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Cspg4-P2A-CreERT2
製品ID :
I001152
系統:
C57BL/6JCya
状況:
説明:
The "Kozak-CreERT2-P2A" cassette was inserted upstream of the ATG start codon. CreERT2 recombinase is expressed under the regulatory control of Cspg4 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 Cspg4-positive cells (such as vascular pericytes and glial cells) following Tamoxifen induction.
The "Kozak-CreERT2-P2A" cassette was inserted upstream of the ATG start codon. CreERT2 recombinase is expressed under the regulatory control of Cspg4 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 Cspg4-positive cells (such as vascular pericytes and glial cells) following Tamoxifen induction.
Cspg4-flox
製品ID :
S-CKO-01415
系統:
C57BL/6JCya
状況:
説明:
Cspg4 is located on chromosome 9 of mice. SgRNA and ssDNA will be designed using Nuclease Technology; Cspg4 conditional knockout mice will be obtained by high-throughput electroporation of fertilized eggs. After sexual maturity, sperm will be collected for cryopreservation.
Cspg4 is located on chromosome 9 of mice. SgRNA and ssDNA will be designed using Nuclease Technology; Cspg4 conditional knockout mice will be obtained by high-throughput electroporation of fertilized eggs. After sexual maturity, sperm will be collected for cryopreservation.
Cspg4-KO
製品ID :
S-KO-17138
系統:
C57BL/6JCya
状況:
説明:
Cspg4 is located on chromosome 9 of mice. Nuclease Technology will be used to design sgRNA; Cspg4 knockout mice will be obtained by applying high-throughput electroporation of fertilized eggs. After sexual maturity, sperm were collected for cryopreservation.
Cspg4 is located on chromosome 9 of mice. Nuclease Technology will be used to design sgRNA; Cspg4 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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