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Models

About 84 results
Mice

Apob-Q1388H

Strain Name：C57BL/6Smoc-Apobem1(Q1388H)Smoc
Strain State：Embryo cryopreservation | Cat. NO.：NM-KI-00056

These mice carry a c.g4164t mutation in Apob gene via CRISPR/Cas mediated recombination.

Mice

Atp7b-H1071Q

Strain Name：C57BL/6Smoc-Atp7bem1(H1071Q)Smoc
Strain State：Embryo cryopreservation | Cat. NO.：NM-KI-18001

These mice carry a p.H1071Q mutation in exon14 of Atp7b gene.

Mice

Akt1-C224S

Strain Name：C57BL/6Smoc-Akt1em(C224S)Smoc
Strain State：Embryo cryopreservation | Cat. NO.：NM-KI-215096

These mice carry a C224S mutation of Akt1 gene.

Mice

Zbtb46-T11A

Strain Name：C57BL/6Smoc-Zbtb46em(T11A)Smoc
Strain State：Embryo cryopreservation | Cat. NO.：NM-KI-215097

These mice carry a T11A mutation of Zbtb46 gene.

Mice

Mdm4-C462A

Strain Name：B6;129S-Mdm4tm1Smoc
Strain State：Embryo cryopreservation | Cat. NO.：NM-KI-00007

A point mutant at exon 12 was recombined to create a Mdm4 gene mutant mice.

Mice

Trem2-R47H

Strain Name：C57BL/6Smoc-Trem2em3(p.R47H)Smoc
Strain State：Embryo cryopreservation | Cat. NO.：NM-KI-190092

These mice carry a p.R47H mutation of Trem2 gene.

Mice

Npc1-I1060T

Strain Name：C57BL/6Smoc-Npc1em1(I1060T)Smoc
Strain State：Embryo cryopreservation | Cat. NO.：NM-KI-18059

The I1060T point mutation is located in exon21 of mouse Npc1 gene. This Npc1 point mutation mouse model was established by introduce a T>C transversion at the 138th nucleotide of exon21.

Mice

Gba-D427V

Strain Name：C57BL/6Smoc-Gbaem1(D427v)Smoc
Strain State：Repository Live | Cat. NO.：NM-KI-18060

The D427V point mutation is located in exon9 of mouse Gba gene. This Gba point mutation mouse model was established by introduce an A>T transversion at the 119th nucleotide of exon9.

Mice

Mapt-R5H

Strain Name：C57BL/6Smoc-Maptem(R5H)Smoc
Strain State：Sperm cryopreservation | Cat. NO.：NM-KI-215099

These mice carry a R5H mutation of Mapt gene.

Mice

Trpm2-D1066A

Strain Name：C57BL/6Smoc-Trpm2em(D1066A)Smoc
Strain State：Sperm cryopreservation | Cat. NO.：NM-KI-215101

These mice carry a D1066A mutation of Trpm2 gene.

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