这是一篇来自已证抗体库的有关
小鼠 Epha4的综述,是根据13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Epha4 抗体。
Epha4 同义词: 2900005C20Rik; AI385584; Cek8; Hek8; Sek; Sek1; Tyro1; ephrin type-A receptor 4; tyrosine-protein kinase receptor MPK-3; tyrosine-protein kinase receptor SEK-1
赛默飞世尔
小鼠 单克隆(4C8H5) | | 赛默飞世尔 Epha4抗体(Invitrogen, 37-1600)被用于被用于免疫印迹在小鼠样品上浓度为1:1000 (图 3a). Development (2017) ncbi |
小鼠 单克隆(4C8H5) | - 免疫沉淀; 人类; 图 4a
- 免疫印迹; 人类; 图 4a
| 赛默飞世尔 Epha4抗体(生活技术, 37-1600)被用于被用于免疫沉淀在人类样品上 (图 4a) 和 被用于免疫印迹在人类样品上 (图 4a). Exp Cell Res (2016) ncbi |
小鼠 单克隆(4C8H5) | | 赛默飞世尔 Epha4抗体(Invitrogen, 37-1600)被用于被用于免疫印迹在小鼠样品上浓度为1:200. Eur J Neurosci (2014) ncbi |
小鼠 单克隆(4C8H5) | | 赛默飞世尔 Epha4抗体(Invitrogen, 37-1600)被用于被用于免疫印迹在小鼠样品上浓度为1:200 (图 3). Eur J Neurosci (2013) ncbi |
小鼠 单克隆(4C8H5) | | 赛默飞世尔 Epha4抗体(Zymed, 37-1600)被用于被用于免疫印迹在小鼠样品上浓度为1:1000 (图 s2). Hum Mol Genet (2013) ncbi |
小鼠 单克隆(4C8H5) | | 赛默飞世尔 Epha4抗体(Invitrogen, 37-1600)被用于被用于免疫组化在小鼠样品上. Mol Cell Biol (2013) ncbi |
小鼠 单克隆(4C8H5) | | 赛默飞世尔 Epha4抗体(Zymed, 37-1600)被用于被用于免疫印迹在小鼠样品上浓度为1:1000 (图 4). Nat Med (2012) ncbi |
小鼠 单克隆(4C8H5) | | 赛默飞世尔 Epha4抗体(Zymed, 4C8H5)被用于被用于免疫沉淀在小鼠样品上 (图 5). PLoS ONE (2008) ncbi |
小鼠 单克隆(4C8H5) | | 赛默飞世尔 Epha4抗体(Zymed, 4C8H5)被用于被用于免疫印迹在小鼠样品上 (图 1). Neuron (2007) ncbi |
艾博抗(上海)贸易有限公司
兔 多克隆 | - immunohistochemistry - free floating section; 小鼠; 1:100; 图 3
| 艾博抗(上海)贸易有限公司 Epha4抗体(Abcam, ab5396)被用于被用于immunohistochemistry - free floating section在小鼠样品上浓度为1:100 (图 3). Mol Med Rep (2017) ncbi |
圣克鲁斯生物技术
小鼠 单克隆(35) | | 圣克鲁斯生物技术 Epha4抗体(Santa Cruz Biotechnology, sc-135897)被用于被用于免疫印迹在大鼠样品上. PLoS ONE (2014) ncbi |
安迪生物R&D
山羊 多克隆 | | 安迪生物R&D Epha4抗体(R&D Systems, AF641)被用于被用于免疫组化-冰冻切片在小鼠样品上浓度为1:150. J Comp Neurol (2012) ncbi |
碧迪BD
小鼠 单克隆(35/EphA4) | | 碧迪BD Epha4抗体(BD Biosciences, 610471)被用于被用于免疫组化-石蜡切片在小鼠样品上浓度为1:100. Development (2013) ncbi |
Rothe M, Kanwal N, Dietmann P, Seigfried F, Hempel A, Schütz D,
et al. An Epha4/Sipa1l3/Wnt pathway regulates eye development and lens maturation. Development. 2017;144:321-333
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Feng L, Shu Y, Wu Q, Liu T, Long H, Yang H,
et al. EphA4 may contribute to microvessel remodeling in the hippocampal CA1 and CA3 areas in a mouse model of temporal lobe epilepsy. Mol Med Rep. 2017;15:37-46
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Jurek A, Genander M, Kundu P, Catchpole T, He X, Strååt K,
et al. Eph receptor interclass cooperation is required for the regulation of cell proliferation. Exp Cell Res. 2016;348:10-22
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Joly S, Jordi N, Schwab M, Pernet V. The Ephrin receptor EphA4 restricts axonal sprouting and enhances branching in the injured mouse optic nerve. Eur J Neurosci. 2014;40:3021-31
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Vargas L, Leal N, Estrada L, Gonz lez A, Serrano F, Araya K,
et al. EphA4 activation of c-Abl mediates synaptic loss and LTP blockade caused by amyloid-? oligomers. PLoS ONE. 2014;9:e92309
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Kempf A, Montani L, Petrinovic M, Schroeter A, Weinmann O, Patrignani A,
et al. Upregulation of axon guidance molecules in the adult central nervous system of Nogo-A knockout mice restricts neuronal growth and regeneration. Eur J Neurosci. 2013;38:3567-79
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Yang Z, Zimmerman S, BRAKEMAN P, Beaudoin G, Reichardt L, MARCIANO D. De novo lumen formation and elongation in the developing nephron: a central role for afadin in apical polarity. Development. 2013;140:1774-84
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Lemmens R, Jaspers T, Robberecht W, Thijs V. Modifying expression of EphA4 and its downstream targets improves functional recovery after stroke. Hum Mol Genet. 2013;22:2214-20
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Semerdjieva S, Abdul Razak H, Salim S, Yáñez Muñoz R, Chen P, Tarabykin V,
et al. Activation of EphA receptors mediates the recruitment of the adaptor protein Slap, contributing to the downregulation of N-methyl-D-aspartate receptors. Mol Cell Biol. 2013;33:1442-55
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Van Hoecke A, Schoonaert L, Lemmens R, Timmers M, Staats K, Laird A,
et al. EPHA4 is a disease modifier of amyotrophic lateral sclerosis in animal models and in humans. Nat Med. 2012;18:1418-22
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Hashimoto M, Ito R, Kitamura N, Namba K, Hisano Y. Epha4 controls the midline crossing and contralateral axonal projections of inferior olive neurons. J Comp Neurol. 2012;520:1702-20
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Yumoto N, Wakatsuki S, Kurisaki T, Hara Y, Osumi N, Frisen J,
et al. Meltrin beta/ADAM19 interacting with EphA4 in developing neural cells participates in formation of the neuromuscular junction. PLoS ONE. 2008;3:e3322
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Beg A, Sommer J, Martin J, Scheiffele P. alpha2-Chimaerin is an essential EphA4 effector in the assembly of neuronal locomotor circuits. Neuron. 2007;55:768-78
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