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Example of a T-REx system controlling the expression of shRNA. Tetracycline-controlled transcriptional activation is a method of inducible gene expression where transcription is reversibly turned on or off in the presence of the antibiotic tetracycline or one of its derivatives (e.g. doxycycline). [1]
ATC code J01 Antibacterials for systemic use is a therapeutic subgroup of the Anatomical Therapeutic Chemical Classification System, a system of alphanumeric codes developed by the World Health Organization (WHO) for the classification of drugs and other medical products.
The use of bacteria-derived tetracycline-inducible system permitting the switching on or off (Tet-On/Tet-Off system) [36] Targeted mutations by knock in gene and knock out sequence by using Cre-Lox recombination system [37] Introduction of retro viral mutations [38] Introduction of chemically induced mutations
Doxycycline has a high oral bioavailability, as it is almost completely absorbed in the stomach and proximal small intestine. [15] Unlike other tetracyclines, its absorption is not significantly affected by food or dairy intake. [15] However, co-administration of dairy products reduces the serum concentration of doxycycline by 20%. [15]
Skeletal formula of tetracycline with atoms and four rings numbered and labeled.. Tetracyclines are a group of broad-spectrum antibiotic compounds that have a common basic structure and are either isolated directly from several species of Streptomyces bacteria or produced semi-synthetically from those isolated compounds. [1]
The horizontal axis is the concentration of the ligand. As the Hill coefficient is increased, the saturation curve becomes steeper. In biochemistry and pharmacology, the Hill equation refers to two closely related equations that reflect the binding of ligands to macromolecules, as a function of the ligand concentration.
In biochemistry, control coefficients [1] are used to describe how much influence a given reaction step has on the flux or concentration of the species at steady state.This can be accomplished experimentally by changing the expression level of a given enzyme and measuring the resulting changes in flux and metabolite levels.
The solution of this differential equation is useful in calculating the concentration after the administration of a single dose of drug via IV bolus injection: = C t is concentration after time t; C 0 is the initial concentration (t=0) K is the elimination rate constant