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4 件の結果が “20606” で取得されました
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H11-Sstr2-Cre
製品ID :
I001069
系統:
C57BL/6JCya
状況:
説明:
For the Kl model, the Sstr2 promoter-Kozak-Cre-rBG pA cassette will be inserted into the H11 locus (~0.7 kb 5'of Eif4enif1 gene and ~4.5 kb 3' of the Drg1 gene). This model expresses Cre recombinase under the drive of the mouse Sstr2 promoter.
For the Kl model, the Sstr2 promoter-Kozak-Cre-rBG pA cassette will be inserted into the H11 locus (~0.7 kb 5'of Eif4enif1 gene and ~4.5 kb 3' of the Drg1 gene). This model expresses Cre recombinase under the drive of the mouse Sstr2 promoter.
F2-KO
製品ID :
S-KO-20606
系統:
C57BL/6JCya
状況:
説明:
F2 is located on chromosome 2 of mice. Nuclease Technology was used to design sgRNA; F2 knockout mice were obtained by applying high-throughput electroporation of fertilized eggs. After sexual maturity, sperm were collected for cryopreservation.
F2 is located on chromosome 2 of mice. Nuclease Technology was used to design sgRNA; F2 knockout mice were obtained by applying high-throughput electroporation of fertilized eggs. After sexual maturity, sperm were collected for cryopreservation.
Sstr2-KO
製品ID :
S-KO-04391
系統:
C57BL/6JCya
状況:
説明:
Sstr2 is located on chromosome 11 of mice. Nuclease Technology will be used to design sgRNA; Sstr2 knockout mice will be obtained by applying high-throughput electroporation of fertilized eggs. After sexual maturity, sperm were collected for cryopreservation.
Sstr2 is located on chromosome 11 of mice. Nuclease Technology will be used to design sgRNA; Sstr2 knockout mice will be obtained by applying high-throughput electroporation of fertilized eggs. After sexual maturity, sperm were collected for cryopreservation.
Sstr2-flox
製品ID :
S-CKO-20165
系統:
C57BL/6JCya
状況:
説明:
Sstr2 is located on chromosome 11 of mice. SgRNA and ssDNA will be designed using Nuclease Technology; Sstr2 conditional knockout mice will be obtained by high-throughput electroporation of fertilized eggs. After sexual maturity, sperm will be collected for cryopreservation.
Sstr2 is located on chromosome 11 of mice. SgRNA and ssDNA will be designed using Nuclease Technology; Sstr2 conditional knockout mice will be obtained by high-throughput electroporation of fertilized eggs. After sexual maturity, sperm will be collected for cryopreservation.
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