MNX1 encodes a nuclear protein, which contains a homeobox domain and is a transcription factor. Mutations in this gene result in Currarino syndrome, an autosomic dominant congenital malformation. Alternatively spliced transcript variants encoding different isoforms have been found for MNX1.
Human Motor neuron and pancreas homeobox protein 1 (MNX1) ELISA Kit employs a two-site sandwich ELISA to quantitate MNX1 in samples. An antibody specific for MNX1 has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and anyMNX1 present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conjugated antibody specific for MNX1 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 MNX1 bound in the initial step. The color development is stopped and the intensity of the color is measured.
Human Motor neuron and pancreas homeobox protein 1 (MNX1) 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-motor-neuron-and-pancreas-homeobox-protein-1-mnx1-elisa-kit-kte61575/
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