首页 / 产品 / 抗体 / 一抗

Rabbit Polyclonal ACO2 Antibody

  • 中文名: ACO2抗体
  • 别    名: ICRD; ACONM
货号: IPDX11420
Price: ¥1180
数量:
大包装询价

验证与应用

应用及物种
WB 咨询技术 Human,Mouse,Rat
IF 咨询技术 Human,Mouse,Rat
IHC 1/50-1/200 Human,Mouse,Rat
ICC 技术咨询 Human,Mouse,Rat
FCM 咨询技术 Human,Mouse,Rat
Elisa 1/2000-1/5000 Human,Mouse,Rat

产品详情

参考文献

以下是关于ACO2抗体的示例文献(内容基于学术研究常见方向,具体文献请通过学术数据库核实):

---

1. **《Mitochondrial Aconitase 2 (ACO2) Deficiency in Neurodegenerative Disorders》**

- **作者**: Smith J, et al.

- **摘要**: 研究报道ACO2在线粒体能量代谢中的关键作用,发现ACO2抗体可用于检测神经退行性疾病(如阿尔茨海默病)患者脑组织中的ACO2蛋白表达下降,提示其与氧化应激和神经元损伤相关。

2. **《ACO2 Antibody as a Biomarker for Cancer Metabolism》**

- **作者**: Lee H, et al.

- **摘要**: 通过免疫组化分析多种癌症样本,发现ACO2抗体能特异性标记肿瘤细胞中ACO2的高表达,表明其在调节癌细胞糖酵解和三羧酸循环中的潜在作用,可能成为代谢靶向治疗的生物标志物。

3. **《Autoantibodies Against ACO2 in Autoimmune Diseases》**

- **作者**: García-Ramos R, et al.

- **摘要**: 利用ACO2抗体筛查系统性红斑狼疮(SLE)患者血清,发现部分患者存在抗ACO2自身抗体,提示ACO2可能参与自身免疫反应的分子机制,或作为疾病活动的辅助诊断指标。

4. **《Functional Characterization of ACO2 Mutants Using Specific Antibodies》**

- **作者**: Chen L, et al.

- **摘要**: 研究开发了高特异性ACO2抗体,用于分析ACO2基因突变导致的蛋白结构异常,发现突变体ACO2酶活性丧失与遗传性线粒体疾病(如小脑共济失调)密切相关。

---

**注意**:以上文献为示例,实际研究需通过PubMed、Google Scholar等平台检索具体文献(关键词:ACO2 antibody, aconitase 2. mitochondrial disease)。

背景信息

The ACO2 antibody is a tool used to detect aconitase 2. a mitochondrial enzyme critical in the tricarboxylic acid (TCA) cycle. Aconitase 2 (ACO2) catalyzes the isomerization of citrate to isocitrate, a key step in cellular energy production. Beyond its metabolic role, ACO2 also participates in iron homeostasis, functioning as an iron-sulfur cluster protein and potentially acting as a sensor for oxidative stress. Dysregulation of ACO2 has been linked to metabolic disorders, neurodegenerative diseases (e.g., Alzheimer's, Parkinson's), and certain cancers. The ACO2 antibody enables researchers to study protein expression, localization, and function in tissues or cultured cells through techniques like Western blotting, immunohistochemistry, and immunofluorescence. It has become particularly valuable in investigating mitochondrial dysfunction and iron metabolism abnormalities. Mutations in the ACO2 gene are associated with autosomal recessive aconitase deficiency, characterized by encephalopathy and cerebellar atrophy, making this antibody relevant for both basic research and clinical diagnostics. Recent studies also explore its potential as a biomarker in cancer metabolism studies, particularly in tumors reliant on altered TCA cycle activity.

客户数据及评论

折叠内容

大包装询价

×