Mutations in the mitochondrial DNA cytochrome b gene (MTCYB) have been commonly associated with isolated mitochondrial myopathy and exercise intolerance, rarely with multisystem disorders, and only once with a parkinsonism/mitochondrial encephalomyopathy, lactic acidosis, and strokelike episodes (MELAS) overlap syndrome. Defects in MT-CYB are a rare cause of mitochondrial dysfunction underlying different myopathies. Defects in MTCYB are also found in cases of exercise intolerance accompanied by deafness, mental retardation, retinitis pigmentosa, cataract, growth retardation, epilepsy (multisystem disorder). Defects in MT-CYB are the cause of cardiomyopathy infantile histiocytoid (CMIH). Defects in MT-CYB contribute to Leber hereditary optic neuropathy (LHON).
Bovine Cytochrome b (MT-CYB) ELISA Kit employs a two-site sandwich ELISA to quantitate MT-CYB in samples. An antibody specific for MT-CYB has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and anyMT-CYB present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conjugated antibody specific for MT-CYB 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-CYB bound in the initial step. The color development is stopped and the intensity of the color is measured.
Bovine Cytochrome b (MT-CYB) 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.
bio-equip.cn
中文
