MT-ND4L (Mitochondrially Encoded NADH:Ubiquinone Oxidoreductase Core Subunit 4L) is a Protein Coding gene. Diseases associated with MT-ND4L include Leber Optic Atrophy and Mitochondrial Complex I Deficiency. Among its related pathways are Respiratory electron transport, ATP synthesis by chemiosmotic coupling, and heat production by uncoupling proteins. and Metabolism. GO annotations related to this gene include NADH dehydrogenase (ubiquinone) activity and oxidoreductase activity, acting on NAD(P)H. Core subunit of the mitochondrial membrane respiratory chain NADH dehydrogenase (Complex I) that is believed to belong to the minimal assembly required for catalysis. Complex I functions in the transfer of electrons from NADH to the respiratory chain. The immediate electron acceptor for the enzyme is believed to be ubiquinone (By similarity).
Human NADH-ubiquinone oxidoreductase chain 4L (MT-ND4L) ELISA Kit employs a two-site sandwich ELISA to quantitate MT-ND4L in samples. An antibody specific for MT-ND4L has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and anyMT-ND4L present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conjugated antibody specific for MT-ND4L is added to the wells. After washing, Streptavidin conjugated Horseradish Peroxidase (HRP) is added to the wells. Following a wash to remove any unbound avidin-enzyme reagent, a substrate solution is added to the wells and color develops in proportion to the amount of MT-ND4L bound in the initial step. The color development is stopped and the intensity of the color is measured.
Human NADH-ubiquinone oxidoreductase chain 4L (MT-ND4L) ELISA Kit listed herein is for research use only and is not intended for use in human or clinical diagnosis. Suggested applications of our products are not recommendations to use our products in violation of any patent or as a license. We cannot be responsible for patent infringements or other violations that may occur with the use of this product.
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