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.

Codice: E-AB-18958_60μL | Marca: Elabscience | Confezionamento: 60μL

Specie: Human;MouseIsotipo: IgGConiugazione: Unconjugated

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Codice: E-AB-18958_60μL
Marca: Elabscience
Specie target: Human;Mouse
Host: Rabbit
Concentrazione: 1.98 mg/mL
Link: Apri link
Stoccaggio: Store at -20℃ Valid for 12 months. Avoid freeze / thaw cycles.
Isotipo: IgG
Clonalità: Polyclonal
Coniugazione: Unconjugated
Applicazione: WB;IHC
Diluizione: WB 1:5000-1:10000;IHC 1:50-1:300
Simbolo target: HCCS
Ig target: 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
Area di ricerca: Cancer;Cardiovascular;Metabolism;Signal Transduction

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