MYOC Antibody (monoclonal) (M01)
Mouse monoclonal antibody raised against a partial recombinant MYOC.
|Application ||WB, IHC, IP, E|
|Calculated MW||56972 Da|
|Other Names||Myocilin, Myocilin 55 kDa subunit, Trabecular meshwork-induced glucocorticoid response protein, Myocilin, N-terminal fragment, Myocilin 20 kDa N-terminal fragment, Myocilin, C-terminal fragment, Myocilin 35 kDa N-terminal fragment, MYOC, GLC1A, TIGR|
|Target/Specificity||MYOC (AAH29261, 36 a.a. ~ 135 a.a) partial recombinant protein with GST tag. MW of the GST tag alone is 26 KDa.|
|Format||Clear, colorless solution in phosphate buffered saline, pH 7.2 .|
|Storage||Store at -20°C or lower. Aliquot to avoid repeated freezing and thawing.|
|Precautions||MYOC Antibody (monoclonal) (M01) is for research use only and not for use in diagnostic or therapeutic procedures.|
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Provided below are standard protocols that you may find useful for product applications.
MYOC encodes the protein myocilin, which is believed to have a role in cytoskeletal function. MYOC is expressed in many occular tissues, including the trabecular meshwork, and was revealed to be the trabecular meshwork glucocorticoid-inducible response protein (TIGR). The trabecular meshwork is a specialized eye tissue essential in regulating intraocular pressure, and mutations in MYOC have been identified as the cause of hereditary juvenile-onset open-angle glaucoma.
Myocilin and optineurin coding variants in Hispanics of Mexican descent with POAG. McDonald KK, et al. J Hum Genet, 2010 Jul 29. PMID 20668460.Little evidence for association of the glaucoma gene MYOC with open-angle glaucoma. Sohn S, et al. Br J Ophthalmol, 2010 May. PMID 20447966.[Genetic variants of CYP1B1 and WDR36 in the patients with primary congenital glaucoma and primary open angle glaucoma from Saint-Petersburg] Motushchuk AE, et al. Genetika, 2009 Dec. PMID 20198978.Association of POAG risk factors and the Thr377Met MYOC mutation in an isolated Greek population. Wirtz MK, et al. Invest Ophthalmol Vis Sci, 2010 Jun. PMID 20107173.Variable clinical spectrum of the myocilin Gln368X mutation in a Dutch family with primary open angle glaucoma. Hogewind BF, et al. Curr Eye Res, 2010 Jan. PMID 20021252.
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