DLX1 Polyclonal Antibody, 100ul Cellular Function Assays a relatively common human disorder

a relatively common human disorder with phenotypic features including cleft palate

U3 small nucleolar ribonucleoprotein) encodes the human homolog of the yeast Imp3 protein

nucleotide excision repair protein contains an N-terminal ubiquitin-like domain

which was also identified as a cellular transcription factor that binds to an enhancer in the promoter of the T cell leukemia virus type 1 promoter

Transcriptional activator that binds to the enhancer of the adenovirus E1A gene

DLX1 Polyclonal Antibody, 100ul Cellular Function Assays a relatively common human disorderThis gene encodes a member of a homeobox transcription factor gene family similiar to the Drosophila distal less gene. The encoded protein is localized to the nucleus where it may function as a transcriptional regulator of signals from multiple TGF {beta} superfamily members. The encoded protein may play a role in the control of craniofacial patterning and the differentiation and survival of inhibitory neurons in the forebrain. This gene is located in