The protein encoded by this gene is a transcription factornthat can act as a homodimer or as a heterodimer with either GRHL1nor GRHL3. Defects in this gene are a cause of non-syndromicnsensorineural deafness autosomal dominant type 28 (DFNA28).
应用类型
WB
免疫原
This GRHL2 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 409-438 amino acids from the Central region of human GRHL2.
