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Drug-Resistant Variants of Escherichia coli Thymidylate Synthase
Drug-Resistant Variants of Escherichia coli Thymidylate Synthase

... Protein Purification. Cell free extracts were obtained from 2 g of wet cells by five 30-s consecutive sonication cycles (Branson Sonifier 450; Danbury, CT) in 25 ml of degassed QA buffer (50 mM Tris, 14 mM 2-mercaptoethanol, and 1 mM EDTA, pH 7.5), centrifuged at 11,000g for 30 min, and applied to a ...
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View Full PDF

... to two major fragments of 40 kDa and 27 kDa, corresponding to the enzymic core and to the hemopexin-like C-terminal domain respectively. By sequencing the N-terminus of each fragment, it was possible to deduce the autoproteolytic cleavage point, the peptide bond between either Gly242-Leu243 or Pro24 ...
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Ligand Conformation Enforces Trigonal

... the tripodal tetradentate amines have dramatic effects upon the structure, redox potential, and spectroscopic features of the corresponding complexes.25-27 Although important differences in the reactivity and properties of copper(II) complexes with tripodal N4 ligands can result from small changes i ...
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Ligand binding assay

Ligand Binding Assays (LBA) is an assay, or an analytic procedure, whose procedure or method relies on the binding of ligand molecules to receptors, antibodies or other macromolecules. A detection method is used to determine the presence and extent of the ligand-receptor complexes formed, and this is usually determined electrochemically or through a fluourescence method. This type of analytic test can be used to test for the presence of target molecules in a sample that are known to bind to the receptor.There are numerous types of ligand binding assays, both radioactive and non-radioactive. As such, ligand binding assays are a superset of radiobinding assays, which are the conceptual inverse of radioimmunoassays (RIA). Some newer types are called ""mix-and-measure"" assays because they do not require separation of bound ligands.Ligand binding assays are used primarily in pharmacology for various demands. Specifically, despite the human body’s endogenous receptors, hormones, and other neurotransmitters, pharmacologists utilize assays in order to create drugs that are selective, or mimic, the endogenously found cellular components. On the other hand, such techniques are also available to create receptor antagonists in order to prevent further cascades. Such advances provide researchers with the ability not only to quantify hormones and hormone receptors, but also to contribute important pharmacological information in drug development and treatment plans.
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