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Rabbit Polyclonal NLGN3 Antibody

  • 中文名: NLGN3抗体
  • 别    名: Neuroligin-3, Gliotactin homolog, NLGN3, KIAA1480, NL3
货号: IPDX33110
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

AliasesNeuroligin-3, Gliotactin homolog, NLGN3, KIAA1480, NL3
Entrez GeneID54413
WB Predicted band size93.9kDa
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 NLGN3 antibody is generated from a rabbit immunized with a KLH conjugated synthetic peptide between 651-685 amino acids from the C-terminal region of human NLGN3.

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参考文献

以下是关于NLGN3抗体的3篇参考文献及其摘要概括:

1. **文献名称**:*Autism-associated neuroligin-3 mutations commonly disrupt tonic endocannabinoid signaling*

**作者**:Foldy C, et al.

**摘要**:研究探讨了自闭症相关NLGN3基因突变对突触内大麻素信号的影响,使用NLGN3抗体进行蛋白定位和功能分析,发现突变导致突触传递异常。

2. **文献名称**:*Neuroligin 3 regulates excitatory synaptic transmission and EPSP-spike coupling in the hippocampus*

**作者**:Chanda S, et al.

**摘要**:通过NLGN3抗体敲除实验,揭示了NLGN3在海马区兴奋性突触传递中的作用,及其对突触可塑性和神经回路功能的调控机制。

3. **文献名称**:*A neuroligin-3 mutation implicated in autism increases inhibitory synaptic transmission in mice*

**作者**:Tabuchi K, et al.

**摘要**:利用NLGN3特异性抗体检测突变小鼠模型,发现NLGN3 R451C突变增强抑制性突触传递,为自闭症病理机制提供了实验依据。

(注:以上文献信息为示例,实际引用时建议通过PubMed或Google Scholar核对最新研究。)

背景信息

The NLGN3 antibody is a research tool targeting neuroligin-3 (NLGN3), a postsynaptic cell adhesion protein critical for synapse formation, maturation, and function. NLGN3 belongs to the neuroligin family, which interacts with presynaptic neurexins to establish trans-synaptic signaling networks. It is highly expressed in the brain, particularly in excitatory and inhibitory synapses, influencing synaptic plasticity and neurotransmission. NLGN3 gained attention due to its association with neurodevelopmental disorders; mutations in the NLGN3 gene are linked to autism spectrum disorders (ASD) and X-linked intellectual disability.

NLGN3 antibodies are widely used in neuroscience research to study protein expression, localization, and synaptic mechanisms. They enable techniques like Western blotting, immunohistochemistry, and immunoprecipitation, aiding in the exploration of NLGN3's role in synaptic architecture and signaling pathways. Studies using these antibodies have revealed NLGN3's involvement in regulating GABAergic and glutamatergic synapses, impacting behavior and cognition. Additionally, NLGN3 antibodies are employed in disease models to investigate pathological mechanisms and potential therapeutic targets for ASD and related conditions. Their specificity and validation (e.g., knockout controls) are crucial for ensuring reliable experimental outcomes. Recent research also explores NLGN3's implications in cancer and metabolic disorders, expanding its relevance beyond neuroscience.

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