The targeting vector consisting of fragments of 2.9 kb, 3.8 kb and 3.3 kb in size containing the distal promoter sequence, the sequence upstream of exon 1, and the sequence downstream of exon 1, respectively, were used to insert a CreER(T2)-IRES-EGFP cassette and an FRT-flanked neomycin cassette in the 5 end of the 3.3-kb fragment. The linearized construct was electroporated into C57BL/6J mouse ES cells. The neomycin cassette was removed by breeding with C57BL/6J mice expressing Flp-recombinase. With CreER inserted into exon 1, Cxcr4CreER does not produce functional Cxcr4 and homozygous mice bearing this allele are fully deficient in Cxcr4, as verified by immunohistochemistry. (J:288822)
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模型ID
品系来源
等位基因类型
突变
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C57BL/6J
Targeted
Insertion
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1
1
8

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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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