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4 件の結果が “12516” で取得されました
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Cd7-Furin-GSG-T2A-Dre
製品ID :
I001084
系統:
C57BL/6JCya
状況:
説明:
The TGA stop codon of the mouse Cd7 gene is replaced with Furin-GSG-T2A-Dre. The Furin sequence helps to remove the 2A residues from the upstream protein, while the GSG linkers can provide the necessary space to ensure proper protein folding and self-cleavage of the 2A sequence.
The TGA stop codon of the mouse Cd7 gene is replaced with Furin-GSG-T2A-Dre. The Furin sequence helps to remove the 2A residues from the upstream protein, while the GSG linkers can provide the necessary space to ensure proper protein folding and self-cleavage of the 2A sequence.
Cd7-KO
製品ID :
S-KO-01429
系統:
C57BL/6JCya
状況:
説明:
Cd7 is located on chromosome 11 of mice. Nuclease Technology was used to design sgRNA; Cd7 knockout mice were obtained by applying high-throughput electroporation of fertilized eggs. After sexual maturity, sperm were collected for cryopreservation.
Cd7 is located on chromosome 11 of mice. Nuclease Technology was used to design sgRNA; Cd7 knockout mice were obtained by applying high-throughput electroporation of fertilized eggs. After sexual maturity, sperm were collected for cryopreservation.
Cd7-flox
製品ID :
S-CKO-01638
系統:
C57BL/6JCya
状況:
説明:
Cd7 is located on chromosome 11 of mice. SgRNA and ssDNA will be designed using Nuclease Technology; Cd7 conditional knockout mice will be obtained by high-throughput electroporation of fertilized eggs. After sexual maturity, sperm will be collected for cryopreservation.
Cd7 is located on chromosome 11 of mice. SgRNA and ssDNA will be designed using Nuclease Technology; Cd7 conditional knockout mice will be obtained by high-throughput electroporation of fertilized eggs. After sexual maturity, sperm will be collected for cryopreservation.
Ppm1m-KO
製品ID :
S-KO-12516
系統:
C57BL/6JCya
状況:
説明:
Ppm1m is located on chromosome 9 of mice. Nuclease Technology will be used to design sgRNA; Ppm1m knockout mice will be obtained by applying high-throughput electroporation of fertilized eggs. After sexual maturity, sperm were collected for cryopreservation.
Ppm1m is located on chromosome 9 of mice. Nuclease Technology will be used to design sgRNA; Ppm1m 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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