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6 件の結果が “13807” で取得されました
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Eno2-P2A-iCre
製品ID :
C001577
系統:
C57BL/6JCya
状況:
説明:
The Eno2-P2A-iCre mouse was constructed by replacing the TGA stop codon of the endogenous mouse Eno2 gene with the P2A-iCre expression cassette. The expression pattern of the iCre recombinase (codon-optimized Cre recombinase) is similar to that of the mouse Eno2 gene. When Eno2-P2A-iCre mice are crossed with mice containing loxP sites, the offspring are expected to exhibit Cre recombinase-mediated sequence recombination between loxP sites in the nervous system (mature neurons).
The Eno2-P2A-iCre mouse was constructed by replacing the TGA stop codon of the endogenous mouse Eno2 gene with the P2A-iCre expression cassette. The expression pattern of the iCre recombinase (codon-optimized Cre recombinase) is similar to that of the mouse Eno2 gene. When Eno2-P2A-iCre mice are crossed with mice containing loxP sites, the offspring are expected to exhibit Cre recombinase-mediated sequence recombination between loxP sites in the nervous system (mature neurons).
Eno2-P2A-CreERT2
製品ID :
C001578
系統:
C57BL/6JCya
状況:
説明:
The Eno2-P2A-CreERT2 mouse was constructed by integrating the P2A-CreERT2 gene expression cassette into the mouse Eno2 gene using gene-editing technology, allowing for the expression of CreERT2 recombinase under the control of the mouse Eno2 gene regulatory elements. In the absence of tamoxifen treatment, CreERT2 recombinase is primarily located in the cytoplasm. Only under the action of tamoxifen can CreERT2 recombinase enter the nucleus and exert its recombination function. When Eno2-P2A-CreERT2 mice are crossed with mice containing loxP sites, tamoxifen induction is expected to trigger Cre recombinase-mediated sequence recombination between loxP sites in the nervous system (mature neurons) of the offspring.
The Eno2-P2A-CreERT2 mouse was constructed by integrating the P2A-CreERT2 gene expression cassette into the mouse Eno2 gene using gene-editing technology, allowing for the expression of CreERT2 recombinase under the control of the mouse Eno2 gene regulatory elements. In the absence of tamoxifen treatment, CreERT2 recombinase is primarily located in the cytoplasm. Only under the action of tamoxifen can CreERT2 recombinase enter the nucleus and exert its recombination function. When Eno2-P2A-CreERT2 mice are crossed with mice containing loxP sites, tamoxifen induction is expected to trigger Cre recombinase-mediated sequence recombination between loxP sites in the nervous system (mature neurons) of the offspring.
Rnf125-flox
製品ID :
S-CKO-13807
系統:
C57BL/6NCya
状況:
説明:
Rnf125 is located on chromosome 18 of mice. SgRNA and ssDNA were designed using Nuclease Technology; Rnf125 conditional knockout mice were obtained by high-throughput electroporation of fertilized eggs. After sexual maturity, sperm were collected for cryopreservation.
Rnf125 is located on chromosome 18 of mice. SgRNA and ssDNA were designed using Nuclease Technology; Rnf125 conditional knockout mice were obtained by high-throughput electroporation of fertilized eggs. After sexual maturity, sperm were collected for cryopreservation.
Eno2-KO
製品ID :
S-KO-01883
系統:
C57BL/6JCya
状況:
説明:
Eno2 is located on chromosome 6 of mice. Nuclease Technology was used to design sgRNA; Eno2 knockout mice were obtained by applying high-throughput electroporation of fertilized eggs. After sexual maturity, sperm were collected for cryopreservation.
Eno2 is located on chromosome 6 of mice. Nuclease Technology was used to design sgRNA; Eno2 knockout mice were obtained by applying high-throughput electroporation of fertilized eggs. After sexual maturity, sperm were collected for cryopreservation.
Eno2-flox
製品ID :
S-CKO-02205
系統:
C57BL/6NCya
状況:
説明:
Eno2 is located on chromosome 6 of mice. SgRNA and ssDNA were designed using Nuclease Technology; Eno2 conditional knockout mice were obtained by high-throughput electroporation of fertilized eggs. After sexual maturity, sperm were collected for cryopreservation.
Eno2 is located on chromosome 6 of mice. SgRNA and ssDNA were designed using Nuclease Technology; Eno2 conditional knockout mice were obtained by high-throughput electroporation of fertilized eggs. After sexual maturity, sperm were collected for cryopreservation.
Poglut2-KO
製品ID :
S-KO-13807
系統:
C57BL/6JCya
状況:
説明:
Poglut2 is located on chromosome 1 of mice. Nuclease Technology will be used to design sgRNA; Poglut2 knockout mice will be obtained by applying high-throughput electroporation of fertilized eggs. After sexual maturity, sperm were collected for cryopreservation.
Poglut2 is located on chromosome 1 of mice. Nuclease Technology will be used to design sgRNA; Poglut2 knockout mice will be obtained by applying high-throughput electroporation of fertilized eggs. After sexual maturity, sperm were collected for cryopreservation.
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