NSD1 is a histone methyltransferase that preferentially methylates Lys-36 of histone H3 and Lys-20 of histone H4. NSD1 can function as an androgen receptor coactivator and is capable of both negatively and positively influencing transcription. Mutations in NSD1 are responsible for Sotos syndrome, Weaver syndrome, Beckwith-Wiedemann syndrome, and a form of childhood leukemia.
Alternative names for
NSD1 IHC Antibody include NSD1 antibody, NSD-1 antibody, nuclear receptor binding SET domain protein 1 antibody, ARA267 antibody, ARA-267 antibody, androgen receptor-associated coregulator 267 antibody, STO antibody, SOTOS antibody, Sotos syndrome antibody, FLJ22263 antibody.