
NADPH-Cytochrome C Reductase Microplate Assay Kit
Please be informed that the price provided is for your reference only. For detailed pricing information, kindly reach out to our sales representative, Vecent.
Description
| SKU-Pack Size | Availability | Price |
abs580030-96T | 4 weeks | $670.00 |
Please be informed that the price provided is for your reference only. For detailed pricing information, kindly reach out to our sales representative, Vecent.
| Overview | |
| Synonym | NADPH-Cytochrome c Reductase; NCR |
| Applications | NADPH-Cytochrome c reductase activity can be detected and quantified through various methods. The measurement of this activity is important in understanding the functional role of the enzyme in cellular processes. To detect and quantify NADPH-Cytochrome c reductase activity, researchers typically follow a set of procedures. First, a sample containing the enzyme of interest is obtained. This can be done by extracting the enzyme from a specific tissue or by using recombinant techniques to express and purify the enzyme. Once the sample is prepared, the activity of NADPH-Cytochrome c reductase is measured using a suitable assay system. One commonly used assay is based on the reduction of cytochrome c by the enzyme. In this assay, cytochrome c serves as an electron acceptor, and its reduction can be monitored spectrophotometrically. To perform the assay, the sample is incubated with an appropriate concentration of cytochrome c and a source of NADPH, which is the electron donor for the enzyme. The reaction is allowed to proceed for a specific period, usually under optimized conditions such as pH and temperature. The progress of the reaction is monitored by measuring the change in absorbance of cytochrome c at a specific wavelength. To ensure the accuracy of the measurement, a control experiment is usually performed. This involves omitting either the enzyme sample or the NADPH, or both, to determine the background level of cytochrome c reduction. The activity of NADPH-Cytochrome c reductase is then calculated based on the rate of cytochrome c reduction over time. This is often expressed as units of enzyme activity per milligram of protein or per cell. In summary, the detection and quantification of NADPH-Cytochrome c reductase activity involve obtaining a sample, performing an assay using cytochrome c as a substrate, and calculating the enzyme activity. These methods provide valuable information about the activity of this enzyme and its role in cellular redox processes. |
| Properties | |
| Storage Temp. | Shipped and store at 4°C for 6 months. |
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