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Models

为您找到相关结果约86个
小鼠

Tacr1-CreERT2

品系名:C57BL/6Smoc-Tacr1em1(CreERT2-Wpre-pA)Smoc
品系状态:活体 | 目录号:NM-KI-200293

CreERT2-Wpre-pA expression cassette was knocked into the Tacr1 gene start codon site via CRISPR/Cas9 mediated recombination.

小鼠

Abcb1a/Abcb1b-KO(FVB)

品系名:FVB-Abcb1aem1Abcb1bem1Smoc
品系状态:活体 | 目录号:NM-KO-191211
验证数据:有

All sequences between exon2 of Abcb1a gene and exon28 of Abcb1b gene were knocked out by CRISPR/Cas9 technology.

小鼠

R26-CAG-LSL-Kras*G12C-IRES-Luc(BALB/c)

品系名:BALB/cAnSmoc-Gt(ROSA)26Sorem2(CAG-FRT-LSL-Kras(G12C)-IRES-Luciferase-polyA)Smoc
品系状态:精子冻存 | 目录号:NM-KI-200324

A CAG-FRT-loxp-stop-loxp-Kras(G12C)-IRES-Luciferase-polyA expression cassette was knocked into the R26 locus via CRISPR/Cas9 mediated recombination.

小鼠

R26-CAG-2xKRAB-dCas9-IRES-EGFP

品系名:C57BL/6Smoc-Gt(ROSA)26Sorem1(CAG-Loxp-2xKRAB-dCas9-IRES-EGFP)Smoc
品系状态:活体 | 目录号:NM-KI-18007
验证数据:有

These mice harbor a CAG-LSL-2xKRAB-dCas9-IRES-EGFP-WPRE-pA conditional expression cassette in mouse Rosa26 loci via homologous recombination. This strain can be used in CRISPR mediated target gene transcriptional inhibition (CRISPRi). The loxp-stop-loxp cassette was deleted.

小鼠

Tigre-pTRE2-LSL-ZGX!EmGFP-2A-ZGX!TagGFP2-2A-ZGX!hrGFP-CAG-LSL-tTA2

品系名:C57BL/6Smoc-Igs7em1(2Xlns-pTRE2-Lox2272-stop-Lox2272-ZGX!emGFP-T2A-ZGX!TagGFP2-P2A-ZGX!hrGFP-Wpre-pA-2Xlns-pCAG-LoxP-stop-LoxP-tTA2-Wpre-pA)Smoc
品系状态:胚胎冻存 | 目录号:NM-KI-200288

A 2Xlns-pTRE2-Lox2272-stop-Lox2272-ZGX!EmGFP-T2A-ZGX!TagGFP2-P2A-ZGX!hrGFP- Wpre-pA-2Xlns-pCAG-LoxP-stop-LoxP-tTA2-Wpre-pA expression cassette was knocked into the TIGRE locus via CRISPR/Cas9 mediated recombination.

小鼠

hHLA-E

品系名:C57BL/6Smoc-Igs2tm1(hHLA-E)Smoc
品系状态:胚胎冻存 | 目录号:NM-HU-200221

The endogenous human HLA-E gene (about 11kb) was knocked into the H11 locus via CRISPR/Cas9 mediated recombination.

小鼠

F9-KO

品系名:C57BL/6Smoc-F9em1Smoc
品系状态:胚胎冻存 | 目录号:NM-KO-18046
验证数据:有

The F9 gene is located on the X chromosome. In this F9 knockout mouse model, gRNAs were designed targeting Exon8 of F9 gene via CRISPR gene editing technology. Loss of F9 caused coagulopathy in mice. Mice that are homozygous for F9 knockout are viable, fertile and normal in size. Normal fighting in the cage may cause bleeding or even death due to massive internal hemorrhaging. After the tail cutting, wounds must be cauterized to prevent homozygous knockout mice from blood loss and death. This strain is a powerful model for studying coagulopathy, gene therapy methods and function of factor IX mutations. F9-KO mice (Stock No.NM-KO-18046)carry a knockout allele derived from the targeted deletion of exon 8. While F9-KO(2) mice (Stock No.NM-KO-200607) carrying the exon 1-8 deletion.

小鼠

Rps4l-Flox(AI)

品系名:C57BL/6Smoc-Rps4lem2(flox)Smoc
品系状态:活体 | 目录号:NM-CKO-242022

The artificial intron was knocked into the Rps4l gene exon 1. When crossed with a Cre recombinase-expressing strain, this strain is useful in eliminating tissue-specific conditional expression of Rps4l gene. Construction strategy References CRISPR-Cas9-mediated insertion of a short artificial intron for the generation of conditional alleles in mice.

大鼠

Foxn1-KO(SD)

品系名:SD-Foxn1em1Smoc 品系状态:胚胎冻存 | 目录号:NR-KO-190002

Using CRISPR/Cas9 technology, Exon 2-4 of Foxn1 gene was deleted to generate Foxn1 knockout rat.

大鼠

F8-KO(SD)

品系名:SD-F8em1Smoc 品系状态:活体 | 目录号:NR-KO-200003
验证数据:有

Using CRISPR/Cas9 technology, exon 16 of F8 gene was deleted to generate F8 knockout rat.

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