Transgenic animals

Tissue and cell metabolism

Animal metabolism can be screened in homogenates or extracts of frozen tissues (e.g.brain, heart, liver, kidney, skeletal muscle, and gonads) by photometric or fluorimetric analyses of key enzymes and central metabolites.
The physiological capacities of the different metabolic pathways are determined by measuring the maximal catalytic activities of key enzymes (maximal velocity, Vmax under standard conditions). The actual situation of metabolism is described by the composition of macromolecules and the concentrations of central metabolites.
You will receive a detailed protocol of measurement and our physiological interpretation of the data. We recommend a comparative analysis of transgenic animals with controls of the same age and sex.

Compact Tissue Profile of Catabolic Capacity

Catabolic processes are essential for delivering energy in form of ATP. The tissue profile of catabolism analyses the major fuel utilization pathways.

Compact tissue Profile of Anabolic Capacity

The synthesis of complex molecules is the essential feature of anabolism. Our tissue profile offers a compact view in efficiency of molecule synthesis.

Comprehensive Tissue Profile of Metabolic Capacity

Our comprehensive tissue profile offers an in-depth analysis of catabolic and anabolic pathways.

Tissue Profile of Macromolecules and Central Metabolites

Metabolite concentrations represent the actual situation of tissue metabolism. Rapid freezing of tissues is necessary for physiological interpretation of the data. This profile screens the chemical composition of the tissue and can visualize defects of metabolism (e.g. obesity, diabetes, tumors, muscle fatique).

Tissue Profile of Antioxidant Network

Oxygen metabolism is accompanied by the production of oxidants (e.g. radicals) which detoxification is important for aerobic tissues. This tissue profile offers analysis of enzymes involved in pathways of the antioxidant network.

Tissue Profile of Shuttle Systems

Certain metabolites are transported inside the cells by enzymatic shuttle systems. The ratio of the contributed enzyme forms is determined.