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Models

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Mice

Rag2/Il2rg-KO/hSIRPA(BALB/c,2)

Strain Name:BALB/cAnSmoc-Sirpatm(hSIRPA)Rag2em1IL2rgem1Smoc
Strain State:Sperm cryopreservation | Cat. NO.:NM-KO-234081

On the basis of strain hSIRPA(BALB/c,2), Rag2 and Il2rg gene exon3 and Il2rg gene exon2 were knocked out to establish Rag2 and IL2RG gene knockout mouse models in hSIRPA(BALB/c,2) background.

Mice

Dsg1b-Flox

Strain Name:C57BL/6Smoc-Dsg1bem1(flox)Smoc
Strain State:Repository Live | Cat. NO.:NM-CKO-252691

These mice carry loxP sites flanking exon 7-11 of Dsg1b gene. When crossed with a Cre recombinase-expressing strain, this strain is useful in eliminating tissue-specific conditional expression of Dsg1b gene.After interacting with Cre, the overlapping gene lnc RNA ENSMUST00000365993 will be simultaneously knocked out.

Mice

Mt1-Flox/Mt2-Flox

Strain Name:C57BL/6Smoc-Mt1 em1(flox)Mt2 em1(flox)Smoc
Strain State:Repository Live | Cat. NO.:NM-CKO-252576

The MT1-FLOX model was constructed based on Mt2-Flox (NM-CKO-226357) by inserting loxP sites on both sides of exon 2-3 of the Mt1 gene respectively. This flox mouse can be mated with tissue-specific Cre tool mice to obtain mouse models with the Mt1 gene knocked out in specific cell types or tissues.

Mice

F9-KO

Strain Name:C57BL/6Smoc-F9em1Smoc
Strain State:Embryo cryopreservation | Cat. NO.:NM-KO-18046
Validation Data:Presence  |  Publications:1piece

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.

Mice

Fcgr2b-Fcgr3-Fcgr4-KO/hCTLA-4

Strain Name:C57BL/6Smoc-Fcgr2bem1Fcgr3em1Fcgr4em1Ctla4em1(hCTLA4)Smoc
Strain State:Sperm cryopreservation | Cat. NO.:NM-KO-220069

The Fcgr2b-Fcgr3-Fcgr4-KO/hCTLA4 mouse model was obtained by deleting all sequences from upstream of Fcgr3 gene to the 3'UTR of Fcgr2b gene in the hCTLA4(NM-HU-00014) mouse.

Mice

Fcgr2b-Fcgr3-Fcgr4-KO/hPD-1

Strain Name:C57BL/6Smoc-Fcgr2bem1Fcgr3em1Fcgr4em1Pdcd1em1(hPDCD1)Smoc
Strain State:Sperm cryopreservation | Cat. NO.:NM-KO-220068

The Fcgr2b-Fcgr3-Fcgr4-KO/hPD-1 mouse model was obtained by deleting all sequences from upstream of Fcgr3 gene to the 3'UTR of Fcgr2b gene in the hPD-1(NM-HU-00015) mouse.

Mice

Fcgr2b-Fcgr3-Fcgr4-KO/hPD-1/hCTLA-4

Strain Name:C57BL/6Smoc-Fcgr2bem1Fcgr3em1Fcgr4em1Pdcd1em1(hPDCD1)Ctla4em1(hCTLA4)Smoc
Strain State:Sperm cryopreservation | Cat. NO.:NM-KO-220070

The Fcgr2b-Fcgr3-Fcgr4-KO/hPD-1/hCTLA4 mouse model was obtained by deleting sequences from upstream of Fcgr3 gene to the 3'UTR of Fcgr2b gene in the hPD-1/hCTLA4(NM-HU-00079) mouse.

Mice

Ighm/Ighd-KO

Strain Name:C57BL/6Smoc-Ighmem1Ighdem1Smoc
Strain State:Repository Live | Cat. NO.:NM-KO-200610
Validation Data:Presence

Exon 1-6 of Ighm and exon 1-5 of Ighd gene was deleted to generate Ighm and Ighd knockout mice. Homozygous mutant mice lack mature B cells. It may be useful as a model for B cell immunodeficiency found in humans.

Mice

Bach1-Flox

Strain Name:C57BL/6Smoc-Bach1em2Smoc
Strain State:Sperm cryopreservation | Cat. NO.:NM-CKO-215033

These mice carry loxP sites flanking exon 2 of Bach1 gene. When crossed with a Cre recombinase-expressing strain, this strain is useful in eliminating tissue-specific conditional expression of this gene.

Mice

Gpr89/Prkab2-KO

Strain Name:C57BL/6Smoc-Gpr89em1Prkab2em1Smoc
Strain State:Embryo cryopreservation | Cat. NO.:NM-KO-18055

The sgRNAs were designed targeting Gpr89 intron11 and Prkab2 intron7 resulting in a sequence deletion of approximately 790 Kb between the Gpr89 gene and the Prkab2 gene.

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