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Ntrk1-CreERT2
製品ID :
C001760
系統:
C57BL/6JCya
状況:
説明:
Ntrk1-CreERT2 mice are generated by inserting an IRES-CreERT2 cassette via genome editing immediately downstream of the TAG stop codon in the mouse Ntrk1 gene. Without tamoxifen treatment, CreERT2 recombinase primarily resides in the cytoplasm; nuclear translocation and recombination activity of CreERT2 only occur upon tamoxifen stimulation. When crossed with mice containing loxP sites, offspring are expected to exhibit Cre-mediated recombination between loxP sites in Ntrk1-positive cells following tamoxifen administration.
Ntrk1-CreERT2 mice are generated by inserting an IRES-CreERT2 cassette via genome editing immediately downstream of the TAG stop codon in the mouse Ntrk1 gene. Without tamoxifen treatment, CreERT2 recombinase primarily resides in the cytoplasm; nuclear translocation and recombination activity of CreERT2 only occur upon tamoxifen stimulation. When crossed with mice containing loxP sites, offspring are expected to exhibit Cre-mediated recombination between loxP sites in Ntrk1-positive cells following tamoxifen administration.
Eml2-KO
製品ID :
S-KO-18211
系統:
C57BL/6JCya
状況:
説明:
Eml2 is located on chromosome 7 of mice. Nuclease Technology was used to design sgRNA; Eml2 knockout mice were obtained by applying high-throughput electroporation of fertilized eggs. After sexual maturity, sperm were collected for cryopreservation.
Eml2 is located on chromosome 7 of mice. Nuclease Technology was used to design sgRNA; Eml2 knockout mice were obtained by applying high-throughput electroporation of fertilized eggs. After sexual maturity, sperm were collected for cryopreservation.
Pycr1-flox
製品ID :
S-CKO-18211
系統:
C57BL/6JCya
状況:
説明:
Pycr1 is located on chromosome 11 of mice. SgRNA and ssDNA were designed using Nuclease Technology; Pycr1 conditional knockout mice were obtained by high-throughput electroporation of fertilized eggs. After sexual maturity, sperm were collected for cryopreservation.
Pycr1 is located on chromosome 11 of mice. SgRNA and ssDNA were designed using Nuclease Technology; Pycr1 conditional knockout mice were obtained by high-throughput electroporation of fertilized eggs. After sexual maturity, sperm were collected for cryopreservation.
Ntrk1-KO
製品ID :
S-KO-03446
系統:
C57BL/6JCya
状況:
説明:
Ntrk1 is located on chromosome 3 of mice. Nuclease Technology was used to design sgRNA; Ntrk1 knockout mice were obtained by applying high-throughput electroporation of fertilized eggs. After sexual maturity, sperm were collected for cryopreservation.
Ntrk1 is located on chromosome 3 of mice. Nuclease Technology was used to design sgRNA; Ntrk1 knockout mice were obtained by applying high-throughput electroporation of fertilized eggs. After sexual maturity, sperm were collected for cryopreservation.
Ntrk1-flox
製品ID :
S-CKO-04044
系統:
C57BL/6JCya
状況:
説明:
Ntrk1 is located on chromosome 3 of mice. SgRNA and ssDNA were designed using Nuclease Technology; Ntrk1 conditional knockout mice were obtained by high-throughput electroporation of fertilized eggs. After sexual maturity, sperm were collected for cryopreservation.
Ntrk1 is located on chromosome 3 of mice. SgRNA and ssDNA were designed using Nuclease Technology; Ntrk1 conditional knockout mice were obtained by high-throughput electroporation of fertilized eggs. After sexual maturity, sperm were collected for cryopreservation.
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