RTKN2 Rabbit Polyclonal Antibody, 50ul Gene Synthesis KLHL3 is ubiquitously expressed and

KLHL3 is ubiquitously expressed and encodes kelch like family member 3 which has an N-terminal BTB domain followed by a BACK domain and six kelch-like repeats in the C-terminus

This gene encodes a member of a family of proteins containing one or more high mobility group DNA-binding motifs

This gene encodes a G protein-coupled receptor (GPCR) that belongs to the oxoglutarate receptor family within the GPCR superfamily

Mutations in DLX3 have been associated with the autosomal dominant conditions trichodentoosseous syndrome and amelogenesis imperfecta with taurodontism

|disease:Defects in EP300 are a cause of Rubinstein-Taybi syndrome (RSTS)

RTKN2 Rabbit Polyclonal Antibody, 50ul Gene Synthesis KLHL3 is ubiquitously expressed and