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5 件の結果が “22287” で取得されました
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Scgb1a1-iCre
製品ID :
I001145
系統:
C57BL/6JCya
状況:
説明:
The TGA stop codon was replaced with the "P2A-iCre" cassette. Cre recombinase is expressed under the regulatory control of Scgb1a1 gene elements.
The TGA stop codon was replaced with the "P2A-iCre" cassette. Cre recombinase is expressed under the regulatory control of Scgb1a1 gene elements.
Scgb1a1-P2A-CreERT2
製品ID :
C001581
系統:
C57BL/6JCya
状況:
説明:
The Scgb1a1-P2A-CreERT2 mouse was constructed by integrating the P2A-CreERT2 gene expression cassette into the mouse Scgb1a1 gene using gene-editing technology, allowing for the expression of CreERT2 recombinase under the control of the mouse Scgb1a1 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 Scgb1a1-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 bronchial and alveolar epithelial cells of the offspring.
The Scgb1a1-P2A-CreERT2 mouse was constructed by integrating the P2A-CreERT2 gene expression cassette into the mouse Scgb1a1 gene using gene-editing technology, allowing for the expression of CreERT2 recombinase under the control of the mouse Scgb1a1 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 Scgb1a1-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 bronchial and alveolar epithelial cells of the offspring.
Foxg1-flox
製品ID :
S-CKO-22287
系統:
C57BL/6JCya
状況:
説明:
Foxg1 is located on chromosome 12 of mice. SgRNA and ssDNA will be designed using Nuclease Technology; Foxg1 conditional knockout mice will be obtained by high-throughput electroporation of fertilized eggs. After sexual maturity, sperm will be collected for cryopreservation.
Foxg1 is located on chromosome 12 of mice. SgRNA and ssDNA will be designed using Nuclease Technology; Foxg1 conditional knockout mice will be obtained by high-throughput electroporation of fertilized eggs. After sexual maturity, sperm will be collected for cryopreservation.
Scgb1a1-KO
製品ID :
S-KO-05662
系統:
C57BL/6JCya
状況:
説明:
Scgb1a1 is located on chromosome 19 of mice. Nuclease Technology was used to design sgRNA; Scgb1a1 knockout mice were obtained by applying high-throughput electroporation of fertilized eggs. After sexual maturity, sperm were collected for cryopreservation.
Scgb1a1 is located on chromosome 19 of mice. Nuclease Technology was used to design sgRNA; Scgb1a1 knockout mice were obtained by applying high-throughput electroporation of fertilized eggs. After sexual maturity, sperm were collected for cryopreservation.
Scgb1a1-flox
製品ID :
S-CKO-06565
系統:
C57BL/6JCya
状況:
説明:
Scgb1a1 is located on chromosome 19 of mice. SgRNA and ssDNA were designed using Nuclease Technology; Scgb1a1 conditional knockout mice were obtained by high-throughput electroporation of fertilized eggs. After sexual maturity, sperm were collected for cryopreservation.
Scgb1a1 is located on chromosome 19 of mice. SgRNA and ssDNA were designed using Nuclease Technology; Scgb1a1 conditional knockout mice were obtained by high-throughput electroporation of fertilized eggs. After sexual maturity, sperm were collected for cryopreservation.
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