SCO1 polyclonal, anti-human, mouse, rat
€388.00
In stock
SKU
BS8394
Background:
The SCO1 and SCO2 protein homologs belong to the SCO1/2 family of proteins. SCO1 and SCO2 both localize to the mitochondrion and are inner membrane proteins crucial for copper insertion or transport to the active site of cytochrome c oxidase (COX). COX is a crucial component in energy production because it functions as the terminal enzyme in the respiratory chain. SCO1 is predominantly expressed in highly oxidative phosphorylation tissues such as brain, heart and muscle, while SCO2 is ubiquitously expressed. Defects in the gene encoding for SCO1 may cause cytochrome c oxidase deficiency, a hetero-genous disorder. Defects in the gene encoding for SCO2 may cause cardioencephalomyopathy with cytochrome c oxidase deficiency, a fatal infantile disorder characterized by hypertrophic cardiomyopathy, lactic acidosis and gliosis.
Alternative Name:
Protein SCO1 homolog, mitochondrial, SCO1, SCOD1
Application Dilution: WB: 1:500~1:2000, IHC: 1:50~1:200
Specificity: SCO1 polyclonal antibody detects endogenous levels of SCO1 protein.
Immunogen:
Recombinant full length Human SCO1.
MW: ~ 34 kDa
Swis Prot.: O75880
Purification & Purity:
The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen and the purity is > 95% (by SDS-PAGE).
Format:
1mg/ml in PBS with 0.1% Sodium Azide, 50% Glycerol.
Storage:
Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze-thaw cycles.
For research use only, not for use in diagnostic procedure.
The SCO1 and SCO2 protein homologs belong to the SCO1/2 family of proteins. SCO1 and SCO2 both localize to the mitochondrion and are inner membrane proteins crucial for copper insertion or transport to the active site of cytochrome c oxidase (COX). COX is a crucial component in energy production because it functions as the terminal enzyme in the respiratory chain. SCO1 is predominantly expressed in highly oxidative phosphorylation tissues such as brain, heart and muscle, while SCO2 is ubiquitously expressed. Defects in the gene encoding for SCO1 may cause cytochrome c oxidase deficiency, a hetero-genous disorder. Defects in the gene encoding for SCO2 may cause cardioencephalomyopathy with cytochrome c oxidase deficiency, a fatal infantile disorder characterized by hypertrophic cardiomyopathy, lactic acidosis and gliosis.
Alternative Name:
Protein SCO1 homolog, mitochondrial, SCO1, SCOD1
Application Dilution: WB: 1:500~1:2000, IHC: 1:50~1:200
Specificity: SCO1 polyclonal antibody detects endogenous levels of SCO1 protein.
Immunogen:
Recombinant full length Human SCO1.
MW: ~ 34 kDa
Swis Prot.: O75880
Purification & Purity:
The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen and the purity is > 95% (by SDS-PAGE).
Format:
1mg/ml in PBS with 0.1% Sodium Azide, 50% Glycerol.
Storage:
Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze-thaw cycles.
For research use only, not for use in diagnostic procedure.
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