这是一篇来自已证抗体库的有关
人类 XPG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XPG 抗体。
XPG 同义词: COFS3; ERCC5-201; ERCM2; UVDR; XPG; XPGC; DNA repair protein complementing XP-G cells; DNA excision repair protein ERCC-5; XPG-complementing protein; excision repair cross-complementation group 5; excision repair cross-complementing rodent repair deficiency, complementation group 5; xeroderma pigmentosum, complementation group G
Bethyl
兔 多克隆 | | Bethyl XPG抗体(Bethyl, A301-484A)被用于被用于免疫细胞化学在人类样品上 (图 4e). Nucleic Acids Res (2018) ncbi |
兔 多克隆 | | Bethyl XPG抗体(Bethyl, A301-484A)被用于被用于免疫印迹在人类样品上 (图 3). Mol Cell Biol (2015) ncbi |
兔 多克隆 | | Bethyl XPG抗体(Bethyl Laboratories, A301-484A)被用于被用于免疫印迹在人类样品上浓度为1:3000 (图 1). Cell Cycle (2015) ncbi |
圣克鲁斯生物技术
小鼠 单克隆(8H7) | | 圣克鲁斯生物技术 XPG抗体(Santa Cruz Biotechnology, sc-13563)被用于被用于免疫细胞化学在人类样品上浓度为1:25. Genes Cells (2015) ncbi |
赛默飞世尔
小鼠 单克隆(8H7) | | 赛默飞世尔 XPG抗体(Thermo Scientific, 8H7)被用于被用于免疫细胞化学在小鼠样品上浓度为1:400 (图 2b). Nat Commun (2015) ncbi |
武汉三鹰
兔 多克隆 | | 武汉三鹰 XPG抗体(ProteinTech, 11331-1-AP)被用于被用于其他在人类样品上 (图 4c). Cancer Cell (2018) ncbi |
Sabatella M, Theil A, Ribeiro Silva C, Slyskova J, Thijssen K, Voskamp C,
et al. Repair protein persistence at DNA lesions characterizes XPF defect with Cockayne syndrome features. Nucleic Acids Res. 2018;46:9563-9577
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Ng P, Li J, Jeong K, Shao S, Chen H, Tsang Y,
et al. Systematic Functional Annotation of Somatic Mutations in Cancer. Cancer Cell. 2018;33:450-462.e10
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van Cuijk L, van Belle G, Turkyilmaz Y, Poulsen S, Janssens R, Theil A,
et al. SUMO and ubiquitin-dependent XPC exchange drives nucleotide excision repair. Nat Commun. 2015;6:7499
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Narita T, Narita K, Takedachi A, Saijo M, Tanaka K. Regulation of Transcription Elongation by the XPG-TFIIH Complex Is Implicated in Cockayne Syndrome. Mol Cell Biol. 2015;35:3178-88
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Han C, Wani G, Zhao R, Qian J, Sharma N, He J,
et al. Cdt2-mediated XPG degradation promotes gap-filling DNA synthesis in nucleotide excision repair. Cell Cycle. 2015;14:1103-15
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Kikuchi Y, Umemura H, Nishitani S, Iida S, Fukasawa R, Hayashi H,
et al. Human mediator MED17 subunit plays essential roles in gene regulation by associating with the transcription and DNA repair machineries. Genes Cells. 2015;20:191-202
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