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COX10 Rabbit anti-Human, Mouse, Rat, Polyclonal, Proteintech
SDP

Rabbit Polyclonal Antibody

Supplier:  Proteintech Group Inc 106112AP150UL

Encompass_Preferred

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Catalog No. 50-172-6447


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Description

Description

Defects in COX10 are a cause of mitochondrial complex IV deficiency (MT-C4D); also known as cytochrome c oxidase deficiency. A disorder of the mitochondrial respiratory chain with heterogeneous clinical manifestations, ranging from isolated myopathy to severe multisystem disease affecting several tissues and organs. Features include hypertrophic cardiomyopathy, hepatomegaly and liver dysfunction, hypotonia, muscle weakness, excercise intolerance, developmental delay, delayed motor development and mental retardation. A subset of patients manifest Leigh syndrome.
Specifications

Specifications

COX10
Polyclonal
Unconjugated
COX10
COX10, Heme O synthase
Rabbit
Antigen Affinity Chromatography
RUO
1352, 691853, 70383
-20°C
Liquid
Western Blot
0.33 mg/mL
PBS with 50% glycerol and 0.1% sodium azide; pH 7.3
Q12887, Q8CFY5
Cox10
COX10 Fusion Protein Ag0930
150 μL
Primary
Human, Mouse, Rat
Antibody
IgG
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