Recombineering of the BAC clone RP24-386G1 containing the Foxa2 locus generated a targeting vector designed to replace the stop codon of Foxa2 and introduce sequences encoding the ERAV 2A peptide, a human histone H2B/EGFP fusion protein (protein is expressed in the cell nucleus), the Thosea asigna virus 2A peptide and cre/ERT2 fusion protein. A self-excising ACN cassette (containing the neo resistance marker) was also included. The vector was electroporated into ES cells for homologous recombination. Correctly targeted clones were used to produce chimeras. Chimeras were bred to C57BL/6J females, with the ACN cassette self-excising during passage through the germline. Two independent ES cell clones (3 and 22) produced mouse lines which had the same phenotpe, and the line derived from #22 was analyzed further. (J:194054)
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基础信息

模型ID
品系来源
等位基因类型
突变
遗传方式
相关基因
相关疾病
参考文献
(C57BL/6NCrlj x CBA/JNCrlj)F1
Targeted
Insertion, Intragenic deletion
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1
1
8

表型特征

标签摘要:
hm: 纯合子
ht: 杂合子
cn: 条件基因型
cx: 复合型:涉及多基因组
tg: 转基因
ot: 其他:半合子、不确定...
(F): 雌性
(M): 雄性
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N: 正常表型
(#): 上标括号内为相关疾病数量
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