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5 件の結果が “18187” で取得されました
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Nrp2-tdTomato-IRES-CreERT2
製品ID :
I001091
系統:
C57BL/6JCya
状況:
説明:
The coding sequence of exon 1 to a partial sequence of intron 1 of the mouse Nrp2 gene is replaced by Kozak-tdTomato-IRES-CreERT2-WPRE-BGH pA. When this strain is crossed with mice containing loxP sites, after tamoxifen induction in the offspring, it is expected to trigger Cre-recombinase-mediated sequence recombination between loxP sites in yolk sac, venous and lymphatic endothelial cells, as well as in peripheral sensory ganglia, and primitive blood cells generated in lung buds. In addition, a tdTomato red fluorescent expression element is inserted before the CreERT2 recombinase element in this model, allowing for the tracking of Nrp2-positive cells.
The coding sequence of exon 1 to a partial sequence of intron 1 of the mouse Nrp2 gene is replaced by Kozak-tdTomato-IRES-CreERT2-WPRE-BGH pA. When this strain is crossed with mice containing loxP sites, after tamoxifen induction in the offspring, it is expected to trigger Cre-recombinase-mediated sequence recombination between loxP sites in yolk sac, venous and lymphatic endothelial cells, as well as in peripheral sensory ganglia, and primitive blood cells generated in lung buds. In addition, a tdTomato red fluorescent expression element is inserted before the CreERT2 recombinase element in this model, allowing for the tracking of Nrp2-positive cells.
Fundc1-KO
製品ID :
S-KO-18187
系統:
C57BL/6JCya
状況:
説明:
Fundc1 is located on chromosome X of mice. Nuclease Technology was used to design sgRNA; Fundc1 knockout mice were obtained by applying high-throughput electroporation of fertilized eggs. After sexual maturity, sperm were collected for cryopreservation.
Fundc1 is located on chromosome X of mice. Nuclease Technology was used to design sgRNA; Fundc1 knockout mice were obtained by applying high-throughput electroporation of fertilized eggs. After sexual maturity, sperm were collected for cryopreservation.
Lcp1-flox
製品ID :
S-CKO-18187
系統:
C57BL/6JCya
状況:
説明:
Lcp1 is located on chromosome 14 of mice. SgRNA and ssDNA were designed using Nuclease Technology; Lcp1 conditional knockout mice were obtained by high-throughput electroporation of fertilized eggs. After sexual maturity, sperm were collected for cryopreservation.
Lcp1 is located on chromosome 14 of mice. SgRNA and ssDNA were designed using Nuclease Technology; Lcp1 conditional knockout mice were obtained by high-throughput electroporation of fertilized eggs. After sexual maturity, sperm were collected for cryopreservation.
Nrp2-KO
製品ID :
S-KO-23763
系統:
C57BL/6JCya
状況:
説明:
Nrp2 is located on chromosome 1 of mice. Nuclease Technology was used to design sgRNA; Nrp2 knockout mice were obtained by applying high-throughput electroporation of fertilized eggs. After sexual maturity, sperm were collected for cryopreservation.
Nrp2 is located on chromosome 1 of mice. Nuclease Technology was used to design sgRNA; Nrp2 knockout mice were obtained by applying high-throughput electroporation of fertilized eggs. After sexual maturity, sperm were collected for cryopreservation.
Nrp2-flox
製品ID :
S-CKO-17549
系統:
C57BL/6JCya
状況:
説明:
Nrp2 is located on chromosome 1 of mice. SgRNA and ssDNA were designed using Nuclease Technology; Nrp2 conditional knockout mice were obtained by high-throughput electroporation of fertilized eggs. After sexual maturity, sperm were collected for cryopreservation.
Nrp2 is located on chromosome 1 of mice. SgRNA and ssDNA were designed using Nuclease Technology; Nrp2 conditional knockout mice were obtained by high-throughput electroporation of fertilized eggs. After sexual maturity, sperm were collected for cryopreservation.
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