フィルター
5 件の結果が “18163” で取得されました
並べ替える:
アルファベット順（A-Z）
ベストセラー
Ctnnd2-tdTomato-loxP-Stop-loxP-DTR
製品ID :
C001751
系統:
C57BL/6JCya
状況:
説明:
The TAA stop codon was replaced with the P2A-tdTomato-IRES-loxP-6xSV40 pA loxP-DTR cassette. Upstream of the DTR (diphtheria toxin receptor) gene lies a loxP-Stop-loxP cassette that blocks DTR transcription and expression. In the absence of Cre recombinase, the Ctnnd2 promoter drives tdTomato expression, labeling Ctnnd2-positive cells with red fluorescence. Upon Cre recombination, Cre-mediated deletion of the loxP-flanked stop (LSL) element enables DTR expression in Cre-positive cells. Intravenous administration of diphtheria toxin (DT) then selectively ablates these cells.
The TAA stop codon was replaced with the P2A-tdTomato-IRES-loxP-6xSV40 pA loxP-DTR cassette. Upstream of the DTR (diphtheria toxin receptor) gene lies a loxP-Stop-loxP cassette that blocks DTR transcription and expression. In the absence of Cre recombinase, the Ctnnd2 promoter drives tdTomato expression, labeling Ctnnd2-positive cells with red fluorescence. Upon Cre recombination, Cre-mediated deletion of the loxP-flanked stop (LSL) element enables DTR expression in Cre-positive cells. Intravenous administration of diphtheria toxin (DT) then selectively ablates these cells.
Nol3-KO
製品ID :
S-KO-18163
系統:
C57BL/6JCya
状況:
説明:
Nol3 is located on chromosome 8 of mice. Nuclease Technology was used to design sgRNA; Nol3 knockout mice were obtained by applying high-throughput electroporation of fertilized eggs. After sexual maturity, sperm were collected for cryopreservation.
Nol3 is located on chromosome 8 of mice. Nuclease Technology was used to design sgRNA; Nol3 knockout mice were obtained by applying high-throughput electroporation of fertilized eggs. After sexual maturity, sperm were collected for cryopreservation.
Prlr-flox
製品ID :
S-CKO-18163
系統:
C57BL/6JCya
状況:
説明:
Prlr is located on chromosome 15 of mice. SgRNA and ssDNA will be designed using Nuclease Technology; Prlr conditional knockout mice will be obtained by high-throughput electroporation of fertilized eggs. After sexual maturity, sperm will be collected for cryopreservation.
Prlr is located on chromosome 15 of mice. SgRNA and ssDNA will be designed using Nuclease Technology; Prlr conditional knockout mice will be obtained by high-throughput electroporation of fertilized eggs. After sexual maturity, sperm will be collected for cryopreservation.
Ctnnd2-KO
製品ID :
S-KO-16053
系統:
C57BL/6JCya
状況:
説明:
Ctnnd2 is located on chromosome 15 of mice. Nuclease Technology was used to design sgRNA; Ctnnd2 knockout mice were obtained by applying high-throughput electroporation of fertilized eggs. After sexual maturity, sperm were collected for cryopreservation.
Ctnnd2 is located on chromosome 15 of mice. Nuclease Technology was used to design sgRNA; Ctnnd2 knockout mice were obtained by applying high-throughput electroporation of fertilized eggs. After sexual maturity, sperm were collected for cryopreservation.
Ctnnd2-flox
製品ID :
S-CKO-18388
系統:
C57BL/6JCya
状況:
説明:
Ctnnd2 is located on chromosome 15 of mice. SgRNA and ssDNA will be designed using Nuclease Technology; Ctnnd2 conditional knockout mice will be obtained by high-throughput electroporation of fertilized eggs. After sexual maturity, sperm will be collected for cryopreservation.
Ctnnd2 is located on chromosome 15 of mice. SgRNA and ssDNA will be designed using Nuclease Technology; Ctnnd2 conditional knockout mice will be obtained by high-throughput electroporation of fertilized eggs. After sexual maturity, sperm will be collected for cryopreservation.
Items: 1 to 5 of 5
1