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Models

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Mice

hNCR2

Strain Name:C57BL/6Smoc-Ncr1tm1(hNCR2 )Smoc
Strain State:Sperm cryopreservation | Cat. NO.:NM-HU-215068

The endogenous mouse Ncr1 gene was replaced by human NCR2 gene.

Mice

hSPN

Strain Name:C57BL/6Smoc-Spntm1(hSPN)Smoc
Strain State:Embryo cryopreservation | Cat. NO.:NM-HU-225032
Validation Data:Presence

The endogenous mouse Spn gene was replaced by human SPN gene.

Mice

hIL3

Strain Name:C57BL/6Smoc-Il3tm1(hIL3)Smoc
Strain State:Embryo cryopreservation | Cat. NO.:NM-HU-190009

The endogenous mouse Il3 gene was replaced by human IL3 gene.

Mice

hIL3/hCSF2

Strain Name:C57BL/6Smoc-Il3tm3(hIL3)Csf2tm3(hCSF2)/Smoc
Strain State:Embryo cryopreservation | Cat. NO.:NM-HU-190065
Validation Data:Presence

The endogenous mouse Il3 and Csf2 gene was replaced by human IL3 and CSF2 gene.

Mice

hIL4

Strain Name:C57BL/6Smoc-Il4tm3(hIL4)Smoc
Strain State:Embryo cryopreservation | Cat. NO.:NM-HU-190071
Validation Data:Presence

The endogenous mouse Il4 gene was completely or partially replaced by human IL4 gene via ESC targeting.

Mice

hADAM17

Strain Name:C57BL/6Smoc-Adam17tm(hADAM17)Smoc
Strain State:Developing | Cat. NO.:NM-HU-220260

The endogenous mouse Adam17 gene was replaced by human ADAM17 gene.

Mice

hLAIR1

Strain Name:C57BL/6Smoc-Lair1tm2(LAIR1)Smoc
Strain State:Embryo cryopreservation | Cat. NO.:NM-HU-2000011

The endogenous mouse Lair1 gene was replaced by human LAIR1 gene .

Mice

hNKG2A/hCD94

Strain Name:C57BL/6Smoc-Nkg2tm1(hNKG2A)Cd94tm1(hCD94)/Smoc
Strain State:Embryo cryopreservation | Cat. NO.:NM-HU-2000016

The endogenous mouse Nkg2 and Cd94 gene was replaced by human NKG2A and CD94 gene.

Mice

hIL4/hIL4R(BALB/c)

Strain Name:BALB/cAnSmoc-Il4tm3(hIL4)Il4ratm1(hIL4RA)Smoc
Strain State:Embryo cryopreservation | Cat. NO.:NM-HU-220167
Validation Data:Presence

The endogenous mouse Il4,Il4ra gene was replaced by human IL4 gene.

Mice

hAPP

Strain Name:C57BL/6Smoc-Apptm(hAPP)Smoc
Strain State:Sperm cryopreservation | Cat. NO.:NM-KI-220224

The endogenous mouse APP gene was replaced by human APP gene.

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