MAP2 Polyclonal antibody (17490-1-AP)
MAP 2; MAP-2; MAP2A; MAP2B; MAP2C
用户验证的应用
经验证应用
| 项目 | 详情 |
|---|---|
| Positive WB detected in | SH-SY5Y cells, rat brain tissue, mouse brain tissue |
| Positive IP detected in | mouse brain tissue |
| Positive IHC detected in | mouse brain tissue Note: suggested antigen retrieval with TE buffer pH 9.0; (*) Alternatively, antigen retrieval may be performed with citrate buffer pH 6.0 |
| Positive IF-P detected in | rat brain tissue, mouse brain tissue |
| Positive IF-Fro detected in | mouse brain tissue, rat brain tissue |
| Positive IF/ICC detected in | iPS cells |
| Positive FC (Intra) detected in | Neuro-2a cells |
推荐稀释说明
It is recommended that this reagent should be titrated in each testing system to obtain optimal results. Sample-dependent, Check data in validation data gallery.
详细信息
背景信息
Microtubule-associated protein 2 (MAP2) is a tubulin binding protein regulating the spacing and stability of microtubules and contributing to elongation of dendrites. What is the molecular weight of MAP2? Is MAP2 post-translationally modified? MAP2 has multiple isoforms that arise from alternative splicing (PMID: 3121794, 7854050, and 10383434). They are classified into two groups - MAP2A and MAP2B, which are known as high molecular weight (HMW) isoforms, run as ~280 kDa species, while low molecular weight (LMW) isoforms MAP2C and MAP2D are around ~70 kDa. MAP2 proteins are heavily phosphorylated, which contributes to a large discrepancy between their predicted and observed molecular weight in SDS-PAGE (220 vs 280 kDa for HMW forms). What is the tissue expression pattern of MAP2? What is the subcellular localization of MAP2? MAP2 isoforms differ in their tissue and developmental expression pattern (PMID: 2469170 and 3898077). In the brain, MAP2B is widely expressed during and post development, MAP2A is expressed postnatally, while MAP2C is present only in the early development except of present in photosensitive cells of the adult retina and in the olfactory system. MAP proteins are highly expressed in the CNS found in cell bodies and dendrites of neurons, in dorsal root ganglion, reactive glia, and in the testis (PMID: 9588626). In neurons, MAP2 proteins are found in the cell body and dendrites, where they associate with microtubules, while they can also be present in the nuclei of testicular cells. Can MAP2 be used as a neuronal marker? MAP2 proteins are abundantly expressed in neurons. MAP2 is frequently used as a dendritic marker because it is present in the cell body and dendrites of neurons but absent in axons (PMID: 28413822).
文献引用 (138)
Pathological axonal enlargement in connection with amyloidosis, lysosome destabilization, and bleeding is a major defect in Alzheimer's disease.
病理性轴突增大与淀粉样变性、溶酶体不稳定和出血有关,是阿尔茨海默病的主要缺陷
Charting the spatial transcriptome of the human cerebral cortex at single-cell resolution.
以单细胞分辨率绘制人类大脑皮层的空间转录组图
Repair-associated macrophages increase after early-phase microglia attenuation to promote ischemic stroke recovery
早期小胶质细胞减少后,修复相关巨噬细胞数量增加,从而促进缺血性卒中后的恢复。
Neuronal FGF13 Inhibits Mitochondria-Derived Damage Signals to Prevent Neuroinflammation and Neurodegeneration in a Mouse Model of Parkinson's Disease.
神经元 FGF13 抑制线粒体衍生的损伤信号,从而预防帕金森病小鼠模型中的神经炎症和神经退行性变
Microglia Process α-Synuclein Fibrils and Enhance their Pathogenicity in a TREM2-Dependent Manner.
小胶质细胞以 TREM2 依赖的方式处理 α-突触核蛋白原纤维并增强其致病性
Autophagosomes anchor an AKAP11-dependent regulatory checkpoint that shapes neuronal PKA signaling
自噬体锚定一个依赖于 AKAP11 的调控检查点,该检查点塑造神经元 PKA 信号传导。
Inhibition of CD36 ameliorates mouse spinal cord injury by accelerating microglial lipophagy.
抑制 CD36 可通过加速小胶质细胞脂质自噬来改善小鼠脊髓损伤
The cholesterol 24-hydroxylase CYP46A1 promotes α-synuclein pathology in Parkinson's disease
胆固醇24-羟化酶CYP46A1促进帕金森病中的α-突触核蛋白病理
Mesenchymal stem cells overexpressing neuropeptide S promote the recovery of rats with spinal cord injury by activating the PI3K/AKT/GSK3β signaling pathway.
间充质干细胞过度表达神经肽S,通过激活PI3K/AKT/GSK3β信号通路促进脊髓损伤大鼠的恢复
Novel strategy to target glioblastoma-initiating cells using a braintropic adeno-associated virus carrying a miR-dependent genome-editing system.
利用携带 miR 依赖性基因组编辑系统的嗜脑腺相关病毒靶向胶质母细胞瘤起始细胞的新策略
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