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5 件の結果が “18189” で取得されました
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Nrxn1-CreERT2-P2A-Superfolder GFP
製品ID :
I001096
系統:
C57BL/6JCya
状況:
説明:
The partial coding sequence of exon 2 of the mouse Nrxn1 gene is replaced by CreERT2-P2A-Superfolder GFP-WPRE-rBG pA. When this strain is crossed with mice containing loxP sites, after tamoxifen induction in the offspring mice, it is expected to trigger Cre-recombinase-mediated sequence recombination between loxP sites in neurexin-1 neurons. In addition, a green fluorescent protein (GFP) expression element is inserted after the CreERT2 recombinase element in this model, which can also be used for the tracking of Nrxn1-positive cells.
The partial coding sequence of exon 2 of the mouse Nrxn1 gene is replaced by CreERT2-P2A-Superfolder GFP-WPRE-rBG pA. When this strain is crossed with mice containing loxP sites, after tamoxifen induction in the offspring mice, it is expected to trigger Cre-recombinase-mediated sequence recombination between loxP sites in neurexin-1 neurons. In addition, a green fluorescent protein (GFP) expression element is inserted after the CreERT2 recombinase element in this model, which can also be used for the tracking of Nrxn1-positive cells.
Tmem39a-flox
製品ID :
S-CKO-18189
系統:
C57BL/6JCya
状況:
説明:
Tmem39a is located on chromosome 16 of mice. SgRNA and ssDNA will be designed using Nuclease Technology; Tmem39a conditional knockout mice will be obtained by high-throughput electroporation of fertilized eggs. After sexual maturity, sperm will be collected for cryopreservation.
Tmem39a is located on chromosome 16 of mice. SgRNA and ssDNA will be designed using Nuclease Technology; Tmem39a conditional knockout mice will be obtained by high-throughput electroporation of fertilized eggs. After sexual maturity, sperm will be collected for cryopreservation.
Cntn6-KO
製品ID :
S-KO-18189
系統:
C57BL/6JCya
状況:
説明:
Cntn6 is located on chromosome 6 of mice. Nuclease Technology was used to design sgRNA; Cntn6 knockout mice were obtained by applying high-throughput electroporation of fertilized eggs. After sexual maturity, sperm were collected for cryopreservation.
Cntn6 is located on chromosome 6 of mice. Nuclease Technology was used to design sgRNA; Cntn6 knockout mice were obtained by applying high-throughput electroporation of fertilized eggs. After sexual maturity, sperm were collected for cryopreservation.
Nrxn1-KO
製品ID :
S-KO-03438
系統:
C57BL/6JCya
状況:
説明:
Nrxn1 is located on chromosome 17 of mice. Nuclease Technology was used to design sgRNA; Nrxn1 knockout mice were obtained by applying high-throughput electroporation of fertilized eggs. After sexual maturity, sperm were collected for cryopreservation.
Nrxn1 is located on chromosome 17 of mice. Nuclease Technology was used to design sgRNA; Nrxn1 knockout mice were obtained by applying high-throughput electroporation of fertilized eggs. After sexual maturity, sperm were collected for cryopreservation.
Nrxn1-flox
製品ID :
S-CKO-19578
系統:
C57BL/6JCya
状況:
説明:
Nrxn1 is located on chromosome 17 of mice. SgRNA and ssDNA were designed using Nuclease Technology; Nrxn1 conditional knockout mice were obtained by high-throughput electroporation of fertilized eggs. After sexual maturity, sperm were collected for cryopreservation.
Nrxn1 is located on chromosome 17 of mice. SgRNA and ssDNA were designed using Nuclease Technology; Nrxn1 conditional knockout mice were obtained by high-throughput electroporation of fertilized eggs. After sexual maturity, sperm were collected for cryopreservation.
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