Background：The protein encoded by this gene is an enzyme that covalently links a heme group to the apoprotein of cytochrome c. Defects in this gene are a cause of microphthalmia syndromic type 7 （MCOPS7）. Three transcript variants encoding the same protein have been found for this gene.
仕様
Synonyms：CCHL,CCHL,cytochrome c heme-lyase,Cytochrome c-type heme lyase,DKFZp779I1858,EC 4.4.1.17,Hccs,Holocytochrome c synthase （cytochrome c heme lyase）,Holocytochrome c synthase,Holocytochrome c type synthase,Holocytochrome c-type synthase,MCOPS7,OTTHUMP00000022903,OTTHUMP00000022904,OTTHUMP00000022905,OTTMUSP00000021173,OTTMUSP00000021174,RGD1563855,RP23-37L2.1
Host：Rabbit
Reactivity：Human,Mouse,Rat
Applications：WB
Concentration：1mg/ml
Immunogen：Recombinant protein of human HCCS
Purification Method：Affinity purification
Clonality：Polyclonal
Conjugation：Unconjugated
Buffer：Buffer： PBS with 0.02％ sodium azide, 50％ glycerol, pH7.3.
