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Rabbit Polyclonal TIMM8A Antibody

  • 中文名: TIMM8A抗体
  • 别    名: DDP; MTS; DDP1; DFN1; TIM8
货号: IPDX09802
Price: ¥1180
数量:
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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 1/40-1/200 Human,Mouse,Rat
ICC 技术咨询 Human,Mouse,Rat
FCM 咨询技术 Human,Mouse,Rat
Elisa 1/5000-1/10000 Human,Mouse,Rat

产品详情

AliasesDDP; MTS; DDP1; DFN1; TIM8
Host/IsotypeRabbit IgG
Antibody TypePrimary antibody
StorageStore at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze/thaw cycles.
Species ReactivityHuman, Mouse, Rat
ImmunogenFusion protein of human TIMM8A
FormulationPurified antibody in PBS with 0.05% sodium azide and 50% glycerol.

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参考文献

以下是关于TIMM8A抗体的3篇参考文献及其摘要概述:

1. **文献名称**: "Mutations in the mitochondrial Tim8a gene promote neurodegeneration in mice by inducing oxidative stress"

**作者**: Roesch, K., et al.

**摘要概述**: 该研究通过使用TIMM8A特异性抗体进行免疫印迹分析,发现TIMM8A基因突变导致小鼠线粒体功能异常,引发氧化应激和神经元退行性病变,与人类Mohr-Tranebjaerg综合征的病理机制相关。

2. **文献名称**: "Characterization of the human TIMM8A and TIMM8B genes in mitochondrial disorders"

**作者**: Jin, H., et al.

**摘要概述**: 作者利用TIMM8A抗体进行免疫荧光定位,证实TIMM8A蛋白主要定位于线粒体内膜,并揭示其在蛋白质转运复合体中的相互作用。研究还发现TIMM8A表达缺失与X-linked耳聋-肌张力障碍综合征相关。

3. **文献名称**: "Proteomic analysis of mitochondrial carriers using TIMM8A-specific antibodies reveals its role in metabolic regulation"

**作者**: Smith, T.J., & Johnson, A.E.

**摘要概述**: 通过TIMM8A抗体富集线粒体膜蛋白复合物,结合质谱分析,发现TIMM8A与其他转运蛋白(如TIMM13)形成复合物,参与小分子代谢物运输,并影响细胞能量代谢稳态。

(注:以上文献信息为基于领域相关研究的示例性概括,实际引用需以具体文献为准。)

背景信息

The TIMM8A antibody is a tool used to detect TIMM8A (Translocase of Inner Mitochondrial Membrane 8 Homolog A), a protein critical for mitochondrial function. TIMM8A, also known as DDP1. is part of the mitochondrial TIM8-TIM13 complex, which facilitates the import and assembly of membrane proteins, particularly in the inner mitochondrial membrane. This protein plays a role in the transport of hydrophobic substrates like TIM22 complex components, essential for maintaining mitochondrial membrane potential and energy production.

Mutations in the TIMM8A gene are linked to Mohr-Tranebjaerg syndrome, an X-linked recessive disorder characterized by neurodegeneration, sensorineural hearing loss, and dystonia. Research using TIMM8A antibodies has helped elucidate its expression patterns, subcellular localization, and interaction partners, aiding in understanding mitochondrial dysfunction in disease contexts. These antibodies are widely employed in techniques such as Western blotting, immunohistochemistry, and immunofluorescence to study TIMM8A's role in cellular health, neurodegeneration, and metabolic disorders. Recent studies also explore its potential involvement in cancer and aging, highlighting its broader biological significance.

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