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Consensus recommendations for trabecular meshwork cell isolation, characterization and culture.

Experimental eye research (2018-03-13)
Kate E Keller, Sanjoy K Bhattacharya, Theresa Borrás, Thomas M Brunner, Sunee Chansangpetch, Abbott F Clark, W Michael Dismuke, Yiqin Du, Michael H Elliott, C Ross Ethier, Jennifer A Faralli, Thomas F Freddo, Rudolf Fuchshofer, Michael Giovingo, Haiyan Gong, Pedro Gonzalez, Alex Huang, Murray A Johnstone, Paul L Kaufman, Mary J Kelley, Paul A Knepper, Casey C Kopczynski, John G Kuchtey, Rachel W Kuchtey, Markus H Kuehn, Raquel L Lieberman, Shan C Lin, Paloma Liton, Yutao Liu, Elke Lütjen-Drecoll, Weiming Mao, Marisse Masis-Solano, Fiona McDonnell, Colleen M McDowell, Darryl R Overby, Padmanabhan P Pattabiraman, Vijay K Raghunathan, P Vasanth Rao, Douglas J Rhee, Uttio Roy Chowdhury, Paul Russell, John R Samples, Donald Schwartz, Evan B Stubbs, Ernst R Tamm, James C Tan, Carol B Toris, Karen Y Torrejon, Janice A Vranka, Mary K Wirtz, Thomas Yorio, Jie Zhang, Gulab S Zode, Michael P Fautsch, Donna M Peters, Ted S Acott, W Daniel Stamer
RESUMEN

Cultured trabecular meshwork (TM) cells are a valuable model system to study the cellular mechanisms involved in the regulation of conventional outflow resistance and thus intraocular pressure; and their dysfunction resulting in ocular hypertension. In this review, we describe the standard procedures used for the isolation of TM cells from several animal species including humans, and the methods used to validate their identity. Having a set of standard practices for TM cells will increase the scientific rigor when used as a model, and enable other researchers to replicate and build upon previous findings.

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Sigma-Aldrich
Anticuerpo anti-miocilina (NT), clon 7.1, clone 7.1, from mouse
Sigma-Aldrich
Anti-Heterochromatin Protein-1 α Antibody, clone 2HP-2G9, ascites fluid, clone 2HP-2G9, Chemicon®