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SOD2 (PTR1396) Mouse mAb

-YM4265

Catalog: YM4265
Size
Price
Status
Qty.
200μL
$600.00
3 weeks

0

100μL
$340.00
3 weeks

0

40μL
$190.00
3 weeks

0

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Collected

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Main Information
Target

SOD2

Host Species

Mouse

Reactivity

Human, Mouse, Rat,

Applications

WB, IF, ELISA

MW

25kD (Calculated)

25kD (Observed)

Conjugate/Modification


Unmodified

Detailed Information
Recommended Dilution Ratio
WB 1:500-2000; IF 1:100-500; ELISA 1:1000-5000;
Formulation
PBS, 50% glycerol, 0.05% Proclin 300, 0.05%BSA
Specificity
This antibody detects endogenous levels of SOD2 protein.
Purification
The antibody was affinity-purified from ascites by affinity-chromatography using specific immunogen.
Storage
-15°C to -25°C/1 year(Do not lower than -25°C)
MW(Calculated)
25kD
MW(Observed)
25kD
Modification
Unmodified
Clonality
Monoclonal
Clone Number
PTR1396
Related Products
Primary Antibodies
SOD-2 Rabbit pAb
YT5575

More→

Proteins
SOD2 protein
YD0095

More→

Antigen&Target Information
Immunogen:
AA range: 1-222
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Specificity:
This antibody detects endogenous levels of SOD2 protein.
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Gene Name:
SOD2
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Protein Name:
Superoxide dismutase [Mn] mitochondrial
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Other Name:
SOD2 ;
Superoxide dismutase [Mn], mitochondrial
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Database Link:
Organism Gene ID SwissProt
Human 6648; P04179;
Mouse 20656; P09671;
Rat 24787; P07895;
Background:
This gene is a member of the iron/manganese superoxide dismutase family. It encodes a mitochondrial protein that forms a homotetramer and binds one manganese ion per subunit. This protein binds to the superoxide byproducts of oxidative phosphorylation and converts them to hydrogen peroxide and diatomic oxygen. Mutations in this gene have been associated with idiopathic cardiomyopathy (IDC), premature aging, sporadic motor neuron disease, and cancer. Alternative splicing of this gene results in multiple transcript variants. A related pseudogene has been identified on chromosome 1. [provided by RefSeq, Apr 2016],
Function:
Catalytic activity:2 superoxide + 2 H(+) = O(2) + H(2)O(2).,cofactor:Binds 1 manganese ion per subunit.,Disease:Genetic variation in SOD2 is associated with susceptibility to diabetic nephropathy [MIM:612634]; also called susceptibility to microvascular complications of diabetes type 6 (MVCD6). Diabetic nephropathy is a kidney disease and resultant kidney function impairment due to the long standing effects of diabetes on the microvasculature (glomerulus) of the kidney. Features include increased urine protein and declining kidney function.,Function:Destroys radicals which are normally produced within the cells and which are toxic to biological systems.,online information:Superoxide dismutase entry,online information:The Singapore human mutation and polymorphism database,PTM:Nitrated under oxidative stress. Nitration coupled with oxidation inhibits the catalytic activity.,similarity:Belongs to the iron/manganese superoxide dismutase family.,subunit:Homotetramer.,
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Cellular Localization:
Mitochondrion matrix
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Tissue Expression:
Brain,Colon,Heart,Liver,Lung,Mammary carcinoma,Tongue,
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Research Areas:
>>FoxO signaling pathway ;
>>Peroxisome ;
>>Longevity regulating pathway ;
>>Longevity regulating pathway - multiple species ;
>>Huntington disease ;
>>Chemical carcinogenesis - reactive oxygen species ;
>>Lipid and atherosclerosis
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Catalog: YM4265
Size
Price
Status
Qty.
200μL
$600.00
3 weeks

0

100μL
$340.00
3 weeks

0

40μL
$190.00
3 weeks

0

Add to cart

Collected

Collect

Customized Service

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