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Bio-FETs couple a transistor device with a bio-sensitive layer that can specifically detect bio-molecules such as nucleic acids and proteins. A Bio-FET system consists of a semiconducting field-effect transistor that acts as a transducer separated by an insulator layer (e.g. SiO 2) from the biological recognition element (e.g. receptors or probe molecules) which are selective to the target ...
The ratio of absorbance at 260 nm vs 280 nm is commonly used to assess DNA contamination of protein solutions, since proteins (in particular, the aromatic amino acids) absorb light at 280 nm. [ 2 ] [ 7 ] The reverse, however, is not true — it takes a relatively large amount of protein contamination to significantly affect the 260:280 ratio in ...
Biosensors used for screening combinatorial DNA libraries. In a biosensor, the bioreceptor is designed to interact with the specific analyte of interest to produce an effect measurable by the transducer. High selectivity for the analyte among a matrix of other chemical or biological components is a key requirement of the bioreceptor.
In rat liver, the total amount of NAD + and NADH is approximately 1 μmole per gram of wet weight, about 10 times the concentration of NADP + and NADPH in the same cells. [17] The actual concentration of NAD + in cell cytosol is harder to measure, with recent estimates in animal cells ranging around 0.3 mM , [ 18 ] [ 19 ] and approximately 1.0 ...
[10] While under standard conditions malate cannot reduce the more electronegative NAD +:NADH couple, in the cell the concentration of oxaloacetate is kept low enough that Malate dehydrogenase can reduce NAD + to NADH during the citric acid cycle. Fumarate + 2 H + + 2 e − → Succinate +0.03 [9] O 2 + 2H + + 2e − → H 2 O 2 +0.30
Biacore was founded in 1984 under the name of Pharmacia Biosensor AB, by researchers from Pharmacia, Linköping Institute of Technology and the Swedish National Defence Research Institute (FOA, now renamed the Swedish Defence Research Agency or FOI). The first Biacore SPR instrument was commercially released in 1990.
Nicotinamide adenine dinucleotide phosphate, abbreviated NADP [1] [2] or, in older notation, TPN (triphosphopyridine nucleotide), is a cofactor used in anabolic reactions, such as the Calvin cycle and lipid and nucleic acid syntheses, which require NADPH as a reducing agent ('hydrogen source').
In enzymology, a glutamate synthase (NADH) (EC 1.4.1.14) is an enzyme that catalyzes the chemical reaction. 2 L-glutamate + NAD + L-glutamine + 2-oxoglutarate + NADH + H + Glutamate synthase facilitates the ammonium assimilation pathway, which follows the enzymes, nitrite reductase and glutamine synthase. [1]