At each time point after transplantation, TA muscles of the injected leg, the lung and liver were processed for cryosectioning as described for intramuscular transplantation.
Pieces of liver were processed using High Performance Liquid Chromatography (HPLC) with electrochemical detection for NA content according to our published method [28].
Vital organs (kidney and liver) were processed using a Citadel 1000 Histokinette (Shandon Scientific Ltd., Cheshire, UK).
Enzyme assays for liver were processed for enzyme activity within two weeks of homogenization.
Specimens from both the tibia and the liver were processed for light microscopic examination.
It seems that none of the fattened liver is processed in Chicago or even in Illinois.
The liver was processed for thick sections and evaluated after toludine blue staining and by electron microscopy after staining with uranyl acetate and lead citrate.
The remainder of the liver was processed for assay of microsomal enzyme activity.
All the rats were sacrificed after blood samples were taken for the measurements of aspartate aminotransferase (AST) and alanine aminotransferase (ALT) levels and liver was processed for conventional histopathology.
Plasma angiotensinogen (AGT, GenBank ID 183) synthesized by the liver is processed to angiotensin II (Ang II) by the serial action of renin and angiotensin-converting enzyme (ACE GenBank ID 1636).
