By Michael J. Groves

ISBN-10: 0849318734

ISBN-13: 9780849318733

Because the book of the 1st variation of Pharmaceutical Biotechnology over a decade in the past, a not-so-subtle shift within the which means of the time period "biotechnology" has happened. It has come to intend whatever very particular, particularly the improvement of drug ingredients with huge protein and polypeptide molecules. those components can be utilized as medicinal drugs of their personal correct yet can also be used to control mobile DNA with a view to produce a required molecule that's believed to have fascinating homes within the therapy of a illness. for this reason, the second one version of this well known textual content displays that modify of definition via together with new fabric that explores the advance of those protein-based healing ingredients. See what is new within the moment variation:

  • Expanded insurance of the formula of proteins
  • Additional info on proteins used as drug supply structures
  • Detailed dialogue of interactions among proteins and phospholipids
  • Increased details on proteomics and gene treatment
  • Exploration of pulmonary management and oral supply of proteins
  • A huge evaluate of vaccines
  • Discussion of genetic engineering and genomics
  • Challenges and concerns concerned with the advance and the creation of a drug
  • Show description

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    Extra info for Pharmaceutical Biotechnology

    Example text

    With PCR, one can amplify the desired DNA sequence to the point where the rest of the DNA can be ignored, and so the viral gene’s presence can be easily detected, for example, by using a hybridization assay. To do this, one must first chemically synthesize two sets of DNA oligomers to use as primers for DNA polymerase. The sequence of each of the primers is carefully chosen to match the viral DNA sequence just within—or just outside, if possible— the gene of interest, one primer for each end of the gene.

    Polarization interactions for atoms and small molecules or functional groups are much weaker than the other interactions listed above. 4 nm. , a protein binding a large substrate molecule) the overall contribution may be 10 to 20 kcal/mol (40–80 kJ/mol). Furthermore, these interactions will be present for both nonpolar and polar (even ionic) groups. THE HYDROPHOBIC EFFECT Nonpolar molecules tend to have low solubilities in water, and large nonpolar solutes tend to form aggregates in aqueous solution.

    1), while a purified DNA sample whose molecules are all of the same length will show only one band. In a typical experimental setup, the agarose or polyacrylamide is cast as a slab (a slab gel); the slab may be cast vertically, between two glass plates, or (for agarose but not polyacrylamide) it may be cast horizontally onto a single plate. Before the gel is actually poured for casting, a plastic template with multiple teeth, which resembles a coarse comb, is inserted at the top of the slab. This is done so that the solidified gel will keep the impression of those teeth as a series of indentations or wells that can hold individual DNA samples.

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    Pharmaceutical Biotechnology by Michael J. Groves

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