Background：The protein encoded by this gene is a homeodomain-containing transcription factor that appears to function in the regulation of organogenesis. This gene is located downstream of the dystrophia myotonica-protein kinase gene. Mutations in this gene are a cause of branchiootorenal syndrome type 2.SIX5 （SIX Homeobox 5） is a Protein Coding gene. Diseases associated with SIX5 include Branchiootorenal Syndrome 2 and Branchiootorenal Syndrome. GO annotations related to this gene include sequence-specific DNA binding. An important paralog of this gene is SIX4.
仕様
Synonyms：BOR2,DM locus associated homeodomain protein,DM locus-associated homeodomain protein,DMAHP,Dystrophia myotonica associated homeodomain protein,Homeobox protein SIX5,Sine oculis homeobox homolog 5,sine oculis related homeobox 5 homolog （Drosophila）,SIX homeobox 5,SIX5,SIX5
Host：Rabbit
Reactivity：Human,Mouse
Applications：WB,ELISA
Concentration：1mg/mL
Immunogen：Synthesized peptide derived from the Internal region of human Six5
Purification Method：Affinity purification
Clonality：Polyclonal
Conjugation：Unconjugated
Buffer：PBS with 0.02％ sodium azide,0.5％ BSA and 50％ glycerol pH 7.4.
