MFN2 encodes a mitochondrial membrane protein that participates in mitochondrial fusion and contributes to the maintenance and operation of the mitochondrial network. Mitofusin-2 is involved in the regulation of vascular smooth muscle cell proliferation, and it may play a role in the pathophysiology of obesity. Mutations in MFN2 cause Charcot-Marie-Tooth disease type 2A2, and hereditary motor and sensory neuropathy VI, which are both disorders of the peripheral nervous system. Defects in MFN2 have also been associated with early-onset stroke. Two transcript variants encoding the same protein have been identified.
Human Mitofusin-2 (MFN2) ELISA Kit employs a two-site sandwich ELISA to quantitate MFN2 in samples. An antibody specific for MFN2 has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and anyMFN2 present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conjugated antibody specific for MFN2 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 MFN2 bound in the initial step. The color development is stopped and the intensity of the color is measured.
Human Mitofusin-2 (MFN2) 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.
Find more details at http://www.abbkine.com/product/human-mitofusin-2-mfn2-elisa-kit-kte61636/
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