フィルター
6 件の結果が “16333” で取得されました
並べ替える:
アルファベット順（A-Z）
ベストセラー
Ins1-CreERT2
製品ID :
I001151
系統:
C57BL/6JCya
状況:
説明:
The partial coding region of exon 2 of the mouse Ins1 gene was replaced with the "Kozak- CreERT2-WPRE-BGH pA" cassette. CreERT2 recombinase is expressed under the regulatory control of Ins1 gene elements. This model is a Tamoxifen-inducible Cre mouse, and when crossed with mice containing loxP sites, the offspring mice are expected to undergo sequence recombination between loxP sites mediated by Cre recombinase in the pancreas following Tamoxifen induction.
The partial coding region of exon 2 of the mouse Ins1 gene was replaced with the "Kozak- CreERT2-WPRE-BGH pA" cassette. CreERT2 recombinase is expressed under the regulatory control of Ins1 gene elements. This model is a Tamoxifen-inducible Cre mouse, and when crossed with mice containing loxP sites, the offspring mice are expected to undergo sequence recombination between loxP sites mediated by Cre recombinase in the pancreas following Tamoxifen induction.
Sypl1-KO
製品ID :
S-KO-16333
系統:
C57BL/6JCya
状況:
説明:
Sypl1 is located on chromosome 12 of mice. Nuclease Technology will be used to design sgRNA; Sypl1 knockout mice will be obtained by applying high-throughput electroporation of fertilized eggs. After sexual maturity, sperm were collected for cryopreservation.
Sypl1 is located on chromosome 12 of mice. Nuclease Technology will be used to design sgRNA; Sypl1 knockout mice will be obtained by applying high-throughput electroporation of fertilized eggs. After sexual maturity, sperm were collected for cryopreservation.
Ins1-KO
製品ID :
S-KO-02671
系統:
C57BL/6JCya
状況:
説明:
Ins1 is located on chromosome 19 of mice. Nuclease Technology was used to design sgRNA; Ins1 knockout mice were obtained by applying high-throughput electroporation of fertilized eggs. After sexual maturity, sperm were collected for cryopreservation.
Ins1 is located on chromosome 19 of mice. Nuclease Technology was used to design sgRNA; Ins1 knockout mice were obtained by applying high-throughput electroporation of fertilized eggs. After sexual maturity, sperm were collected for cryopreservation.
Ins1-KO
製品ID :
S-KO-20870
系統:
C57BL/6JCya
状況:
説明:
Ins1 is located on chromosome 19 of mice. Nuclease Technology will be used to design sgRNA; Ins1 knockout mice will be obtained by applying high-throughput electroporation of fertilized eggs. After sexual maturity, sperm were collected for cryopreservation.
Ins1 is located on chromosome 19 of mice. Nuclease Technology will be used to design sgRNA; Ins1 knockout mice will be obtained by applying high-throughput electroporation of fertilized eggs. After sexual maturity, sperm were collected for cryopreservation.
Ins1-flox
製品ID :
S-CKO-18427
系統:
C57BL/6JCya
状況:
説明:
Ins1 is located on chromosome 19 of mice. SgRNA and ssDNA will be designed using Nuclease Technology; Ins1 conditional knockout mice will be obtained by high-throughput electroporation of fertilized eggs. After sexual maturity, sperm will be collected for cryopreservation.
Ins1 is located on chromosome 19 of mice. SgRNA and ssDNA will be designed using Nuclease Technology; Ins1 conditional knockout mice will be obtained by high-throughput electroporation of fertilized eggs. After sexual maturity, sperm will be collected for cryopreservation.
Pnpla5-flox
製品ID :
S-CKO-16333
系統:
C57BL/6JCya
状況:
説明:
Pnpla5 is located on chromosome 15 of mice. SgRNA and ssDNA will be designed using Nuclease Technology; Pnpla5 conditional knockout mice will be obtained by high-throughput electroporation of fertilized eggs. After sexual maturity, sperm will be collected for cryopreservation.
Pnpla5 is located on chromosome 15 of mice. SgRNA and ssDNA will be designed using Nuclease Technology; Pnpla5 conditional knockout mice will be obtained by high-throughput electroporation of fertilized eggs. After sexual maturity, sperm will be collected for cryopreservation.
Items: 1 to 6 of 6
1