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DNA pol γ2 Rabbit pAb

-YT1370

Catalog: YT1370
Size
Price
Status
Qty.
200μL
$450.00
In stock

0

100μL
$280.00
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40μL
$150.00
In stock

0

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Main Information
Target

DNA pol γ2

Host Species

Rabbit

Reactivity

Human, Mouse

Applications

IHC, IF, ELISA

MW

55kD (Calculated)

Conjugate/Modification


Unmodified

Detailed Information
Recommended Dilution Ratio
IHC 1:100-1:300; ELISA 1:20000; IF 1:50-200
Formulation
Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
Specificity
DNA pol γ2 Polyclonal Antibody detects endogenous levels of DNA pol γ2 protein.
Purification
The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Storage
-15°C to -25°C/1 year(Do not lower than -25°C)
Concentration
1 mg/ml
MW(Calculated)
55kD
Modification
Unmodified
Clonality
Polyclonal
Isotype
IgG
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Antigen&Target Information
Immunogen:
The antiserum was produced against synthesized peptide derived from human POLG2. AA range:291-340
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Specificity:
DNA pol γ2 Polyclonal Antibody detects endogenous levels of DNA pol γ2 protein.
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Gene Name:
POLG2
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Protein Name:
DNA polymerase subunit gamma-2 mitochondrial
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Other Name:
POLG2 ;
MTPOLB ;
DNA polymerase subunit gamma-2 ;
mitochondrial ;
DNA polymerase gamma accessory 55 kDa subunit ;
p55 ;
Mitochondrial DNA polymerase accessory subunit ;
MtPolB ;
PolG-beta
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Database Link:
Organism Gene ID SwissProt
Human 11232; Q9UHN1;
Mouse Q9QZM2;
Background:
This gene encodes the processivity subunit of the mitochondrial DNA polymerase gamma. The encoded protein forms a heterotrimer containing one catalytic subunit and two processivity subunits. This protein enhances DNA binding and promotes processive DNA synthesis. Mutations in this gene result in autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions.[provided by RefSeq, Sep 2009],
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Function:
Catalytic activity:Deoxynucleoside triphosphate + DNA(n) = diphosphate + DNA(n+1).,Disease:Defects in POLG2 are the cause of progressive external ophthalmoplegia with mitochondrial DNA deletions autosomal dominant type 4 (PEOA4) [MIM:610131]. Progressive external ophthalmoplegia is characterized by progressive weakness of ocular muscles and levator muscle of the upper eyelid. In a minority of cases, it is associated with skeletal myopathy, which predominantly involves axial or proximal muscles and which causes abnormal fatigability and even permanent muscle weakness. Ragged-red fibers and atrophy are found on muscle biopsy. A large proportion of chronic ophthalmoplegias are associated with other symptoms, leading to a multisystemic pattern of this disease. Additional symptoms are variable, and may include cataracts, hearing loss, sensory axonal neuropathy, ataxia, depression, hypogonadism, and parkinsonism.,Function:Mitochondrial polymerase processivity subunit. Stimulates the polymerase and exonuclease activities, and increases the processivity of the enzyme. Binds to ss-DNA.,subunit:Heterotrimer composed of a catalytic subunit and an homodimer of accessory subunits.,
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Cellular Localization:
Mitochondrion.
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Tissue Expression:
Cerebellum,Cervix,Ovary,
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Catalog: YT1370
Size
Price
Status
Qty.
200μL
$450.00
In stock

0

100μL
$280.00
In stock

0

40μL
$150.00
In stock

0

Add to cart

Collected

Collect

Customized Service

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