这是一篇来自已证抗体库的有关
大鼠 Shank3的综述,是根据6篇发表使用所有方法的文章归纳的。这综述旨在帮助来邦网的访客找到最适合Shank3 抗体。
Shank3 同义词: Prosap2; SH3 and multiple ankyrin repeat domains protein 3; SH3/ankyrin domain gene 3; SPANK-2; Shank postsynaptic density protein 3a; proline-rich synapse-associated protein 2
Synaptic Systems
兔 多克隆(/) | | Synaptic Systems Shank3抗体(SYSY, 162302)被用于被用于免疫印迹在大鼠样品上 (图 3). Front Cell Neurosci (2015) ncbi |
Neuromab
小鼠 单克隆(N69/46) | - 免疫印迹基因敲除验证; 大鼠; 1:100; 图 s1b
| Neuromab Shank3抗体(NeuroMab, N69/46)被用于被用于免疫印迹基因敲除验证在大鼠样品上浓度为1:100 (图 s1b). elife (2017) ncbi |
小鼠 单克隆(N367/62) | | Neuromab Shank3抗体(NeuroMab, N367/62)被用于被用于免疫印迹在大鼠样品上浓度为1:100 (图 1b). elife (2017) ncbi |
小鼠 单克隆(N367/62) | | Neuromab Shank3抗体(NeuroMab, 75-344)被用于被用于免疫印迹在小鼠样品上 (图 7). Nat Commun (2016) ncbi |
小鼠 单克隆(N69/46) | | Neuromab Shank3抗体(Neuromab, 75-109)被用于被用于免疫印迹在大鼠样品上浓度为1:10. Neuroscience (2015) ncbi |
小鼠 单克隆(N69/46) | | Neuromab Shank3抗体(UC Davis/NIH NeuroMab Facility, 75-109)被用于被用于免疫沉淀在小鼠样品上 (图 1). Int J Mol Sci (2015) ncbi |
小鼠 单克隆(N69/46) | | Neuromab Shank3抗体(Neuromab, 75-109)被用于被用于免疫组化在小鼠样品上. Hear Res (2015) ncbi |
Harony Nicolas H, Kay M, Hoffmann J, Klein M, Bozdagi Gunal O, Riad M,
et al. Oxytocin improves behavioral and electrophysiological deficits in a novel Shank3-deficient rat. elife. 2017;6:
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Frank R, Komiyama N, Ryan T, Zhu F, O Dell T, Grant S. NMDA receptors are selectively partitioned into complexes and supercomplexes during synapse maturation. Nat Commun. 2016;7:11264
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Garcia Manteiga J, Bonfiglio S, Folladori L, Malosio M, Lazarevic D, Stupka E,
et al. REST-Governed Gene Expression Profiling in a Neuronal Cell Model Reveals Novel Direct and Indirect Processes of Repression and Up-Regulation. Front Cell Neurosci. 2015;9:438
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Farley M, Swulius M, Waxham M. Electron tomographic structure and protein composition of isolated rat cerebellar, hippocampal and cortical postsynaptic densities. Neuroscience. 2015;304:286-301
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Benthani F, Tran P, Currey N, Ng I, Giry Laterriere M, Carey L,
et al. Proteogenomic Analysis Identifies a Novel Human SHANK3 Isoform. Int J Mol Sci. 2015;16:11522-30
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Braude J, Vijayakumar S, Baumgarner K, Laurine R, Jones T, Jones S,
et al. Deletion of Shank1 has minimal effects on the molecular composition and function of glutamatergic afferent postsynapses in the mouse inner ear. Hear Res. 2015;321:52-64
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