myc ddk flag (OriGene)
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myc ddk flag
Myc Ddk Flag, supplied by OriGene, used in various techniques. Bioz Stars score: 94/100, based on 2 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/myc+ddk+flag/NCF2+(NM_000433)+Human+Tagged+ORF+Clone/pmc12936047-49-19-24
Average 94 stars, based on 2 article reviews
Myc Ddk Flag, supplied by OriGene, used in various techniques. Bioz Stars score: 94/100, based on 2 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/myc+ddk+flag/NCF2+(NM_000433)+Human+Tagged+ORF+Clone/pmc12936047-49-19-24
Average 94 stars, based on 2 article reviews
myc ddk flag - by Bioz Stars,
2026-09
94/100 stars
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Expressing:Article Title: Golgi-localized Ring Finger Protein 121 is necessary for MYCN-driven neuroblastoma tumorigenesis Article Snippet: Cell density was adjusted so that for all assays, 80–90% confluency would be achieved by the endpoint of the assay in the control condition. siRNA’s used were siRNF121-1: GAAAUGGUCCUCAUCCUCA (Dharmacon: J-007011-06) and siRNF121-4: CCAUAGGGUUCUACAGCGA (Dharmacon: J-007011-08) or non-targeting control siRNAs (ONTARGETplus siRNA, #D-001810-0X, Dharmacon). .. Expression plasmids of pCMV6-Empty Vector and pCMV6-hRNF121 wild type (WT) with Article Title: NCF2 facilitates M2 macrophage polarization in glioblastoma through activation of the notch1–osteopontin axis Article Snippet: .. A mammalian expression plasmid encoding the full-length open reading frame (ORF) of human NCF2 ( NM_000433 ) tagged with Article Title: Mutational and functional analysis of Glucose transporter I deficiency syndrome. Article Snippet: Molecular Genetics and Metabolism xxx (2015) xxx–xxx YMGME-05940; No. of pages: 6; 4C: 3, 4, 5 Contents lists available at ScienceDirect Molecular Genetics and Metabolism j ourna l homepage: www.e lsev ie r .com/ locate /ymgme Mutational and functional analysis of Glucose transporter I deficiency syndrome Sachie Nakamura a, Hitoshi Osaka a,⁎, Shinichi Muramatsu b,c, Shiho Aoki a, Eriko F. Jimbo a, Takanori Yamagata a a Department of Pediatrics, Jichi Medical University, Tochigi, Japan b Division of Neurology, Jichi Medical University, Tochigi, Japan c Center for Gene and Cell Therapy, The Institute of Medical Science, The University of Tokyo, Japan ⁎ Corresponding author at: Dept. of Pediatrics, Jichi Me Shimotsuke-shi, Tochigi 329-0498, Japan.. E-mail address: hosaka@jichi.ac.jp (H. Osaka). http://dx.doi.org/10.1016/j.ymgme.2015.08.006 1096-7192/© 2015 Elsevier Inc. All rights reserved.. Please cite this article as: S. Nakamura, et al., (2015), http://dx.doi.org/10.1016/j.ymgme.2 a b s t r a c t a r t i c l e i n f o Article history: Received 8 July 2015 Received in revised form 9 August 2015 Accepted 9 August 2015 Available online xxxx Keywords: Glucose transporter I deficiency syndrome (GLUT1-DS) GLUT1 SLC2A1 Functional assay 2-deoxyglucose uptake Objective: We investigated a correlation between a mutation in the SLC2A1 gene and functional disorders in Glucose transporter I deficiency syndrome (GLUT1DS). Mutagenesis:Article Title: Golgi-localized Ring Finger Protein 121 is necessary for MYCN-driven neuroblastoma tumorigenesis Article Snippet: Cell density was adjusted so that for all assays, 80–90% confluency would be achieved by the endpoint of the assay in the control condition. siRNA’s used were siRNF121-1: GAAAUGGUCCUCAUCCUCA (Dharmacon: J-007011-06) and siRNF121-4: CCAUAGGGUUCUACAGCGA (Dharmacon: J-007011-08) or non-targeting control siRNAs (ONTARGETplus siRNA, #D-001810-0X, Dharmacon). .. Expression plasmids of pCMV6-Empty Vector and pCMV6-hRNF121 wild type (WT) with Sequencing:Article Title: Golgi-localized Ring Finger Protein 121 is necessary for MYCN-driven neuroblastoma tumorigenesis Article Snippet: Cell density was adjusted so that for all assays, 80–90% confluency would be achieved by the endpoint of the assay in the control condition. siRNA’s used were siRNF121-1: GAAAUGGUCCUCAUCCUCA (Dharmacon: J-007011-06) and siRNF121-4: CCAUAGGGUUCUACAGCGA (Dharmacon: J-007011-08) or non-targeting control siRNAs (ONTARGETplus siRNA, #D-001810-0X, Dharmacon). .. Expression plasmids of pCMV6-Empty Vector and pCMV6-hRNF121 wild type (WT) with Plasmid Preparation:Article Title: NCF2 facilitates M2 macrophage polarization in glioblastoma through activation of the notch1–osteopontin axis Article Snippet: .. A mammalian expression plasmid encoding the full-length open reading frame (ORF) of human NCF2 ( NM_000433 ) tagged with Article Title: Mutational and functional analysis of Glucose transporter I deficiency syndrome. Article Snippet: Molecular Genetics and Metabolism xxx (2015) xxx–xxx YMGME-05940; No. of pages: 6; 4C: 3, 4, 5 Contents lists available at ScienceDirect Molecular Genetics and Metabolism j ourna l homepage: www.e lsev ie r .com/ locate /ymgme Mutational and functional analysis of Glucose transporter I deficiency syndrome Sachie Nakamura a, Hitoshi Osaka a,⁎, Shinichi Muramatsu b,c, Shiho Aoki a, Eriko F. Jimbo a, Takanori Yamagata a a Department of Pediatrics, Jichi Medical University, Tochigi, Japan b Division of Neurology, Jichi Medical University, Tochigi, Japan c Center for Gene and Cell Therapy, The Institute of Medical Science, The University of Tokyo, Japan ⁎ Corresponding author at: Dept. of Pediatrics, Jichi Me Shimotsuke-shi, Tochigi 329-0498, Japan.. E-mail address: hosaka@jichi.ac.jp (H. Osaka). http://dx.doi.org/10.1016/j.ymgme.2015.08.006 1096-7192/© 2015 Elsevier Inc. All rights reserved.. Please cite this article as: S. Nakamura, et al., (2015), http://dx.doi.org/10.1016/j.ymgme.2 a b s t r a c t a r t i c l e i n f o Article history: Received 8 July 2015 Received in revised form 9 August 2015 Accepted 9 August 2015 Available online xxxx Keywords: Glucose transporter I deficiency syndrome (GLUT1-DS) GLUT1 SLC2A1 Functional assay 2-deoxyglucose uptake Objective: We investigated a correlation between a mutation in the SLC2A1 gene and functional disorders in Glucose transporter I deficiency syndrome (GLUT1DS). |
