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Gigantic Poster for Studying Over 100 Inborn Metabolic Errors and Their Genes

Download, Explore Online or Order Printed Copy from Merck and Hang on Lab Wall

Inborn Errors Poster

Detail: Lipid Biosynthesis

Detail: Purines Pyrimidines

Use this large-format map to quickly reference over 100 metabolic deficiency diseases. Metabolomics research labs, educational institutions, lecturers, and students will all find this map helpful in tracing enzymatic activity to diseases in the body.

Every characteristic of human anatomy and physiology is determined by biochemical reactions and catalyzed by enzymes. The enzymes are determined by our genetic make-up. If a gene is defective or missing, it will result in a defective or missing enzyme, a so-called "inborn error of metabolism." Knowledge of the defective enzyme and its gene or genes may well make possible the rational treatment of the resulting disease. The Inborn Errors of Metabolism Map identifies the site of over 100 metabolic deficiency diseases that are named on the sides of the map.

The map is based on the glycolytic pathway followed by the the tricarboxylic acid (TCA) or Krebs cycle and the respiratory chain. Together these paths lead to the synthesis of adenosine triphosphate (ATP), the source of most of the energy required for all life, via ATP synthase. Many biosynthetic and breakdown pathways of metabolism such as those concerning carbohydrates, amino acids, and lipids are associated with this pathway and are differentiated by differences in color. Human metabolism is distinguished, where possible, by the use of black arrows.  

Download the file or order the 84 cm x 127 cm poster to hang on your laboratory wall!

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We are happy to answer your questions by phone at +49 (0) 6151 276 46 62


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