Anti-MAP2 antibody [HM-2] - Neuronal Marker (Ab11267)
Mtap2, Map2, Microtubule-associated protein 2, MAP-2
用户验证的应用
推荐稀释比例
- WB1-2 µg/mL
- ICC2 µg/mL Fix cells in 4% paraformaldehyde/PBS for 45 min; then permeabilise cells with 0.2% Triton X-100 in PBS for 5 min (see Farah et al) OR fix in 4% paraformaldehyde (containing 0.2% picric acid in 0.1 M phosphate buffer, pH 6.9) for 15 min at room temperature (see O' Hare et al).
详细信息
背景信息
What is this antibody validated in? Anti-MAP2 antibody [HM-2] (ab11267) is a mouse monoclonal antibody and is validated for use in Western Blot (WB) in Rat samples. What is the molecular weight of MAP2? Anti-MAP2 [HM-2] (ab11267) specifically detects a band for MAP2 (UniProt: P11137) at a molecular weight of 200kDa. Trusted by the scientific community Anti-MAP2 [HM-2] (ab11267) was first used in a scientific publication in 2004 and has been cited over 170 times in peer-reviewed journals. Reviewed by scientists Anti-MAP2 [HM-2] (ab11267) has over 5 independent reviews from customers.
文献引用 (176)
Temporal regulation of human reactive astrocytes reveals their capacity for antigen presentation.
人类反应性星形胶质细胞的时间调控揭示了它们呈递抗原的能力。
Ubiquitin ligase Nedd4 regulates the abundance and toxicity of mutant huntingtin.
泛素连接酶 Nedd4 调节突变亨廷顿蛋白的丰度和毒性。
KCNB1 mutation impairs neuronal differentiation by disrupting gene expression temporal regulation and neuron-specific pathways.
KCNB1 突变会破坏基因表达的时间调控和神经元特异性通路，从而损害神经元分化。
Gastrodin alleviates neuronal damage in epileptic cell models by targeting P2RY12 to inhibit microglial hyperactivation.
天麻素通过靶向 P2RY12 抑制小胶质细胞过度激活，从而减轻癫痫细胞模型中的神经元损伤。
Genetically Programmed Single-Component Protein Hydrogel for Spinal Cord Injury Repair.
用于脊髓损伤修复的基因编程单组分蛋白水凝胶
p-Coumaric acid alleviates neuronal damage in ischemic stroke mice by promoting BACH1 nuclear export and degradation.
对香豆酸通过促进 BACH1 核输出和降解来减轻缺血性中风小鼠的神经元损伤
In utero rescue of neurological dysfunction in a mouse model of Wiedemann-Steiner syndrome
在维德曼-施泰纳综合征小鼠模型中，通过子宫内干预挽救神经功能障碍
Reduced mesencephalic astrocyte-derived neurotrophic factor expression by mutant androgen receptor contributes to neurodegeneration in a model of spinal and bulbar muscular atrophy pathology
突变雄激素受体导致中脑星形胶质细胞衍生神经营养因子表达减少，从而促进脊髓延髓肌萎缩症病理模型中的神经退行性变。
Prion replication in organotypic brain slice cultures is distinct from in vivo inoculation and is species dependent.
朊病毒在器官型脑片培养物中的复制与体内接种不同，并且具有物种依赖性
Cathepsin B deficiency disrupts cortical development via PEG3, leading to depression-like behavior.
组织蛋白酶 B 缺乏通过 PEG3 破坏皮层发育，导致类似抑郁的行为
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