Anti-COX10 Antibody

$99.00$319.00

Reactivity: Human
Applications: ELISA,IHC
Conjugation: Various
Supplier: CUSABIO BIOTECH CO.

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Rabbit Anti-COX10 Antibody (CSB-PA621520ESR2HU)

Supplier: CUSABIO BIOTECH CO.

Alternative names:

Protoheme IX farnesyltransferase Antibody,mitochondrial Antibody,Heme O synthase Antibody,COX10 Antibody

More alternative names for the antibody
2410004F01Rik antibody|AU042636 antibody|COX10 antibody|COX10_HUMAN antibody|Cytochrome c oxidase assembly protein antibody|Cytochrome c oxidase subunit X antibody|Heme A farnesyltransferase antibody|Heme O synthase antibody|OTTMUSP00000006085 antibody|Protoheme IX farnesyltransferase, mitochondrial antibody|Protoheme IX farnesyltransferase, mitochondrial precursor antibody|RP23-78H18.1 antibody
Anti-COX10 antibody (ab84053)
Close sc-134792|

Recommended applications: ELISA, IHC

Recommended dilution: Recommended dilution:IHC:1:20-1:200

Recommended protocols: check protocols

Name

Anti-COX10 Antibody

Catalogue No.

CSB-PA621520ESR2HU

Reactivity

Human

Immunogen

Recombinant human Protoheme IX farnesyltransferase, mitochondrial protein (1-160AA)

Host

Rabbit

Applications

ELISA, IHC

Recommended dilution

Recommended dilution:IHC:1:20-1:200

Clonality

Polyclonal

Conjugation

unconjugated

Isotype

IgG

Molecular weight

48 kDa

Purification

Antigen Affinity Purified

Storage

Shipped at 4 Celcius Degree. Upon delivery aliquot and store at -20 Celcius Degree or -80 Celcius Degree. Avoid repeated freeze.

Database links

Entrez Gene:417329( Chicken), Entrez Gene:511440( Cow), Entrez Gene:100073118( Horse), Entrez Gene:1352( Human), Entrez Gene:70383( Mouse), Entrez Gene:363617( Rat), Entrez Gene:553384 ( Zebrafish), Omim:602125( Human), SwissProt:Q12887( Human), SwissProt:Q8CFY5( Mouse), Unigene:462278( Human), Unigene:340211( Mouse)

Protein function

Converts protoheme IX and farnesyl diphosphate to heme O. .

Involvement in disease

Mitochondrial complex IV deficiency (MT-C4D) [MIM:220110]: 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, exercise intolerance, developmental delay, delayed motor development and mental retardation. Some affected individuals manifest a fatal hypertrophic cardiomyopathy resulting in neonatal death. A subset of patients manifest Leigh syndrome. . Note=The disease is caused by mutations affecting the gene represented in this entry.; Leigh syndrome (LS) [MIM:256000]: An early-onset progressive neurodegenerative disorder characterized by the presence of focal, bilateral lesions in one or more areas of the central nervous system including the brainstem, thalamus, basal ganglia, cerebellum and spinal cord. Clinical features depend on which areas of the central nervous system are involved and include subacute onset of psychomotor retardation, hypotonia, ataxia, weakness, vision loss, eye movement abnormalities, seizures, and dysphagia. Note=The disease is caused by mutations affecting the gene represented in this entry.

Protein sequence and domain

Belongs to the UbiA prenyltransferase family.

Protein cellular localization

Mitochondrion membrane; Multi-pass membrane protein.

Research area

All research areas>Synthesis and Degradation>Cytochrome c Oxidase
(View all antibody categories related to Synthesis and Degradation)

Note

AntibodyPlus provides antibody trial sample for your own antibody validation and collects antibody reviews.

Supplier

CUSABIO BIOTECH CO.

Product type

Primary antibody

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