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6 件の結果が “22227” で取得されました
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Ucp1-P2A-Cre
製品ID :
I001104
系統:
C57BL/6JCya
状況:
説明:
The TAA stop codon of the mouse Ucp1 gene is replaced with the P2A-Cre gene expression cassette through gene-editing technology. When Ucp1-P2A-Cre mice are crossed with mice containing loxP sites, it is expected that Cre-recombinase-mediated sequence recombination between loxP sites can be triggered in the brown fat of the offspring.
The TAA stop codon of the mouse Ucp1 gene is replaced with the P2A-Cre gene expression cassette through gene-editing technology. When Ucp1-P2A-Cre mice are crossed with mice containing loxP sites, it is expected that Cre-recombinase-mediated sequence recombination between loxP sites can be triggered in the brown fat of the offspring.
Btnl9-KO
製品ID :
S-KO-22227
系統:
C57BL/6JCya
状況:
説明:
Btnl9 is located on chromosome 11 of mice. Nuclease Technology was used to design sgRNA; Btnl9 knockout mice were obtained by applying high-throughput electroporation of fertilized eggs. After sexual maturity, sperm were collected for cryopreservation.
Btnl9 is located on chromosome 11 of mice. Nuclease Technology was used to design sgRNA; Btnl9 knockout mice were obtained by applying high-throughput electroporation of fertilized eggs. After sexual maturity, sperm were collected for cryopreservation.
Mpdz-flox
製品ID :
S-CKO-22227
系統:
C57BL/6JCya
状況:
説明:
Mpdz is located on chromosome 4 of mice. SgRNA and ssDNA will be designed using Nuclease Technology; Mpdz conditional knockout mice will be obtained by high-throughput electroporation of fertilized eggs. After sexual maturity, sperm will be collected for cryopreservation.
Mpdz is located on chromosome 4 of mice. SgRNA and ssDNA will be designed using Nuclease Technology; Mpdz conditional knockout mice will be obtained by high-throughput electroporation of fertilized eggs. After sexual maturity, sperm will be collected for cryopreservation.
Ucp1-KO
製品ID :
S-KO-05629
系統:
C57BL/6JCya
状況:
説明:
Ucp1 is located on chromosome 8 of mice. Nuclease Technology was used to design sgRNA; Ucp1 knockout mice were obtained by applying high-throughput electroporation of fertilized eggs. After sexual maturity, sperm were collected for cryopreservation.
Ucp1 is located on chromosome 8 of mice. Nuclease Technology was used to design sgRNA; Ucp1 knockout mice were obtained by applying high-throughput electroporation of fertilized eggs. After sexual maturity, sperm were collected for cryopreservation.
Ucp1-KO
製品ID :
S-KO-05628
系統:
C57BL/6NCya
状況:
説明:
Ucp1 is located on chromosome 8 of mice. Nuclease Technology was used to design sgRNA; Ucp1 knockout mice were obtained by applying high-throughput electroporation of fertilized eggs. After sexual maturity, sperm were collected for cryopreservation.
Ucp1 is located on chromosome 8 of mice. Nuclease Technology was used to design sgRNA; Ucp1 knockout mice were obtained by applying high-throughput electroporation of fertilized eggs. After sexual maturity, sperm were collected for cryopreservation.
Ucp1-flox
製品ID :
S-CKO-06528
系統:
C57BL/6JCya
状況:
説明:
Ucp1 is located on chromosome 8 of mice. SgRNA and ssDNA were designed using Nuclease Technology; Ucp1 conditional knockout mice were obtained by high-throughput electroporation of fertilized eggs. After sexual maturity, sperm were collected for cryopreservation.
Ucp1 is located on chromosome 8 of mice. SgRNA and ssDNA were designed using Nuclease Technology; Ucp1 conditional knockout mice were obtained by high-throughput electroporation of fertilized eggs. After sexual maturity, sperm were collected for cryopreservation.
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