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Dpp9-P2A-EGFP-T2A-CreERT2
製品ID :
I001087
系統:
C57BL/6JCya
状況:
説明:
The TGA stop codon of the mouse Dpp9 gene is replaced by P2A-EGFP-T2A-CreERT2. When this strain is crossed with mice containing loxP sites, after tamoxifen induction in the offspring mice, sequence recombination between loxP sites mediated by Cre recombinase will be triggered. In addition, an enhanced green fluorescent protein (EGFP) expression element is inserted before the CreERT2 recombinase element in this model, which can also be used for the tracking of Dpp9-positive cells.
The TGA stop codon of the mouse Dpp9 gene is replaced by P2A-EGFP-T2A-CreERT2. When this strain is crossed with mice containing loxP sites, after tamoxifen induction in the offspring mice, sequence recombination between loxP sites mediated by Cre recombinase will be triggered. In addition, an enhanced green fluorescent protein (EGFP) expression element is inserted before the CreERT2 recombinase element in this model, which can also be used for the tracking of Dpp9-positive cells.
Dpp9-KO
製品ID :
S-KO-05847
系統:
C57BL/6JCya
状況:
説明:
Dpp9 is located on chromosome 17 of mice. Nuclease Technology will be used to design sgRNA; Dpp9 knockout mice will be obtained by applying high-throughput electroporation of fertilized eggs. After sexual maturity, sperm were collected for cryopreservation.
Dpp9 is located on chromosome 17 of mice. Nuclease Technology will be used to design sgRNA; Dpp9 knockout mice will be obtained by applying high-throughput electroporation of fertilized eggs. After sexual maturity, sperm were collected for cryopreservation.
Dpp9-flox
製品ID :
S-CKO-06793
系統:
C57BL/6JCya
状況:
説明:
Dpp9 is located on chromosome 17 of mice. SgRNA and ssDNA were designed using Nuclease Technology; Dpp9 conditional knockout mice were obtained by high-throughput electroporation of fertilized eggs. After sexual maturity, sperm were collected for cryopreservation.
Dpp9 is located on chromosome 17 of mice. SgRNA and ssDNA were designed using Nuclease Technology; Dpp9 conditional knockout mice were obtained by high-throughput electroporation of fertilized eggs. After sexual maturity, sperm were collected for cryopreservation.
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