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Gfi1-EGFP-CreERT2
製品ID :
C001753
系統:
C57BL/6JCya
状況:
説明:
The TGA stop codon was replaced with the P2A-EGFP-CreERT2 cassette. CreERT2 recombinase and enhanced green fluorescent protein (EGFP) are expressed under the regulatory control of Gfi1 gene elements. This model is a Tamoxifen-inducible Cre mouse, and when crossed with mice containing loxP sites, the offspring mice are expected to undergo sequence recombination between loxP sites mediated by Cre recombinase in Gfi1-positive cells following Tamoxifen induction. In addition to studies of Cre recombinase-mediated gene recombination, this model can also be used for EGFP fluorescent protein tracing studies.
The TGA stop codon was replaced with the P2A-EGFP-CreERT2 cassette. CreERT2 recombinase and enhanced green fluorescent protein (EGFP) are expressed under the regulatory control of Gfi1 gene elements. This model is a Tamoxifen-inducible Cre mouse, and when crossed with mice containing loxP sites, the offspring mice are expected to undergo sequence recombination between loxP sites mediated by Cre recombinase in Gfi1-positive cells following Tamoxifen induction. In addition to studies of Cre recombinase-mediated gene recombination, this model can also be used for EGFP fluorescent protein tracing studies.
Gpx8-flox
製品ID :
S-CKO-14581
系統:
C57BL/6JCya
状況:
説明:
Gpx8 is located on chromosome 13 of mice. SgRNA and ssDNA were designed using Nuclease Technology; Gpx8 conditional knockout mice were obtained by high-throughput electroporation of fertilized eggs. After sexual maturity, sperm were collected for cryopreservation.
Gpx8 is located on chromosome 13 of mice. SgRNA and ssDNA were designed using Nuclease Technology; Gpx8 conditional knockout mice were obtained by high-throughput electroporation of fertilized eggs. After sexual maturity, sperm were collected for cryopreservation.
Sv2c-KO
製品ID :
S-KO-14581
系統:
C57BL/6JCya
状況:
説明:
Sv2c is located on chromosome 13 of mice. Nuclease Technology was used to design sgRNA; Sv2c knockout mice were obtained by applying high-throughput electroporation of fertilized eggs. After sexual maturity, sperm were collected for cryopreservation.
Sv2c is located on chromosome 13 of mice. Nuclease Technology was used to design sgRNA; Sv2c knockout mice were obtained by applying high-throughput electroporation of fertilized eggs. After sexual maturity, sperm were collected for cryopreservation.
Gfi1-KO
製品ID :
S-KO-18059
系統:
C57BL/6JCya
状況:
説明:
Gfi1 is located on chromosome 5 of mice. Nuclease Technology was used to design sgRNA; Gfi1 knockout mice were obtained by applying high-throughput electroporation of fertilized eggs. After sexual maturity, sperm were collected for cryopreservation.
Gfi1 is located on chromosome 5 of mice. Nuclease Technology was used to design sgRNA; Gfi1 knockout mice were obtained by applying high-throughput electroporation of fertilized eggs. After sexual maturity, sperm were collected for cryopreservation.
Gfi1-flox
製品ID :
S-CKO-02611
系統:
C57BL/6NCya
状況:
説明:
Gfi1 is located on chromosome 5 of mice. SgRNA and ssDNA were designed using Nuclease Technology; Gfi1 conditional knockout mice were obtained by high-throughput electroporation of fertilized eggs. After sexual maturity, sperm were collected for cryopreservation.
Gfi1 is located on chromosome 5 of mice. SgRNA and ssDNA were designed using Nuclease Technology; Gfi1 conditional knockout mice were obtained by high-throughput electroporation of fertilized eggs. After sexual maturity, sperm were collected for cryopreservation.
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