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Anti-SOD1 Antibody-PE (8C907)
还可以产品编号 TMAY-02022P
Anti-SOD1 Antibody-PE (8C907) 是一种 PE-conjugated Mouse 抗体，靶向 SOD1。Anti-SOD1 Antibody-PE (8C907) 可用于 FCM。
Anti-SOD1 Antibody-PE (8C907)
Anti-SOD1 Antibody-PE (8C907)
还可以产品编号 TMAY-02022P
Anti-SOD1 Antibody-PE (8C907) 是一种 PE-conjugated Mouse 抗体，靶向 SOD1。Anti-SOD1 Antibody-PE (8C907) 可用于 FCM。
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产品介绍
生物活性
偶联与修饰
抗原信息
| 产品描述 | Anti-SOD1 Antibody-PE (8C907) is a PE-conjugated Mouse antibody targeting SOD1. Anti-SOD1 Antibody-PE (8C907) can be used in FCM. |
| Ig Type | Monoclonal Mouse IgG2b |
| 克隆号 | 8C907 |
| 交叉反应 | Human |
| 验证活性 | Flow cytometric analysis of Human SOD1 expression in HeLa cells. |
| 应用 | FCM |
| 推荐剂量 | 5 μl/Test, 0.1 mg/ml |
| 抗体种类 | Monoclonal |
| 宿主来源 | Mouse |
| 构建方式 | This antibody was produced from a hybridoma resulting from the fusion of a mouse myeloma with B cells obtained from a mouse immunized with purified, recombinant Human SOD1 (rh SOD1; TMPY-01585; NP_000445.1; Ala2-Gln154) and conjugated with PE under optimum conditions, the unreacted PE was removed. |
| 纯化方式 | Protein A |
| 性状 | Liquid |
| 缓冲液 | PBS solution containing 0.5% BSA and 0.09% sodium azide |
| 研究背景 | SOD1 belongs to the Cu-Zn superoxide dismutase family. It binds copper and zinc ions and is one of two isozymes responsible for destroying free superoxide radicals in the body. The encoded isozyme is a soluble cytoplasmic protein, acting as a homodimer to convert naturally-occuring but harmful superoxide radicals to molecular oxygen and hydrogen peroxide. The other isozyme is a mitochondrial protein. Mutations in this gene have been implicated as causes of familial amyotrophic lateral sclerosis. Rare transcript variants have been reported for this gene. SOD1 destroys radicals which are normally produced within the cells and which are toxic to biological systems. Defects in SOD1 are the cause of amyotrophic lateral sclerosis type 1 (ALS1). ALS1 is a familial form of amyotrophic lateral sclerosis, a neurodegenerative disorder affecting upper and lower motor neurons and resulting in fatal paralysis. Sensory abnormalities are absent. Death usually occurs within 2 to 5 years. The etiology of amyotrophic lateral sclerosis is likely to be multifactorial, involving both genetic and environmental factors. The disease is inherited in 5-10% of cases leading to familial forms. |
| 偶联 | PE |
| 其他可选修饰符 | Unconjugated/FITC |
| 可提供抗体种类 | 3 |
| 免疫原 | Recombinant Human SOD1 protein (TMPY-01585) |
| 抗原种属 | Human |
存储&运输
| 储存方式 | Store at 2°C-8°C for 12 months, do not freeze. Keep away from direct sunlight. Sodium azide is toxic to cells and should be disposed of properly. Flush with large volumes of water during disposal. |
| 运输方式 | Shipping with blue ice. |
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比如您的给药剂量是 10 mg/kg ，每只动物体重 20 g ，给药体积 100 μL ， 
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