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The influence of mouse sera, regenerating liver extracts and bacterial products on the abilities of different cells in vitro

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Academic year: 2020

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Figure

Fig. 2 Numbersof HEp-2 cells followingcultivationIn mediumwithteta/calfserum(FCS). normalmouseserum(NMS),sham-hepatectomizedmouseserum(SHMSJ,parriallyhepatectomizedmouseserum(PHMSJ.normalmousefivere;to,tract (NLEJ,sham-hepatectomizedmouseliverextract(SHLEJ.partially hepatectomizedmouseliver extract(PHLEJor inmediumsupplementedwith an adequatevolumeof saline(SI), respectively.
Fig.3.HEp-2cellscultivatedin mediumsupplemenredwithferal calf serum IA)orwithnormal mouse serum181
Fig. 4. Numbersserum (FCS),normalserummouse liver e,<tract(NMLEJ,sham-hepatecromlzed mousesupplemented withof murine fetal cells followingcultivationwith fetal calf mouse serum (NMS),sham-hepatectomized mouse(SHMS).partiallyhepatecromlzed mouse serum (PHMS),normalliverextract(SHLEJ, parrialfy hepatectomizedmouseliver extract (PHLEJ, orin medium an adequate volume of saline (SI), respectively.
Fig. 6Numbersof particularbacterialcoloniesperplatefollowingplatingwith the extractsfrom normal mouseliver(NLE),sham-hepatectomizedmouseliver extract(SHLE), partially hepatectomizedmouseliverextract(PHLEJ.or in mediumsupplementedwith an adequatevolumeof saline (51), respectively.
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