The transgene was established using a mouse genomic BAC clone RP23-55P20, which encodes cadherin-related family member (Cdhr)1 gene by inserting a loxP-LacZ-loxP-tTA cassette at 25 bp upstream of the translation initiation site of this gene. In this cassette, the LacZ gene followed by a transcription termination site was flanked by loxP sequences and used as a STOP sequence, which followed by the tetracycline-controlled transactivator (tTA) gene in an optimized form for mammalian expression. The original loxP site in the vector backbone was subsequently deleted using p23loxZeo. Among the six independent transgenic lines obtained, one unnumbered line was characterized by the OB-specific strongest expression of the internal LacZ gene. (J:288786)
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基础信息

模型ID
品系来源
等位基因类型
突变
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C57BL/6
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Insertion
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1

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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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