Background：The mouse ortholog of this protein co-purifies with the mitochondrial inner membrane. Mutations in this gene have been shown to result in 3-methylglutaconic aciduria type III and autosomal dominant optic atrophy and cataract. Multiple transcript variants encoding different isoforms have been found for this gene.
仕様
Synonyms：FLJ22187,FLJ25932,Iraqi Jewish optic atrophy plus （3 methylglutaconicaciduria type 3）,MGA3 ,MGC75494,OPA 3,OPA3 protein,Optic atrophy 3 （autosomal recessive, with chorea and spastic paraplegia）,Optic atrophy 3 （Iraqi Jewish 'optic atrophy plus'）,Optic atrophy 3,Optic atrophy 3 protein
Host：Rabbit
Reactivity：Human,Mouse,Rat
Applications：WB,IHC
Concentration：1mg/ml
Immunogen：Recombinant protein of human OPA3
Purification Method：Affinity purification
Clonality：Polyclonal
Conjugation：Unconjugated
Buffer：Buffer： PBS with 0.02％ sodium azide, 50％ glycerol, pH7.3.
