Background：Hearing impairment is a heterogeneous condition with over 40 loci described. The protein encoded by this gene is expressed in fetal cochlea, however, its function is not known. Nonsyndromic hearing impairment is associated with a mutation in this gene. Three transcript variants encoding two different isoforms have been found for this gene.
仕様
Synonyms：2310037D07Rik,4932441K13Rik,Deafness,autosomal dominant 5,Deafness,autosomal dominant 5 protein,DFNA5,DFNA5 gene,DFNA5,Dfna5h,EG14210,Fin15,ICERE 1,ICERE-1,Inversely correlated with estrogen receptor expression 1,Non-syndromic hearing impairment protein 5,Nonsyndromic hearing impairment protein
Host：Rabbit
Reactivity：Human,Mouse,Rat
Applications：WB,IHC
Concentration：1mg/ml
Immunogen：Recombinant protein of human DFNA5
Purification Method：Affinity purification
Clonality：Polyclonal
Conjugation：Unconjugated
Buffer：Buffer： PBS with 0.02％ sodium azide, 50％ glycerol, pH7.3.
