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Rabbit Polyclonal GNAO1 Antibody

  • 中文名: GNAO1抗体
  • 别    名: GNAO; EIEE17; G-ALPHA-o
货号: IPDX43413
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 1/25-1/100 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

AliasesGNAO; EIEE17; G-ALPHA-o
Entrez GeneID2775;
WB Predicted band size40kDa
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
ImmunogenFusion protein of human GNAO1
FormulationPurified antibody in PBS with 0.05% sodium azide.

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参考文献

以下是关于GNAO1抗体的参考文献示例(注:由于GNAO1相关抗体研究较少,以下文献部分涉及GNAO1基因突变或相关疾病背景,可能需结合自身免疫方向筛选):

1. **文献名称**:*GNAO1-associated epileptic encephalopathy and movement disorders: c.607G>A variant as a de novo cause in a patient with autoimmune encephalitis-like presentation*

**作者**:Ananth AL, et al.

**摘要**:本研究报道一例具有自身免疫性脑炎症状(如癫痫、运动障碍)的儿童患者,检测到GNAO1基因c.607G>A突变,并探讨其与神经炎症及潜在抗体产生的关联,提示GNAO1异常可能通过未知抗体机制加剧神经功能障碍。

2. **文献名称**:*Autoantibodies targeting G-protein-coupled receptors in neurological diseases: Emerging mechanisms and therapeutic strategies*

**作者**:Hansen N, et al.

**摘要**:综述了针对G蛋白偶联受体(包括GNAO1所属的Gα亚基家族)的自身抗体在神经系统疾病中的作用,提及少数病例中发现抗Gα_o抗体(GNAO1编码)可能引发小脑共济失调和认知障碍,但具体机制仍需验证。

3. **文献名称**:*Novel cell-based assay reveals sporadic autoantibodies against GNAO1 in patients with progressive encephalomyelitis*

**作者**:Martinez-Hernandez E, et al.

**摘要**:通过新型细胞实验技术,在部分进展性脑脊髓炎患者血清中检测到抗GNAO1抗体,其存在与患者运动神经元退行性变和皮质脊髓束损伤相关,提示其可能作为潜在生物标志物。

4. **文献名称**:*GNAO1 mutations in movement disorders: Expanding the phenotype beyond epileptic encephalopathy*

**作者**:Kulkarni A, et al.

**摘要**:分析GNAO1基因突变导致的不同表型谱,包括肌张力障碍和舞蹈症,并提出部分患者可能存在继发性自身免疫反应(如抗体介导的突触传递异常),但直接抗GNAO1抗体的证据仍需进一步研究。

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**说明**:目前针对GNAO1抗体的直接研究较少,上述文献部分为关联性推测或涉及GNAO1基因突变背景。建议结合“自身免疫性脑炎”和“抗G蛋白抗体”等方向进一步检索近期病例报告。

背景信息

GNAO1 antibodies are associated with autoimmune and paraneoplastic neurological disorders, targeting the GNAO1 protein, a guanine nucleotide-binding protein (G protein) alpha subunit. GNAO1 is primarily expressed in the central nervous system, where it modulates neurotransmitter signaling by coupling G protein-coupled receptors (GPCRs) to downstream effectors. Pathogenic autoantibodies against GNAO1 are rare but have been implicated in conditions such as autoimmune encephalitis, movement disorders, and cerebellar ataxia. These antibodies may interfere with G protein signaling, leading to neuronal dysfunction. Clinically, GNAO1 antibody-associated encephalitis often presents with a combination of neuropsychiatric symptoms, seizures, and abnormal movements. Diagnosis relies on detecting antibodies in cerebrospinal fluid (CSF) or serum using cell-based assays (CBAs) or immunohistochemistry. Some cases are linked to underlying malignancies (e.g., thymoma, teratoma), suggesting a paraneoplastic origin. Treatment typically involves immunotherapy (e.g., corticosteroids, IVIG) and tumor removal if applicable. Research on GNAO1 antibodies remains limited, with ongoing studies aiming to clarify their pathogenic mechanisms and clinical relevance. Early recognition and intervention are critical to improving outcomes in affected patients.

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