The cells are fibroblasts prepared from embryos of the Engase -knockout mice (congenic (>96%) to C57BL/6J mice). They were immortalized by transfection with a plasmid encoding the SV40 large T antigen.
細胞特性(寄託者記述:日)
当該細胞は、 Engaseノックアウトマウスの胎児から調製した線維芽細胞であり(C57BL/6J バックグラウンド(>96%))、 SV40 由来 large T 抗原で不死化したものである。
使用条件(英)
A prior written permission of the approver(Depositor) is necessary for any kind of use including academic use and for-profit use.
Regarding MTA between user institutions and RIKEN BRC, there are two kinds of MTA, not-for-profit academic purpose (C-XXXX) and for-profit research purpose (C-XXXXp) , depending on the sort of user institutions and the purposes of use. Please use an appropriate MTA(to see). In relation to commercial use and use for patent filing, first of all Please contact RIKEN BRC (cellbank.brc@riken.jp).
23553
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530(4):719-724
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PubMed ID: 31875565
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Fujihira H, Masahara-Negishi Y, Tamura M, Huang C, Harada Y, Wakana S, Takakura D, Kawasaki N, Taniguchi N, Kondoh G, Yamashita T, Funakoshi Y, Suzuki T.
Lethality of mice bearing a knockout of the Ngly1-gene is partially rescued by the additional deletion of the Engase genePLoS Genet
2017
13(4):e1006696
PubMed ID: 28426790
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Harada Y, Huang C, Yamaki S, Dohmae N, Suzuki T.
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2016
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PubMed ID: 26858256
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Endo-β-N-acetylglucosaminidase forms N-GlcNAc protein aggregates during ER-associated degradation in Ngly1-defective cellsProc Natl Acad Sci U S A
2015
112(5):1398-403
PubMed ID: 25605922
DOI: 10.1073/pnas.1414593112