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首页 > 产品中心 > 抗体系列 > 一抗

货号:BSCY0048

SOD2 Rabbit mAb

SOD2;Superoxide dismutase [Mn], mitochondrial

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别名 SOD2;Superoxide dismutase [Mn], mitochondrial
基因名称 SOD2
蛋白名称 Superoxide dismutase [Mn] mitochondrial
推荐应用
反应物种 Human,Mouse,Rat,
存储缓冲液 PBS, 50% glycerol, 0.05% Proclin 300, 0.05%BSA
Human Gene Link 6648
Human Swissprot No. P04179
Mouse Gene ID 20656
Mouse Swissprot No. P09671
Rat Gene ID 24787
Rat Swissprot No. P07895
特异性 endogenous
稀释度 IHC 1:200-1:1000;WB 1:1000-1:2500;IF 1:200-1:1000;ELISA 1:5000-1:20000;IP 1:50-1:200,
参考分子量 MW(Observed):22kD
预测分子量 MW(Calculated):25kD
运输及保存条件 -15°C to -25°C/1 year(Do not lower than -25°C)
宿主 Rabbit
同种型 IgG,Kappa
背景介绍 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],
细胞定位 Mitochondrion matrix
功能 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.,
纯化 Protein A
Clonality Monoclonal
修饰类型 Unmodified
细胞定位 Mitochondrion matrix
组织表达 Brain,Colon,Heart,Liver,Lung,Mammary carcinoma,Tongue,
研究领域 >>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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