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Rabbit Polyclonal AHI1 Antibody

  • 中文名: AHI1抗体
  • 别    名: Jouberin, Abelson helper integration site 1 protein homolog, AHI-1, AHI1
货号: IPDX33359
Price: ¥1180
数量:
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验证与应用

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

产品详情

AliasesJouberin, Abelson helper integration site 1 protein homolog, AHI-1, AHI1
Entrez GeneID54806
WB Predicted band size137.1kDa
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
ImmunogenThis AHI1 antibody is generated from a rabbit immunized with a KLH conjugated synthetic peptide between 389-422 amino acids from the Central region of human AHI1.

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参考文献

以下是关于AHI1抗体的3篇参考文献示例(文献信息为模拟内容,实际引用请核对真实文献):

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1. **文献名称**:*AHI1 mutations cause Joubert syndrome with cortical polymicrogyria through impaired neuronal ciliogenesis*

**作者**:Dixon-Salazar TJ, et al.

**摘要**:该研究通过免疫荧光和Western blot技术,利用AHI1特异性抗体揭示了AHI1蛋白在小脑神经元纤毛形成中的关键作用,并发现其突变导致Joubert综合征患者皮层多微脑回畸形的分子机制。

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2. **文献名称**:*The Joubert syndrome-associated protein AHI1 interacts with the cytoplasmic dynein motor complex*

**作者**:Louie CM, et al.

**摘要**:研究通过免疫共沉淀(Co-IP)结合AHI1抗体,发现AHI1与细胞质动力蛋白复合物的相互作用,揭示了其在神经元内运输和纤毛信号传导中的功能,为理解Joubert综合征的病理机制提供了实验依据。

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3. **文献名称**:*AHI1 localizes to the photoreceptor cilium and interacts with RPGRIP1: implications for retinal degeneration*

**作者**:Ferland RJ, et al.

**摘要**:利用AHI1抗体进行免疫组织化学分析,证实AHI1在视网膜感光细胞纤毛中的定位,并发现其与RPGRIP1的相互作用异常可能导致纤毛功能障碍,进而引发视网膜变性相关疾病。

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**注**:以上文献信息为示例,实际研究中建议通过PubMed或Google Scholar以“AHI1 antibody”或“AHI1 protein function”为关键词检索最新文献,重点关注其实验方法中对抗体的具体应用(如定位、表达调控或互作研究)。

背景信息

The AHI1 (Abelson helper integration site 1) antibody is a tool used to study the AHI1 protein, encoded by the *AHI1* gene, which plays a critical role in neuronal and ciliary function. AHI1. also known as Jouberin, is predominantly expressed in the brain, particularly in cerebellar neurons and retinal photoreceptors. It contributes to ciliogenesis, intracellular trafficking, and synaptic connectivity, with implications for neurodevelopment. Mutations in *AHI1* are linked to Joubert syndrome, a rare autosomal recessive disorder characterized by cerebellar hypoplasia, developmental delays, and retinal degeneration. The AHI1 antibody aids in detecting protein expression, localization, and interaction partners in cellular and tissue models, helping elucidate its role in ciliary signaling pathways and neuronal maintenance. Research also explores its potential involvement in cancer, as altered AHI1 expression has been observed in certain tumors. However, its precise mechanisms in oncogenesis remain unclear. The antibody is widely used in techniques like Western blotting, immunohistochemistry, and immunofluorescence, supporting studies on neurodevelopmental disorders and ciliopathies. Understanding AHI1's function through antibody-based assays provides insights into disease pathogenesis and therapeutic targets.

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