1.CAMouseHG platform

 

Expresses human mouse chimeric IgM (Human Fv, mouse IgCμ and human light chain) and fully human IgG.

Human IgH heavy chain (hIgH) has 24 human variable-regions and all human D-regions and J-regions; mouse IgH 5’-enhance elements and mouse IgM (including Sμ, IgM (CH1, CH2, CH3 and CH4), TM1, TM2 and PolyA) are engineered for B-cell development and BCR signalling; human Igγ3 and Igγ1, and 3’-Locual control region are constructed for class switch and IgG production.  In particular, the replacement of human IgH 5’-enhancer and IgM with mouse IgH 5’-enhance elements and mouse IgM in the transgene promotes normal B-cell development, class-switch and hyper-mutation.

Human light chains (hIgK and hIgL) are composed of fully human immunoglobulin genomic segments.

Mouse endogenous IgH and IgK are inactivated.

 
2.CAMouseMG platform
 

Produces human and mouse chimeric IgM and IgG. Fc grafting in vitro to yield fully human antibody.

Transgenic IgH heavy chain (IgH) has 24 human variable-regions, all human D-regions and J-regions plus mouse C-region and mouse 3’-local control region.

Human light chains (hIgK and hIgL) transgenes are the same as CAMouseHG.

Mouse endogenous IgH and IgK are inactivated.
 
3. CAMouseH platform
 

Generates fully human heavy chain-only antibody (Igγ1-dCH1, Nanobody)

Human heavy chain-only IgH constitutes with 24 human variable-regions and all the human D-regions and J-regions, mouse IgH 5’-enhance elements and human Igγ1 [including mouse Sγ, human Igγ1 (Hinge, CH2 and CH3), mouse TM1, TM2 and PolyA] and mouse 3-Locual control region.  In particular, mouse enhancer and regulatory elements control human Igγ1-dCH1 expression, which promotes normal B-cell development and hyper-mutation.

Mouse endogenous IgH and IgK are inactivated.

 

 

 



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