TAL1(Phospho Ser122) Polyclonal Antibody, 50ul Microbial Genome Editing This is supported by studies

This is supported by studies in knockout mice showing development of soft-tissue sarcomas

This gene is located in a chromosomal region known to be frequently deleted in patients with neurofibromatosis

Mutations in this gene are associated with hereditary long QT syndrome 1 (also known as Romano-Ward syndrome)

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Cut like homeobox 1 encoded by CUX1 is a member of the homeodomain family of DNA binding proteins

TAL1(Phospho Ser122) Polyclonal Antibody, 50ul Microbial Genome Editing This is supported by studiesalternative 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