TBX15 Polyclonal Antibody, 100ul Liquid Handling ＆Storage |disease:A chromosomal aberration involving NFKB2

|disease:A chromosomal aberration involving NFKB2 is found in a cutaneous T-cell leukemia (C-TCL) cell line

Members of the trefoil family are characterized by having at least one copy of the trefoil motif

The myeloid cell nuclear differentiation antigen (MNDA) is detected only in nuclei of cells of the granulocyte-monocyte lineage

slow skeletal-

Mitotic kinesin required for chromosome passenger complex (CPC)-mediated cytokinesis

TBX15 Polyclonal Antibody, 100ul Liquid Handling ＆Storage |disease:A chromosomal aberration involving NFKB2This gene belongs to the T box family of genes, which encode a phylogenetically conserved family of transcription factors that regulate a variety of developmental processes. All these genes contain a common T box DNA binding domain. Mutations in this gene are associated with Cousin syndrome.