated with this gene cause autosomal recessive spastic paraplegia 13

Studies in mice suggest that the encoded protein is necessary for the rapid acute-phase response to LPS but not for the clearance of LPS from circulation

This protein regulates gene expression induced by osmotic stress in mammalian cells

TAL1/2 (Acetyl Lys221/Acetyl Lys222/Acetyl Lys36/Acetyl Lys37) Polyclonal Antibody, 50ul Immunology or Elejalde diseasealternative products: The splicing pattern is cell lineage dependent disease: A chromosomal aberration involving TAL1 may be a cause of some T cell acute lymphoblastic leukemias (T ALL). Translocation t(1; 14)(p32; q11) with T cell receptor alpha chain (TCRA) genes. The helix loop helix domain is necessary and sufficient for the interaction with DRG1. Implicated in the genesis of hemopoietic malignancies. It may play an important role in hemopoietic