WB | 咨询技术 | Human,Mouse,Rat |
IF | 咨询技术 | Human,Mouse,Rat |
IHC | 1/100-1/500 | Human,Mouse,Rat |
ICC | 1/1000 | Human,Mouse,Rat |
FCM | 咨询技术 | Human,Mouse,Rat |
Elisa | 咨询技术 | Human,Mouse,Rat |
Aliases | Histone deacetylase 9, HD9, Histone deacetylase 7B, HD7, HD7b, Histone deacetylase-related protein, MEF2-interacting transcription repressor MITR, HDAC9, HDAC7, HDAC7B, HDRP, KIAA0744, MITR |
Entrez GeneID | 9734 |
WB Predicted band size | 111.3kDa |
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 |
Immunogen | This HDAC9 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 2-32 amino acids from the N-terminal region of human HDAC9. |
Formulation | Purified antibody in PBS with 0.05% sodium azide,1%BSA and 50% glycerol.prepared by Saturated Ammonium Sulfate (SAS) . |
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以下是关于HDAC9 (N-term)抗体的3篇参考文献示例(注:内容为模拟概括,建议核实实际文献):
1. **文献名称**:*"HDAC9 regulates macrophage polarization in atherosclerosis via N-terminal deacetylase activity"*
**作者**:Zhang Y, et al. (2016)
**摘要**:研究利用针对HDAC9 N端的特异性抗体,通过Western blot和免疫荧光验证其在巨噬细胞中的表达,发现HDAC9通过其N端结构域调控炎症基因的表观遗传修饰,影响动脉粥样硬化进程。
2. **文献名称**:*"The role of HDAC9 in cardiac hypertrophy: Insights from N-terminal domain-specific antibody targeting"*
**作者**:Wang L, et al. (2018)
**摘要**:作者开发了一种HDAC9 N端抗体,用于检测心肌细胞中HDAC9的亚细胞定位。研究发现,HDAC9的N端乙酰化状态通过结合转录因子MEF2.参与病理性心肌肥厚的调控。
3. **文献名称**:*"HDAC9 N-terminal antibody reveals isoform-specific functions in neuronal differentiation"*
**作者**:Müller S, et al. (2020)
**摘要**:通过使用HDAC9 N端特异性抗体,该研究揭示了HDAC9不同剪接变体在神经干细胞分化中的差异表达,并证明其N端结构域对神经元突触可塑性的关键作用。
如需真实文献,建议在PubMed或Google Scholar中检索关键词:**"HDAC9 antibody N-terminal"** 或 **"HDAC9 N-term epitope"**,筛选涉及抗体开发、验证或功能研究的文章。
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