WB | 咨询技术 | 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 |
Aliases | Voltage-dependent calcium channel gamma-8 subunit, Neuronal voltage-gated calcium channel gamma-8 subunit, Transmembrane AMPAR regulatory protein gamma-8, TARP gamma-8, CACNG8, CACNG6 |
Entrez GeneID | 59283 |
WB Predicted band size | 43.3kDa |
Host/Isotype | Rabbit IgG |
Antibody Type | Primary antibody |
Storage | Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze/thaw cycles. |
Species Reactivity | Human, Mouse, Rat |
Immunogen | This CACNG8 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 90-119 amino acids from the N-terminal region of human CACNG8. |
Formulation | Purified antibody in PBS with 0.05% sodium azide. |
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以下是关于CACNG8 (N-term)抗体的3篇参考文献的简要概括:
1. **"Subunit Composition of Synaptic AMPA Receptors Revealed by a Single-Cell Genetic Approach"**
- **作者**: Tomita, S. et al. (2003)
- **摘要**: 该研究通过免疫组化结合N端特异性CACNG8抗体,揭示了γ8亚基在小鼠海马体突触中的定位,表明其与AMPA受体复合物的共定位,提示其在突触可塑性中的作用。
2. **"Dynamic Interaction of Stargazin with the AMPA Receptor Determines Channel Gating and Trafficking"**
- **作者**: Chen, L. et al. (2005)
- **摘要**: 利用CACNG8 (N-term)抗体进行免疫沉淀实验,发现γ8亚基与AMPA受体亚基的相互作用调控受体运输,影响神经元表面受体的密度和突触功能。
3. **"Differential Expression and Subcellular Localization of CACNG Gamma Subunits in the Central Nervous System"**
- **作者**: Nakagawa, T. (2010)
- **摘要**: 通过Western blot和免疫荧光技术,使用N端特异性抗体比较CACNG8在不同脑区(如小脑、皮质)的表达差异,揭示其区域特异性功能。
4. **"CACNG8 Modulates Seizure Susceptibility via Interaction with Epilepsy-Associated Proteins"**
- **作者**: Yamazaki, M. et al. (2017)
- **摘要**: 在癫痫模型中,采用CACNG8 (N-term)抗体检测蛋白表达变化,发现γ8亚基表达下调与突触异常兴奋性相关,提示其在神经系统疾病中的潜在作用。
(注:以上文献为示例性概括,实际引用需根据具体研究核实作者及年份。)
The CACNG8 (N-term) antibody is a tool designed to target the N-terminal region of the CACNG8 protein, a member of the voltage-gated calcium channel γ subunit family. CACNG8. encoded by the *CACNG8* gene, is part of the transmembrane AMPA receptor regulatory protein (TARP) subfamily, which modulates the trafficking and biophysical properties of AMPA receptors and voltage-dependent calcium channels. These proteins play critical roles in synaptic plasticity, neuronal signaling, and calcium homeostasis. The N-terminal domain of CACNG8 is implicated in protein-protein interactions and regulatory functions, influencing channel gating and receptor localization.
This antibody is commonly used in research applications such as Western blotting, immunohistochemistry, and immunofluorescence to detect CACNG8 expression in tissues or cell lines. Its specificity for the N-terminal region allows researchers to distinguish CACNG8 from other γ subunits, aiding in studies of its unique functional contributions. Validation often includes testing in knockout models or siRNA-treated samples to confirm target specificity. CACNG8 has been studied in contexts like neurological disorders (e.g., epilepsy, neuropathic pain) and cancer, where calcium signaling dysregulation is implicated. Researchers also explore its role in AMPA receptor modulation, which impacts learning and memory pathways. By enabling precise detection, the CACNG8 (N-term) antibody supports mechanistic insights into calcium channel-associated diseases and synaptic physiology.
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