Anti-SCO2 Antibody

$99.00$319.00

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

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Rabbit Anti-SCO2 Antibody (CSB-PA020853ESR2HU)

Supplier: CUSABIO BIOTECH CO.

Alternative names:

Protein SCO2 homolog Antibody,mitochondrial Antibody,SCO2 Antibody

More alternative names for the antibody
Cytochrome oxidase deficient homolog 2 antibody|MGC125823 antibody|MGC125825 antibody|OTTHUMP00000196774 antibody|OTTHUMP00000196775 antibody|Protein SCO2 homolog, mitochondrial antibody|SCO (cytochrome oxidase deficient, yeast) homolog 2 antibody|SCO 1L antibody|SCO 2 antibody|SCO cytochrome oxidase deficient homolog 2 (yeast) antibody|SCO cytochrome oxidase deficient homolog 2 antibody|SCO1L antibody|SCO2 antibody|SCO2_HUMAN antibody|Synthesis of cytochrome c oxidase 2 antibody
Anti-SCO2 antibody (ab115877)
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Recommended applications: ELISA, IHC

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

Recommended protocols: check protocols

Name

Anti-SCO2 Antibody

Catalogue No.

CSB-PA020853ESR2HU

Reactivity

Human

Immunogen

Recombinant human Protein SCO2 homolog, mitochondrial protein (1-130AA)

Host

Rabbit

Applications

ELISA, IHC

Recommended dilution

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

Clonality

Polyclonal

Conjugation

unconjugated

Isotype

IgG

Molecular weight

29 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:9997( Human), Omim:604272( Human), SwissProt:O43819( Human), Unigene:180903( Human), Unigene:592212( Human)

Protein function

Acts as a copper chaperone, transporting copper to the Cu(A) site on the cytochrome c oxidase subunit II (COX2).

Protein tissue specificity

Ubiquitous.

Involvement in disease

Cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 1 (CEMCOX1) [MIM:604377]: A disorder characterized by hypotonia, developmental delay, hypertrophic cardiomyopathy, lactic acidosis, gliosis, neuronal loss in basal ganglia, brainstem and spinal cord, and cytochrome c oxidase deficiency. . Note=The disease is caused by mutations affecting the gene represented in this entry.; Myopia 6 (MYP6) [MIM:608908]: A refractive error of the eye, in which parallel rays from a distant object come to focus in front of the retina, vision being better for near objects than for far. . 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 may be caused by mutations affecting the gene represented in this entry.

Protein sequence and domain

Belongs to the SCO1/2 family.

Protein cellular localization

Mitochondrion.

Research area

All research areas>Transport and Trafficking>SCO1 and SCO2
(View all antibody categories related to Transport and Trafficking)

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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