Please use this identifier to cite or link to this item: http://223.31.159.10:8080/jspui/handle/123456789/642
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dc.contributor.authorKumari, Aprajita-
dc.contributor.authorGupta, Alok Kumar-
dc.contributor.authorMishra, Sonal-
dc.contributor.authorWany, Aakanksha-
dc.contributor.authorGupta, Kapuganti Jagadis-
dc.date.accessioned2016-04-22T06:05:33Z-
dc.date.available2016-04-22T06:05:33Z-
dc.date.issued2016-
dc.identifier.citationMethods Mol. Biol., 1424: 31-38en_US
dc.identifier.isbn978-1-4939-3600-7-
dc.identifier.urihttp://172.16.0.77:8080/jspui/handle/123456789/642-
dc.descriptionAccepted date: 20 April 2016en_US
dc.description.abstractIn plants, nitrate reductase (NR) is a key enzyme that produces nitric oxide (NO) using nitrite as a substrate. Lower plants such as algae are shown to have nitric oxide synthase enzyme and higher plants contain NOS activity but enzyme responsible for NO production in higher plants is subjected to debate. In plant nitric oxide research, it is very important to measure NO very precisely in order to determine its functional role. A significant amount of NO is being scavenged by various cell components. The net NO production depends in production minus scavenging. Here, we describe methods to measure NO from purified NR and inducible nitric oxide synthase from mouse (iNOS), we also describe a method of measure NO scavenging by tobacco cell suspensions and mitochondria from roots.en_US
dc.language.isoen_USen_US
dc.publisherSpringeren_US
dc.subjectChemiluminescenceen_US
dc.subjectMitochondriaen_US
dc.subjectNitrate reductaseen_US
dc.subjectNitric oxide synthaseen_US
dc.subjectScavengingen_US
dc.titleNitric oxide measurement from purified enzymes and estimation of scavenging activity by gas phase chemiluminescence methoden_US
dc.typeBook chapteren_US
dc.identifier.officialurlhttp://link.springer.com/protocol/10.1007%2F978-1-4939-3600-7_3en_US
dc.identifier.doi10.1007/978-1-4939-3600-7_3en_US
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